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American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics

American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics

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中文名称：美国医学遗传学杂志,B部分。神经遗传学:官方出版的国际社会精神病遗传学

ISSN：1552-4841
出版周期：-

发文量：1214

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1.Mapping genes of complex psychiatric diseases in Daghestan genetic isolates.

机译：达格斯坦遗传分离物中复杂精神疾病的基因定位。
- 作者：Bulayeva KB;Leal SM;Pavlova TA;Kurbanov RM;Glatt SJ;Bulayev OA;Tsuang MT
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Genetic Predisposition to Disease;
- Mental Disorders;
- 疾病遗传易感性;
- 精神障碍;
2.Linkage disequilibrium analysis in the LOC93081-KDELC1-BIVM region on 13q in bipolar disorder.

机译：双相情感障碍中13q的LOC93081-KDELC1-BIVM区域的连锁不平衡分析。
- 作者：Ferraren DO;Liu C;Badner JA;Corona W;Rezvani A;Monje VD;Gershon ES;Bonner TI;Detera Wadleigh SD
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Bipolar Disorder;
- Chromosomes;
- Human;
- Pair 13;
- Linkage Disequilibrium;
- Polymorphism;
- Single Nucleotide;
- 双相情感性精神病;
- 染色体;
- 人;
- 13对;
- 连锁不平衡;
3.Serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder in Chinese Han subjects.

机译：5-羟色胺5-HT1B受体基因与中国汉族人群注意缺陷多动障碍。
- 作者：Li J;Wang Y;Zhou R;Zhang H;Yang L;Wang B;Khan S;Faraone SV
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Attention Deficit Disorder with Hyperactivity;
- Receptor;
- Serotonin;
- 5-HT1B;
- 轻微脑损伤综合征;
4.The 3111T/C polymorphism of hClock is associated with evening preference and delayed sleep timing in a Japanese population sample.

机译：hClock的3111T / C多态性与日本人群样本中的夜间偏好和延迟的睡眠时间有关。
- 作者：Mishima K;Tozawa T;Satoh K;Saitoh H;Mishima Y
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Circadian Rhythm;
- Polymorphism;
- Single Nucleotide;
- Sleep;
- Trans-Activators;
- 昼夜节律;
- 睡眠;
- 反式作用因子;
5.Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia.

机译：reelin基因与精神分裂症的5'UTR多态性的基于人群和基于家庭的关联研究。
- 作者：Goldberger C;Gourion D;Leroy S;Schurhoff F;Bourdel MC;Leboyer M;Krebs MO
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
6.Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease.

机译：定义帕金森氏病两个不同家族的帕金外显子4缺失末端。
- 作者：Clarimon J;Johnson J;Dogu O;Horta W;Khan N;Lees AJ;Hardy J;Singleton A
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Exons;
- Gene Deletion;
- Parkinson Disease;
- Ubiquitin-Protein Ligases;
- 外显子;
- 基因缺失;
- 帕金森病;
7.Chromosome 19p13 loci in Finnish migraine with aura families.

机译：芬兰偏头痛中带有先兆家族的19p13染色体位点。
- 作者：Kaunisto MA;Tikka PJ;Kallela M;Leal SM;Papp JC;Korhonen A;Hamalainen E;Harno H;Havanka H;Nissila M;Sako E;Ilmavirta M;Kaprio J;Farkkila M;Ophoff RA;Palotie A;Wessman M
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Chromosomes;
- Human;
- Pair 19;
- Migraine with Aura;
- 染色体;
- 人;
- 19对;
8.APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation.

机译：APOE和其他基因座会通过PS2突变影响阿尔茨海默氏病家族的发病年龄。
- 作者：Wijsman EM;Daw EW;Yu X;Steinbart EJ;Nochlin D;Bird TD;Schellenberg GD
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Alzheimer Disease;
- Apolipoproteins E;
- Membrane Proteins;
- Mutation;
- 载脂蛋白E类;
- 膜蛋白质类;
- 突变;
9.Evidence for the gamma-amino-butyric acid type B receptor 1 (GABBR1) gene as a susceptibility factor in obsessive-compulsive disorder.

机译：证据表明，γ-氨基丁酸B型受体1（GABBR1）基因是强迫症中的易感因素。
- 作者：Zai G;Arnold P;Burroughs E;Barr CL;Richter MA;Kennedy JL
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Genetic Predisposition to Disease;
- Obsessive-Compulsive Disorder;
- Receptors;
- GABA-B;
- 疾病遗传易感性;
- 强迫性障碍;
- 受体;
- GABA-B;
10.Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder.

机译：注意力缺陷多动障碍中人NR4A2多态性的鉴定和表征。
- 作者：Smith KM;Bauer L;Fischer M;Barkley R;Navia BA
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
11.Sequence variants of the DRD4 gene in autism: further evidence that rare DRD4 7R haplotypes are ADHD specific.

机译：自闭症中DRD4基因的序列变体：进一步的证据表明罕见的DRD4 7R单倍型是ADHD特异性的。
- 作者：Grady DL;Harxhi A;Smith M;Flodman P;Spence MA;Swanson JM;Moyzis RK
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Autistic Disorder;
- Receptors;
- Dopamine D2;
- 孤独性障碍;
- 受体;
- 多巴胺D2;
12.DNA pooling analysis of ADHD and genes regulating vesicle release of neurotransmitters.

机译：ADHD的DNA合并分析和调节神经递质的囊泡释放的基因。
- 作者：Brookes KJ;Knight J;Xu X;Asherson P
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Attention Deficit Disorder with Hyperactivity;
- Cytoplasmic Vesicles;
- DNA;
- 轻微脑损伤综合征;
- 基因库;
- 神经递质药;
- 突触;
13.The biography of psychiatric genetics: from early achievements to historical burden, from an anxious society to critical geneticists.

机译：精神遗传学传记：从早期的成就到历史的负担，从焦虑的社会到批判的遗传学家。
- 作者：Propping P
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Genetics;
- Behavioral;
- Psychiatry;
- 遗传学;
- 行为;
- 精神病学;
14.No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample.

