Works matching IS 15524841 AND DT 2016 AND VI 171B AND IP 6

Results: 19

FKBP5 genotype interacts with early life trauma to predict heavy drinking in college students.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 879, doi. 10.1002/ajmg.b.32460

By:

Lieberman, Richard;
Armeli, Stephen;
Scott, Denise M.;
Kranzler, Henry R.;
Tennen, Howard;
Covault, Jonathan

Publication type:

Article

Whole-gene sequencing investigation of SAT1 in attempted suicide.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 888, doi. 10.1002/ajmg.b.32462

By:

Monson, Eric T.;
de Klerk, Kelly;
Gaynor, Sophia C.;
Wagner, Alex H.;
Breen, Marie E.;
Parsons, Meredith;
Casavant, Thomas L.;
Zandi, Peter P.;
Potash, James B.;
Willour, Virginia L.

Publication type:

Article

Common variants in CACNA1C and MDD susceptibility: A comprehensive meta-analysis.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 896, doi. 10.1002/ajmg.b.32466

By:

Rao, Shuquan;
Yao, Yao;
Zheng, Chuan;
Ryan, Joanne;
Mao, Canquan;
Zhang, Fuquan;
Meyre, David;
Xu, Qi

Publication type:

Article

Multimarker analysis suggests the involvement of BDNF signaling and microRNA biosynthesis in suicidal behavior.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 763, doi. 10.1002/ajmg.b.32433

By:

Pulay, Attila J.;
Réthelyi, János M.

Publication type:

Article

An examination of the language construct in NIMH's research domain criteria: Time for reconceptualization!

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 904, doi. 10.1002/ajmg.b.32438

By:

Elvevåg, Brita;
Cohen, Alex S.;
Wolters, Maria K.;
Whalley, Heather C.;
Gountouna, Viktoria‐Eleni;
Kuznetsova, Ksenia A.;
Watson, Andrew R.;
Nicodemus, Kristin K.

Publication type:

Article

15q13.3 duplication in two patients with childhood-onset schizophrenia.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 777, doi. 10.1002/ajmg.b.32439

By:

Zhou, Dale;
Gochman, Peter;
Broadnax, Diane D.;
Rapoport, Judith L.;
Ahn, Kwangmi

Publication type:

Article

Transcriptome analysis of genes and gene networks involved in aggressive behavior in mouse and zebrafish.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 827, doi. 10.1002/ajmg.b.32451

By:

Malki, Karim;
Du Rietz, Ebba;
Crusio, Wim E.;
Pain, Oliver;
Paya‐Cano, Jose;
Karadaghi, Rezhaw L.;
Sluyter, Frans;
de Boer, Sietse F.;
Sandnabba, Kenneth;
Schalkwyk, Leonard C.;
Asherson, Philip;
Tosto, Maria Grazia

Publication type:

Article

PARK16 is associated with PD in the Malaysian population.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 839, doi. 10.1002/ajmg.b.32454

By:

Gopalai, Aroma Agape;
Ahmad‐Annuar, Azlina;
Li, Hui‐Hua;
Zhao, Yi;
Lim, Shen‐Yang;
Tan, Ai Huey;
Lim, Thien Thein;
Eow, Gaik Bee;
Santhi, Puvanarajah;
Shanthi, Viswanathan;
Norlinah, Mohamed Ibrahim;
Aziz, Zariah Abdul;
Lim, Soo Kun;
Tan, Chong Tin;
Tan, Eng‐King

Publication type:

Article

The role of protein intrinsic disorder in major psychiatric disorders.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 848, doi. 10.1002/ajmg.b.32455

By:

Tovo‐Rodrigues, Luciana;
Recamonde‐Mendoza, Mariana;
Paixão‐Côrtes, Vanessa Rodrigues;
Bruxel, Estela M.;
Schuch, Jaqueline B.;
Friedrich, Deise C.;
Rohde, Luis A.;
Hutz, Mara H.

Publication type:

Article

The ANK3 gene and facial affect processing: An ERP study.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 861, doi. 10.1002/ajmg.b.32456

By:

Zhao, Wan;
Zhang, Qiumei;
Yu, Ping;
Zhang, Zhifang;
Chen, Xiongying;
Gu, Huang;
Zhai, Jinguo;
Chen, Min;
Du, Boqi;
Deng, Xiaoxiang;
Ji, Feng;
Wang, Chuanyue;
Xiang, Yu‐Tao;
Li, Dawei;
Wu, Hongjie;
Dong, Qi;
Luo, Yuejia;
Li, Jun;
Chen, Chuansheng

Publication type:

Article

Preliminary examination of microRNA expression profiling in bipolar disorder I patients during antipsychotic treatment.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 867, doi. 10.1002/ajmg.b.32457

By:

Lim, Chor Hong;
Zainal, Nor Zuraida;
Kanagasundram, Sharmilla;
Zain, Shamsul Mohd;
Mohamed, Zahurin

Publication type:

Article

Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 875, doi. 10.1002/ajmg.b.32458

By:

Kurth, Ingo;
Baumgartner, Manuela;
Schabhüttl, Maria;
Tomni, Cecilia;
Windhager, Reinhard;
Strom, Tim M.;
Wieland, Thomas;
Gremel, Kurt;
Auer‐Grumbach, Michaela

Publication type:

Article

Cover Image, Volume 171B, Number 6, September 2016.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. i, doi. 10.1002/ajmg.b.32490

By:

Mooney, Michael A.;
McWeeney, Shannon K.;
Faraone, Stephen V.;
Hinney, Anke;
Hebebrand, Johannes;
Nigg, Joel T.;
Wilmot, Beth

Publication type:

Article

Issue Information - TOC.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 761, doi. 10.1002/ajmg.b.32371
Publication type:: Article

COMT genotype is associated with differential expression of muscarinic M1 receptors in human cortex.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 784, doi. 10.1002/ajmg.b.32440

By:

Dean, Brian;
Scarr, Elizabeth

Publication type:

Article

Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 790, doi. 10.1002/ajmg.b.32441

By:

Klaassen, Petra;
Duijff, Sasja;
Swanenburg de Veye, Henriëtte;
Beemer, Frits;
Sinnema, Gerben;
Breetvelt, Elemi;
Schappin, Renske;
Vorstman, Jacob

Publication type:

Article

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 797, doi. 10.1002/ajmg.b.32444

By:

Egawa, Jun;
Hoya, Satoshi;
Watanabe, Yuichiro;
Nunokawa, Ayako;
Shibuya, Masako;
Ikeda, Masashi;
Inoue, Emiko;
Okuda, Shujiro;
Kondo, Kenji;
Saito, Takeo;
Kaneko, Naoshi;
Muratake, Tatsuyuki;
Igeta, Hirofumi;
Iwata, Nakao;
Someya, Toshiyuki

Publication type:

Article

Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 806, doi. 10.1002/ajmg.b.32445

By:

Duarte, Rodrigo R. R.;
Troakes, Claire;
Nolan, Matthew;
Srivastava, Deepak P.;
Murray, Robin M.;
Bray, Nicholas J.

Publication type:

Article

Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 815, doi. 10.1002/ajmg.b.32446

By:

Mooney, Michael A.;
McWeeney, Shannon K.;
Faraone, Stephen V.;
Hinney, Anke;
Hebebrand, Johannes;
Romanos, Marcel;
Warnke, Andreas;