机译：在酒精中毒样本遗传学的合作研究中，第5号染色体上的GABAA受体基因与酒精中毒没有关联。
- 作者：Dick DM;Edenberg HJ;Xuei X;Goate A;Hesselbrock V;Schuckit M;Crowe R;Foroud T
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Alcoholism;
- Chromosomes;
- Human;
- Pair 5;
- Receptors;
- GABA-A;
- 酒精中毒;
- 染色体;
- 人;
- 5对;
- 受体;
- GABA-A;
15.Serotonin transporter promoter polymorphism and monoamine oxidase type A VNTR allelic variants together influence alcohol binge drinking risk in young women.

机译：血清素转运蛋白启动子多态性和A型单胺氧化酶VNTR等位基因变异共同影响年轻女性酗酒的饮酒风险。
- 作者：Herman AI;Kaiss KM;Ma R;Philbeck JW;Hasan A;Dasti H;DePetrillo PB
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
16.Exclusion of non-synonymous SNPs and a polyglutamine tract in SMRT/N-CoR2 as common deleterious mutation for bipolar disorder in the Sagnenay-Lac-St-Jean population.

机译：Sagnenay-Lac-St-Jean人群中双相情感障碍的常见有害突变被SMRT / N-CoR2中的非同义SNP和多聚谷氨酰胺排除。
- 作者：Shink E;Harvey M;Tremblay M;Raymond C;Labbe M;Gagne B;Barden N
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Bipolar Disorder;
- DNA-Binding Proteins;
- Mutation;
- Polymorphism;
- Single Nucleotide;
- 双相情感性精神病;
- DNA结合蛋白质类;
- 突变;
- 阻遏蛋白质类;
- 三核苷酸重复;
17.DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch families.

机译：在荷兰家庭中，DAT1，DRD4和DRD5多态性与ADHD不相关。
- 作者：Bakker SC;van der Meulen EM;Oteman N;Schelleman H;Pearson PL;Buitelaar JK;Sinke RJ
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Attention Deficit Disorder with Hyperactivity;
- Polymorphism;
- Genetic;
- 轻微脑损伤综合征;
18.Brain perfusion and dopaminergic genes in boys with attention-deficit/hyperactivity disorder.

机译：注意缺陷/多动症男孩的脑灌注和多巴胺能基因。
- 作者：Szobot C;Roman T;Cunha R;Acton P;Hutz M;Rohde LA
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Brain;
- Membrane Glycoproteins;
- Membrane Transport Proteins;
- Nerve Tissue Proteins;
- 脑;
- 膜糖蛋白类;
- 神经组织蛋白质类;
- 受体;
- 多巴胺D2;
19.Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.

机译：基因组筛查会影响发病年龄的基因座以及晚期阿尔茨海默氏病发病率的下降速率。
- 作者：Holmans P;Hamshere M;Hollingworth P;Rice F;Tunstall N;Jones S;Moore P;Wavrant DeVrieze F;Myers A;Crook R;Compton D;Marshall H;Meyer D;Shears S;Booth J;Ramic D;Williams N;Norton N;Abraham R;Kehoe P;Williams H;Rudrasingham V;ODonov
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Alzheimer Disease;
- Genetic Predisposition to Disease;
- Genome;
- Human;
- 疾病遗传易感性;
- 基因组;
- 人;
20.Selection of eating-disorder phenotypes for linkage analysis.

机译：选择进食障碍表型进行连锁分析。
- 作者：Bulik CM;Bacanu SA;Klump KL;Fichter MM;Halmi KA;Keel P;Kaplan AS;Mitchell JE;Rotondo A;Strober M;Treasure J;Woodside DB;Sonpar VA;Xie W;Bergen AW;Berrettini WH;Kaye WH;Devlin B
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Eating Disorders;
- Linkage (Genetics);
- 进食障碍;
- 连锁(遗传学);
21.Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates.

机译：使用选定的行为表型作为定量特征或协变量，对厌食症和神经性贪食症人群进行连锁分析。
- 作者：Bacanu SA;Bulik CM;Klump KL;Fichter MM;Halmi KA;Keel P;Kaplan AS;Mitchell JE;Rotondo A;Strober M;Treasure J;Woodside DB;Sonpar VA;Xie W;Bergen AW;Berrettini WH;Kaye WH;Devlin B
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Anorexia Nervosa;
- Bulimia Nervosa;
- Linkage (Genetics);
- Phenotype;
- Quantitative Trait Loci;
- 厌食;
- 神经性;
- 连锁(遗传学);
- 表型;
22.Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.

机译：大型退伍军人事务合作研究样本中的精神分裂症家庭的基因组扫描：与18p11.32连锁以及6号和14号染色体种族异质性的证据。
- 作者：Faraone SV;Skol AD;Tsuang DW;Young KA;Haverstock SL;Prabhudesai S;Mena F;Menon AS;Leong L;Sautter F;Baldwin C;Bingham S;Weiss D;Collins J;Keith T;Vanden Eng JL;Boehnke M;Tsuang MT;Schellenberg GD
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- African Americans;
- Chromosomes;
- Human;
- Pair 18;
- European Continental Ancestry Group;
- 染色体;
- 人;
- 18对;
- 基因组;
- 人;
- 连锁(遗传学);
- 精神分裂症;
23.Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletion.

机译：具有新颖的17p12p13.1缺失的儿童具有出色的语言表达能力和非语言学习障碍。
- 作者：Steele DL;Chisholm AK;McGhie JD;Gardner RJ;Scheffer IE;Slater HR;Dawson G
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Chromosome Deletion;
- Chromosomes;
- Human;
- Pair 17;
- Language Development;
- Learning Disorders;
- 染色体;
- 人;
- 17对;
- 语言发展;
- 学习障碍;
24.Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B.

机译：与注意力缺陷多动障碍（ADHD）相关的五个候选基因的等位基因定量性状基因座分析：DRD4，DAT1，DRD5，SNAP-25和5HT1B。
- 作者：Mill J;Xu X;Ronald A;Curran S;Price T;Knight J;Craig I;Sham P;Plomin R;Asherson P
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
25.Haplotype diversity and somatic instability in normal and expanded SCA8 alleles.

机译：正常和扩展SCA8等位基因中的单倍型多样性和体细胞不稳定性。
- 作者：Martins S;Seixas AI;Magalhaes P;Coutinho P;Sequeiros J;Silveira I
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
26.Association between the DRD2 A1 allele and opium addiction in the Iranian population.

机译：伊朗人口中DRD2 A1等位基因与鸦片成瘾之间的关联。
- 作者：Shahmoradgoli Najafabadi M;Ohadi M;Joghataie MT;Valaie F;Riazalhosseini Y;Mostafavi H;Mohammadbeigi F;Najmabadi H
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Opium;
- Receptors;
- Dopamine D2;
- Substance-Related Disorders;
- 受体;
- 多巴胺D2;
- 物质相关性障碍;
27.Taiwan schizophrenia linkage study: the field study.

机译：台湾精神分裂症连锁研究：实地研究。
- 作者：Hwu HG;Faraone SV;Liu CM;Chen WJ;Liu SK;Shieh MH;Hwang TJ;Tsuang MM;OuYang WC;Chen CY;Chen CC;Lin JJ;Chou FH;Chueh CM;Liu WM;Hall MH;Tsuang MT
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Schizophrenia;
- 精神分裂症;
28.New Huntington disease mutation arising from a paternal CAG34 allele showing somatic length variation in serially passaged lymphoblasts.

机译：由父系CAG34等位基因引起的新的亨廷顿病突变，在连续传代的淋巴母细胞中显示出体长变化。
- 作者：Cannella M;Maglione V;Martino T;Simonelli M;Ragona G;Squitieri F
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
29.Relationship of MAO-A promoter (u-VNTR) and COMT (V158M) gene polymorphisms to CSF monoamine metabolites levels in a psychiatric sample of caucasians: A preliminary report.

机译：白人精神病学样本中MAO-A启动子（u-VNTR）和COMT（V158M）基因多态性与CSF单胺代谢产物水平的关系：初步报告。
- 作者：Zalsman G;Huang YY;Harkavy Friedman JM;Oquendo MA;Ellis SP;Mann JJ
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
30.No association of a non-synonymous PLAU polymorphism with Alzheimer's disease and disease-related traits.

机译：没有同义的PLAU多态性与阿尔茨海默氏病和疾病相关性状的关联。
- 作者：Papassotiropoulos A;Tsolaki M;Wollmer MA;Molyva D;Thal DR;Huynh KD;Tracy J;Staehelin HB;Monsch AU;Nitsch RM;Hock C
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Alzheimer Disease;
- Polymorphism;
- Single Nucleotide;
- Urinary Plasminogen Activator;
31.Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus.

机译：在MJD1 / SCA3位点鉴定与疾病表型相关的新型45个重复的不稳定等位基因。
- 作者：Padiath QS;Srivastava AK;Roy S;Jain S;Brahmachari SK
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Machado-Joseph Disease;
- Nerve Tissue Proteins;
- Trinucleotide Repeats;
- Machado-Joseph病;
- 神经组织蛋白质类;
- 三核苷酸重复;
32.Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblings.

机译：在选定的兄弟姐妹社区样本中，单胺基因与抑郁和焦虑程度的关联分析。
- 作者：Nash MW;Sugden K;Huezo Diaz P;Williamson R;Sterne A;Purcell S;Sham PC;Craig IW
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Anxiety Disorders;
- Depressive Disorder;
- Genetic Predisposition to Disease;
- 焦虑症;
- 抑郁障碍;
- 疾病遗传易感性;
33.Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.

机译：脑源性神经营养因子基因（BDNF）的突变筛查：对肥胖，进食障碍和注意力不足/多动障碍患者的几种遗传变异的鉴定和关联研究。
- 作者：Friedel S;Horro FF;Wermter AK;Geller F;Dempfle A;Reichwald K;Smidt J;Bronner G;Konrad K;Herpertz Dahlmann B;Warnke A;Hemminger U;Linder M;Kiefl H;Goldschmidt HP;Siegfried W;Remschmidt H;Hinney A;Hebebrand J
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Brain-Derived Neurotrophic Factor;
- Mutation;
- 脑源性神经营养因子;
- 突变;
34.Insomnia improvement during antidepressant treatment and CLOCK gene polymorphism.

机译：抗抑郁药治疗期间失眠改善和CLOCK基因多态性。
- 作者：Serretti A;Cusin C;Benedetti F;Mandelli L;Pirovano A;Zanardi R;Colombo C;Smeraldi E
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Antidepressive Agents;
- Mood Disorders;
- Polymorphism;
- Genetic;
- Sleep Initiation and Maintenance Disorders;
- 抗抑郁药;
- 情绪障碍;
- 反式作用因子;
35.Mutational screening and association study of glutamate decarboxylase 1 as a candidate susceptibility gene for bipolar affective disorder and schizophrenia.

机译：谷氨酸脱羧酶1作为双相情感障碍和精神分裂症候选易感基因的突变筛选和关联研究。
- 作者：Lundorf MD;Buttenschon HN;Foldager L;Blackwood DH;Muir WJ;Murray V;Pelosi AJ;Kruse TA;Ewald H;Mors O
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
36.Cytosolic PLA2 genes possibly contribute to the etiology of schizophrenia.

机译：胞质PLA2基因可能有助于精神分裂症的病因。
- 作者：Tao R;Yu Y;Zhang X;Guo Y;Shi J;Zhang X;Xie L;Liu S;Ju G;Xu Q;Shen Y;Wei J
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Isoenzymes;
- Phospholipases A;
- Polymorphism;
- Single Nucleotide;
- Schizophrenia;
- 同工酶类;
- 磷脂酶A类;
- 精神分裂症;
37.Linkage to chromosome 14q in Alzheimer's disease (AD) patients without psychotic symptoms.

机译：无精神病症状的阿尔茨海默氏病（AD）患者与14q染色体的连锁。
- 作者：Avramopoulos D;Fallin MD;Bassett SS
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Alzheimer Disease;
- Chromosomes;
- Human;
- Pair 14;
- 染色体;
- 人;
- 14对;
38.Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders.

机译：全基因组连锁分析扩展了犹他州的谱系，确定了影响复发，早发的重大抑郁症和焦虑症的基因座。
- 作者：Camp NJ;Lowry MR;Richards RL;Plenk AM;Carter C;Hensel CH;Abkevich V;Skolnick MH;Shattuck D;Rowe KG;Hughes DC;Cannon Albright LA
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Anxiety Disorders;
- Depressive Disorder;
- Genetic Predisposition to Disease;
- 焦虑症;
- 抑郁障碍;
- 疾病遗传易感性;
- 基因组;
- 人;
- 连锁(遗传学);
39.Transmission disequilibrium suggests a role for the sulfotransferase-4A1 gene in schizophrenia.

机译：传输不平衡表明磺基转移酶-4A1基因在精神分裂症中起作用。
- 作者：Brennan MD;Condra J
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Linkage Disequilibrium;
- Schizophrenia;
- Sulfotransferases;
- 精神分裂症;
- 磺基转移酶类;
40.Association between BDNF val66 met genotype and episodic memory.

机译：BDNF val66满足基因型和情景记忆之间的关联。
- 作者：Dempster E;Toulopoulou T;McDonald C;Bramon E;Walshe M;Filbey F;Wickham H;Sham PC;Murray RM;Collier DA
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Brain-Derived Neurotrophic Factor;
- Memory;
- Polymorphism;
- Single Nucleotide;
- 脑源性神经营养因子;
- 记忆;
41.Familial cognitive deficits in schizophrenia.

机译：精神分裂症的家族性认知缺陷。
- 作者：Hoff AL;Svetina C;Maurizio AM;Crow TJ;Spokes K;DeLisi LE
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Cognition Disorders;
- Schizophrenia;
- 认知障碍;
- 精神分裂症;
42.Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families.

机译：台湾家庭中精神分裂症与染色体8p21上神经调节蛋白1基因附近基因座的联系证据。
- 作者：Liu CM;Hwu HG;Fann CS;Lin CY;Liu YL;Ou Yang WC;Lee SF
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Chromosomes;
- Human;
- Pair 8;
- Genetic Predisposition to Disease;
- Neuregulin-1;
- 染色体;
- 人;
- 8对;
- 疾病遗传易感性;
- 精神分裂症;
43.No association of GSK3beta gene (GSK3B) with Japanese schizophrenia.

机译：GSK3beta基因（GSK3B）与日本精神分裂症没有关联。
- 作者：Ikeda M;Iwata N;Suzuki T;Kitajima T;Yamanouchi Y;Kinoshita Y;Ozaki N
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Glycogen Synthase Kinase 3;
- Schizophrenia;
- 精神分裂症;
44.5-HT 1A polymorphism and self-transcendence in mood disorders.

机译：5-HT 1A多态性和自我超越在情绪障碍中。
- 作者：Lorenzi C;Serretti A;Mandelli L;Tubazio V;Ploia C;Smeraldi E
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Mood Disorders;
- Polymorphism;
- Genetic;
- Receptor;
- Serotonin;
- 5-HT1A;
- 情绪障碍;
45.Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): increased prevalence of the 2-repeat allele.

机译：多动胺受体D4（DRD4）基因在中国汉族儿童的注意缺陷/多动症（ADHD）：2重复等位基因的患病率增加。
- 作者：Leung PW;Lee CC;Hung SF;Ho TP;Tang CP;Kwong SL;Leung SY;Yuen ST;Lieh Mak F;Oosterlaan J;Grady D;Harxhi A;Ding YC;Chi HC;Flodman P;Schuck S;Spence MA;Moyzis R;Swanson J
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Attention Deficit Disorder with Hyperactivity;
- Receptors;
- Dopamine D2;
- 轻微脑损伤综合征;
- 受体;
- 多巴胺D2;
46.Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's Disease.

机译：人脑衍生的神经营养因子（BDNF）基因，剪接模式以及与药物滥用和帕金森氏病相关性的评估。
- 作者：Liu QR;Walther D;Drgon T;Polesskaya O;Lesnick TG;Strain KJ;de Andrade M;Bower JH;Maraganore DM;Uhl GR
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
47.Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder.

机译：确认脑源性神经营养因子（BDNF）基因中的Val66Met多态性与双相性I型障碍之间的关联。
- 作者：Lohoff FW;Sander T;Ferraro TN;Dahl JP;Gallinat J;Berrettini WH
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Bipolar Disorder;
- Brain-Derived Neurotrophic Factor;
- Polymorphism;
- Genetic;
- 双相情感性精神病;
- 脑源性神经营养因子;
- 缬氨酸;
48.Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.

机译：载脂蛋白E4可能是帕金森氏病19号染色体连锁峰的原因。
- 作者：Martinez M;Brice A;Vaughan JR;Zimprich A;Breteler MM;Meco G;Filla A;Farrer MJ;Betard C;Singleton A;Hardy J;De Michele G;Bonifati V;Oostra BA;Gasser T;Wood NW;Durr A
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Apolipoproteins E;
- Chromosomes;
- Human;
- Pair 19;
- Linkage (Genetics);
- Parkinson Disease;
- 载脂蛋白E类;
- 染色体;
- 人;
- 19对;
- 连锁(遗传学);
- 帕金森病;
49.Linkage and candidate gene analysis of 14q22-24 in bipolar disorder: support for GCHI as a novel susceptibility gene.

机译：双相情感障碍中14q22-24的连锁和候选基因分析：支持GCHI作为新的易感基因。
- 作者：Kealey C;Roche S;Claffey E;McKeon P
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
- Bipolar Disorder;
- Chromosomes;
- Human;
- Pair 14;
- GTP Cyclohydrolase;
- Genetic Predisposition to Disease;
- 双相情感性精神病;
- 染色体;
- 人;
- 14对;
- GTP环化水解酶;
- 疾病遗传易感性;
- 连锁(遗传学);
50.Molecular genetic studies of ADHD: 1991 to 2004.

机译：多动症的分子遗传学研究：1991年至2004年。
- 作者：Bobb AJ;Castellanos FX;Addington AM;Rapoport JL
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2005年第1期
51.PCM1 and schizophrenia: A replication study in the northern Swedish population

机译：PCM1和精神分裂症：在瑞典北部人群中的复制研究
- 作者：MoensL.N.;CeulemansS.;AlaertsM.;VanDenBosscheM.J.A.;LenaertsA.-S.;DeZutterS.;NorrbackK.-F.;AdolfssonR.;Del-FaveroJ.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第6期
- Association;
- DISC1 pathway;
- PCM1;
- Replication;
- Schizophrenia;
52.Are recently identified genetic variants regulating BMI in the general population associated with anorexia nervosa?

机译：最近确定的一般人群中调节BMI的遗传变异与神经性厌食症有关吗？
- 作者：BrandysM.K.;VanElburgA.A.;LoosR.J.F.;BauerF.;HendriksJ.;VanDerSchouwY.T.;AdanR.A.H.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Eating disorders;
- Gene association;
- Logistic regression;
- Premorbid BMI;
- Risk factors;
53.Compulsivity in mouse strains homologous with chromosomes 7p and 15q linked to obsessive-compulsive disorder

机译：与强迫症有关的与7p和15q染色体同源的小鼠品系的强迫性
- 作者：KasM.J.H.;GelegenC.;VanNieuwerburghF.;WestenbergH.G.M.;DeforceD.;DenysD.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Animal model;
- Behavior;
- Endophenotype;
- Genetics;
- Psychiatry;
54.Quantitative analysis of alternative transcripts of human PCDH11X/Y genes

机译：人类PCDH11X / Y基因替代转录本的定量分析
- 作者：AhnK.;HuhJ.-W.;KimD.-S.;HaH.-S.;KimY.-J.;LeeJ.-R.;KimH.-S.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第3期
- Alternative transcripts;
- Brain disorders;
- Gene expression;
- Human brain;
- PCDH11X/Y;
- Real-time RT-PCR;
55.Nucleotide variation in central nervous system genes among male suicide attempters

机译：男性自杀未遂者中枢神经系统基因的核苷酸变异
- 作者：Baca-GarciaE.;Vaquero-LorenzoC.;Perez-RodriguezM.M.;GratacòsM.;BayésM.;Santiago-MozosR.;Leiva-MurilloJ.M.;DePrado-CumplidoM.;Artes-RodriguezA.;CeverinoA.;Diaz-SastreC.;Fernandez-NavarroP.;CostasJ.;Fernandez-PiquerasJ.;Diaz-HernandezM.;DeLeonJ.;Baca-BaldomeroE.;Saiz-RuizJ.;MannJ.J.;ParseyR.V.;CarracedoA.;EstivillX.;OquendoM.A.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Glutamate receptors;
- Sensitivity and specificity;
- Serotonin receptors;
- Single nucleotide polymorphism;
- Statistical models;
56.An association between Epac-1 gene variants and anxiety and depression in two independent samples

机译：Epac-1基因变异与两个独立样本中的焦虑和抑郁之间的关联
- 作者：MiddeldorpC.M.;VinkJ.M.;HettemaJ.M.;DeGeusE.J.C.;KendlerK.S.;WillemsenG.;NealeM.C.;BoomsmaD.I.;ChenX.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Anxiety;
- Association study;
- Depression;
- RapGEF-3;
57.Autistic traits in simplex and multiplex autism families: Focus on unaffected relatives

机译：单纯性和多重性自闭症家庭的自闭症特征：关注未受影响的亲戚
- 作者：HoekstraR.A.;WheelwrightS.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
58.Risk variants in the S100B gene predict elevated S100B serum concentrations in healthy individuals

机译：S100B基因的风险变异预测健康个体中S100B血清浓度升高
- 作者：HohoffC.;PonathG.;FreitagC.M.;K?stnerF.;KrakowitzkyP.;DomschkeK.;KoelkebeckK.;KippF.;VonEiffC.;DeckertJ.;RothermundtM.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Association;
- Functional polymorphisms;
- mRNA expression;
- Postmortem frontal cortex;
- S100 calcium binding protein b;
59.Effect of dopamine transporter gene (SLC6A3) variation on dorsal anterior cingulate function in attention-deficit/hyperactivity disorder

机译：多巴胺转运蛋白基因（SLC6A3）变异对注意力不足/多动障碍中背扣带功能的影响
- 作者：BrownA.B.;BiedermanJ.;ValeraE.M.;DoyleA.E.;BushG.;SpencerT.;MonuteauxM.C.;MickE.;Whitfield-GabrieliS.;MakrisN.;LaVioletteP.S.;Oscar-BermanM.;FaraoneS.V.;SeidmanL.J.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- adhd;
- Anterior cingulate;
- Dopamine transporter gene;
- Functional magnetic resonance imaging;
- Genetics;
60.Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression.

机译：类固醇硫酸酯酶（STS）基因的多态性与注意力缺陷多动障碍有关，并影响脑组织mRNA表达。
- 作者：Brookes KJ;Hawi Z;Park J;Scott S;Gill M;Kent L
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第8期
61.Methylation at SLC6A4 is linked to family history of child abuse: An examination of the Iowa adoptee sample

机译：SLC6A4的甲基化与虐待儿童的家族史有关：对爱荷华州收养者样本的检查
- 作者：BeachS.R.H.;BrodyG.H.;TodorovA.A.;GunterT.D.;PhilibertR.A.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
62.The impact of a genome-wide supported psychosis variant in the ZNF804A gene on memory function in schizophrenia.

机译：ZNF804A基因中全基因组支持的精神病变体对精神分裂症记忆功能的影响。
- 作者：Hashimoto R;Ohi K;Yasuda Y;Fukumoto M;Iwase M;Iike N;Azechi M;Ikezawa K;Takaya M;Takahashi H;Yamamori H;Okochi T;Tanimukai H;Tagami S;Morihara T;Okochi M;Tanaka T;Kudo T;Kazui H;Iwata N;Takeda M
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第8期
63.Psychiatric and behavioral manifestations of lysosomal storage disorders.

机译：溶酶体贮积症的精神病学和行为表现。
- 作者：Staretz Chacham O;Choi JH;Wakabayashi K;Lopez G;Sidransky E
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第7期
64.Behavioral phenotype in the 9q subtelomeric deletion syndrome: A report about two adult patients

机译：9q亚端粒缺失综合征的行为表型：两名成人患者的报告。
- 作者：VerhoevenW.M.A.;KleefstraT.;EggerJ.I.M.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- 9qSTDS;
- Apathy;
- Behavioral phenotype;
- Mental retardation;
- Sleep disturbances;
65.Psychiatric syndromes in individuals with chromosome 18 abnormalities

机译：18号染色体异常个体的精神病综合症
- 作者：ZavalaJ.;RamirezM.;MedinaR.;HeardP.;CarterE.;CrandallA.;HaleD.;CodyJ.;EscamillaM.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第3期
- 18p;
- 18q;
- Deletions;
- Psychiatric disorders;
- Tetrasomy;
66.Identical but not the same: The value of discordant monozygotic twins in genetic research

机译：相同但不相同：不一致的单卵双胞胎在遗传研究中的价值
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第6期
- Chromosome disorders;
- Discordant;
- Genetic diseases;
- Inborn;
- Monozygotic;
- Twin studies;
- Twins;
67.Intra-individual variability in genetic and environmental models of attention-deficit/ hyperactivity disorder

机译：注意缺陷/多动障碍的遗传和环境模型中的个体内变异
- 作者：PerryG.M.L.;SagvoldenT.;FaraoneS.V.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第5期
- Hyperactivity;
- IIV;
- Impulsiveness;
- Inattention;
- Spontaneous hypertensive rat;
68.Genome-scan for bipolar disorder with sib-pair families in the Sardinian population: A new susceptibility locus on chromosome 1p22-p21?

机译：撒丁岛人群中具有同胞对家族的躁郁症的基因组扫描：1p22-p21染色体上的新易感基因座？
- 作者：DelZompoM.;SeverinoG.;ArdauR.;ChillottiC.;PiccardiM.;DibC.;MuzardG.;SoubigouS.;DerockM.;FournelR.;VaubienY.;RocheS.;Bowen-SquiresL.;GéninE.;CousinE.;DeleuzeJ.-F.;FauconBiguetN.;MalletJ.;MeloniR.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第6期
- Isolated population;
- NPL scores;
- Suggestive linkage;
69.Association and interaction analysis of variants in CHRNA5/CHRNA3/CHRNB4 gene cluster with nicotine dependence in African and European Americans

机译：非洲裔和欧洲裔美国人中CHRNA5 / CHRNA3 / CHRNB4基因簇变异与尼古丁依赖性的关联和相互作用分析
- 作者：LiM.D.;XuQ.;LouX.-Y.;PayneT.J.;NiuT.;MaJ.Z.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第3期
- Association analysis;
- CHRNA3;
- CHRNA5;
- CHRNB4;
- Interaction analysis;
- Nicotine dependence;
- Smoking;
70.Analysis of the micro-RNA-133 and PITX3 genes in Parkinson's disease

机译：帕金森氏病中微小RNA-133和PITX3基因的分析
- 作者：DeMenaL.;CotoE.;CardoL.F.;DíazM.;BlázquezM.;RibacobaR.;SalvadoC.;PastorP.;SamaranchL.;MorisG.;MenéndezM.;CoraoA.I.;AlvarezV.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第6期
- Dna polymorphisms;
- Genetic risk;
- Micro rnas;
- Parkinson's disease;
71.Association study of PD E4B gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case - control samples

机译：PD E4B基因变异在斯堪的纳维亚精神分裂症和双相情感障碍多中心病例对照中的关联研究
- 作者：K?hlerA.K.;Otn?ssM.K.;WirgenesK.V.;HansenT.;J?nssonE.G.;AgartzI.;HallH.;WergeT.;MorkenG.;MorsO.;MellerupE.;DamH.;KoefodP.;MelleI.;SteenV.M.;AndreassenO.A.;DjurovicS.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Candidate gene;
- Genetic association;
- PDE4B isoform;
- PDE4B3;
- Psychotic disorder;
72.High frequency of multiexonic deletion of the GCH1 gene in a Taiwanese cohort of dopa-response dystonia

机译：台湾多巴反应性肌张力障碍人群中GCH1基因的多外显子缺失频率很高
- 作者：Wu-ChouY.-H.;YehT.-H.;WangC.-Y.;LinJ.-J.;HuangC.-C.;ChangH.-C.;LaiS.-C.;ChenR.-S.;WengY.-H.;HuangC.-L.;LuC.-S.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第4期
- GCH1 deletion;
- MLPA;
- qPCR;
- Segawa's disease;
73.Dizziness genes

机译：头晕基因
- 作者：SandP.G.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第6期
74.Association of CHRN genes with 'dizziness' to tobacco

机译：CHRN基因与烟草“头晕”的关联
- 作者：EhringerM.A.;McQueenM.B.;HoftN.R.;SacconeN.L.;StitzelJ.A.;WangJ.C.;BierutL.J.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Gene expression;
- Genetics;
- Humans;
- Nicotinic receptors;
- Subjective effects;
- Tobacco;
75.NRG1 gene in recurrent major depression: No association in a large-scale case - Control association study

机译：复发性重度抑郁症中的NRG1基因：在大型病例中无关联-对照关联研究
- 作者：SchosserA.;Cohen-WoodsS.;GaysinaD.;ChowP.C.;MartucciL.;FarmerA.;KorszunA.;GunashingheC.;GrayJ.;JonesL.;CraddockN.;OwenM.J.;CraigI.W.;McGuffinP.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Affective disorders;
- Association;
- Depression;
- NRG1;
76.The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder.

机译：双相关联病例对照研究（BACCS）和荟萃分析：与5,10-亚甲基四氢叶酸还原酶基因和双相情感障碍无关联。
- 作者：Cohen Woods S;Craig I;Gaysina D;Gray J;Gunasinghe C;Craddock N;Elkin A;Jones L;Kennedy J;King N;Korszun A;Knight J;Owen M;Parikh S;Strauss J;Sterne A;Tozzi F;Perry J;Muglia P;Vincent J;McGuffin P;Farmer A
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第7期
77.Limited genetic covariance between autistic traits and intelligence: Findings from a longitudinal twin study

机译：自闭症特征与智力之间有限的遗传协方差：来自一项纵向双胞胎研究的发现
- 作者：HoekstraR.A.;HappéF.;Baron-CohenS.;RonaldA.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第5期
- Autism;
- Childhood;
- Genetics;
- Intellectual disability;
- Twins;
78.The DRD3 rs6280 polymorphism and prevalence of tardive dyskinesia: A meta-analysis

机译：DRD3 rs6280基因多态性与迟发性运动障碍患病率的荟萃分析
- 作者：TsaiH.-T.;NorthK.E.;WestS.L.;PooleC.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Dopamine receptor 3;
- Meta-analysis;
- rs6280;
- Tardive dyskinesia;
79.A systematic association mapping on chromosome 6q in bipolar affective disorder - Evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorder

机译：双相情感障碍中6q染色体上的系统关联映射-黑色素浓缩激素受体2基因作为双相情感障碍危险因素的证据
- 作者：JamraR.A.;SchulzeT.G.;BeckerT.;BrockschmidtF.F.;GreenE.;AlblasM.A.;WendlandJ.R.;AdliM.;GrozevaD.;StrohmeierJ.;GeorgiA.;CraddockN.;ProppingP.;RietschelM.;N?thenM.M.;CichonS.;SchumacherJ.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第4期
- BPAD;
- Genotype-phenotype analysis;
- GPR145;
- LD;
- MCHR2;
80.CAG-repeat length and the age of onset in Huntington Disease (HD): A review and validation study of statistical approaches

机译：亨廷顿病（HD）中CAG重复的长度和发病年龄：统计方法的回顾和验证研究
- 作者：LangbehnD.R.;HaydenM.R.;PaulsenJ.S.;JohnsonH.;AylwardE.;BiglanK.;KieburtzK.;OakesD.;ShoulsonI.;GuttmanM.;LandwehrmeyerB.G.;NanceM.;RossC.;StoutJ.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Huntington disease;
- Polyglutamine expansion;
- Prognosis;
- Survival analysis;
81.Childhood maltreatment, the corticotropin-releasing hormone receptor gene and adult depression in the general population.

机译：普通人群中的儿童期虐待，促肾上腺皮质激素释放激素受体基因和成人抑郁症。
- 作者：Grabe HJ;Schwahn C;Appel K;Mahler J;Schulz A;Spitzer C;Fenske K;Barnow S;Lucht M;Freyberger HJ;John U;Teumer A;Wallaschofski H;Nauck M;Volzke H
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第8期
82.No major role for X-inactivation in variations of intelligence and behavioral problems at middle childhood.

机译：在儿童期中期，X失活在智力和行为问题的变化中没有主要作用。
- 作者：Peerbooms OL;Wichers M;Jacobs N;Kenis G;Derom C;Vlietinck R;Thiery E;van Os J;Rutten BP
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第7期
83.Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level

机译：催产素受体基因（OXTR）遗传变异参与高水平自闭症病因的证据
- 作者：WermterA.-K.;Kamp-BeckerI.;HesseP.;Schulte-K?rneG.;StrauchK.;RemschmidtH.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
84.A screen of SLC1A1 for OCD-related alleles

机译：与OCD相关的等位基因的SLC1A1屏幕
- 作者：WangY.;AdamczykA.;ShugartY.Y.;SamuelsJ.F.;GradosM.A.;GreenbergB.D.;KnowlesJ.A.;McCrackenJ.T.;RauchS.L.;MurphyD.L.;RasmussenS.A.;CullenB.;PintoA.;FyerA.J.;PiacentiniJ.;PaulsD.L.;BienvenuO.J.;RiddleM.;LiangK.Y.;ValleD.;WangT.;NestadtG.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- OCD;
- Polymorphism;
- SLC1A1;
85.Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder.

机译：血清素转运蛋白基因的罕见基因型组合与严重人格障碍的治疗反应相关。
- 作者：Perroud N;Salzmann A;Saiz PA;Baca Garcia E;Sarchiapone M;Garcia Portilla MP;Carli V;Vaquero Lorenzo C;Jaussent I;Mouthon D;Vessaz M;Huguelet P;Courtet P;Malafosse A
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第8期
86.Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample

机译：5HTTLPR和压力在抑郁和自杀倾向中相互作用吗？大样本的项目响应分析
- 作者：CoventryW.L.;JamesM.R.;EavesL.J.;GordonS.D.;GillespieN.A.;RyanL.;HeathA.C.;MontgomeryG.W.;MartinN.G.;WrayN.R.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第3期
- Item response theory;
- Life events;
- rs25531;
- Serotonin transporter;
- Suicidality;
87.Sex-specific association of the reelin gene with bipolar disorder

机译：reelin基因与双相情感障碍的性别特异性关联
- 作者：GoesF.S.;WillourV.L.;ZandiP.P.;BelmonteP.L.;MacKinnonD.F.;MondimoreF.M.;SchweizerB.;DePauloJr.J.R.;GershonE.S.;McMahonF.J.;PotashJ.B.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Bipolar disorder;
- Genetics;
- Neurodevelopment;
- Overlap;
- Schizophrenia;
88.The association of the dopamine transporter gene and the dopamine receptor 2 gene with delirium, a meta-analysis

机译：多巴胺转运蛋白基因和多巴胺受体2基因与del妄的关联，一项荟萃分析
- 作者：VanMunsterB.C.;DeRooijS.E.J.A.;YazdanpanahM.;TienariP.J.;Pitk?l?K.H.;OsseR.J.;AdamisD.;SmitO.;VanDerSteenM.S.;VanHoutenM.;RahkonenT.;SulkavaR.;LaurilaJ.V.;StrandbergT.E.;TulenJ.H.M.;ZwangL.;MacDonaldA.J.D.;TreloarA.;SijbrandsE.J.G.;ZwindermanA.H.;KorevaarJ.C.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Confusion;
- Dopamine;
- Dopamine receptor 2 gene;
- Dopamine transporter gene;
- Elderly;
- Genetics;
89.Association of MεT with social and communication phenotypes in individuals with autism spectrum disorder

机译：自闭症谱系障碍患者中MεT与社交和沟通表型的关联
- 作者：CampbellD.B.;WarrenD.;SutcliffeJ.S.;LeeE.B.;LevittP.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Gastrointestinal;
- Hepatocyte growth factor;
- HGF;
- SRS;
90.GABRR1 and GABRR2, encoding the GABA-A receptor subunits ρ1 and ρ2, are associated with alcohol dependence

机译：编码GABA-A受体亚基ρ1和ρ2的GABRR1和GABRR2与酒精依赖相关
- 作者：XueiX.;Flury-WetherillL.;DickD.;GoateA.;TischfieldJ.;NurnbergerJr.J.;SchuckitM.;KramerJ.;KupermanS.;HesselbrockV.;PorjeszB.;ForoudT.;EdenbergH.J.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Alcoholism;
- GABA-A receptor;
- Genetics;
- Rho subunit;
- Single nucleotide polymorphism;
91.Older paternal age strongly increases the morbidity for schizophrenia in sisters of affected females.

机译：父辈年龄较大会大大增加患病女性姐妹中精神分裂症的发病率。
- 作者：Perrin M;Harlap S;Kleinhaus K;Lichtenberg P;Manor O;Draiman B;Fennig S;Malaspina D
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第7期
92.Analysis of whole genome biomarker expression in blood and brain

机译：血液和大脑中全基因组生物标志物表达的分析
- 作者：RollinsB.;MartinM.V.;MorganL.;VawterM.P.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第4期
- Biomarker;
- Gene expression;
- Whole genome;
93.ADH1A variation predisposes to personality traits and substance dependence

机译：ADH1A变异易导致人格特质和物质依赖
- 作者：ZuoL.;GelernterJ.;KranzlerH.R.;SteinM.B.;ZhangH.;WeiF.;SenS.;PolingJ.;LuoX.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- ADH1A;
- Personality;
- Substance dependence;
94.Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification.

机译：鉴定8p21.1-q11.23染色体上新的遗传基因位点，用于特发性基底节钙化。
- 作者：Dai X;Gao Y;Xu Z;Cui X;Liu J;Li Y;Xu H;Liu M;Wang QK;Liu JY
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第7期
95.FKBP5 polymorphisms and antidepressant response in geriatric depression

机译：FKBP5基因多态性与老年抑郁症的抗抑郁反应
- 作者：SarginsonJ.E.;LazzeroniL.C.;RyanH.S.;SchatzbergA.F.;MurphyJr.G.M.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第2期
- Aged;
- Antidepressive agents;
- FK506 binding protein 5;
- Pharmacogenetics;
96.Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic alzheimer's disease

机译：散发性阿尔茨海默氏病中人类caveolin 1基因上游嘌呤复合体的新型极端纯合子单倍型
- 作者：YeganehM.Z.;MirabzadehA.;KhorshidH.R.K.;KamaliK.;HeshmatiY.;GozalpourE.;VeissyK.;NabiM.O.;NajmabadiH.;OhadiM.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Alzheimer's disease;
- Caveolin 1;
- Haplotype;
- Polymorphism;
- Upstream;
97.ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype

机译：多动症和DAT1：父本风险等位基因和单倍型过度传播的进一步证据
- 作者：HawiZ.;KentL.;HillM.;AnneyR.J.L.;BrookesK.J.;BarryE.;FrankeB.;BanaschewskiT.;BuitelaarJ.;EbsteinR.;MirandaA.;OadesR.D.;RoeyersH.;RothenbergerA.;SergeantJ.;Sonuga-BarkeE.;SteinhausenH.-C.;FaraoneS.V.;AshersonP.;GillM.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- ADHD;
- DAT1;
- Parent of origin effect;
- VNTR;
98.Stathmin, a gene regulating neural plasticity, affects fear and anxiety processing in humans

机译：Stathmin是调节神经可塑性的基因，可影响人类的恐惧和焦虑情绪
- 作者：BrockeB.;LeschK.-P.;ArmbrusterD.;MoserD.A.;MüllerA.;StrobelA.;KirschbaumC.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第1期
- Acoustic startle response;
- Amygdala;
- Anxiety;
- Cortisol response;
- Stathmin;
99.A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder

机译：染色体15q11.2的共分离微复制指出了自闭症谱系障碍的两个风险基因
- 作者：VanDerZwaagB.;StaalW.G.;HochstenbachR.;PootM.;SpierenburgH.A.;DeJongeM.V.;VerbeekN.E.;VantSlotR.;VanEsM.A.;StaalF.J.;FreitagC.M.;Buizer-VoskampJ.E.;NelenM.R.;VanDenBergL.H.;PloosVanAmstelH.K.;VanEngelandH.;BurbachJ.P.H.
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第4期
- Autism spectrum disorder;
- Copy-number;
- Gene expression;
- Gene-dosage;
- Genetics;
100.Coming to grips with complex disorders: Genetic risk prediction in bipolar disorder using panels of genes identified through convergent functional genomics

机译：应对复杂疾病：使用通过融合功能基因组学鉴定的基因组预测躁郁症的遗传风险
- 期刊名称：《American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics》 | 2010年第4期
- Bipolar disorder;
- Convergent functional genomics;
- Epistasis;
- Genetic risk;
- Pathways;
- Prediction;

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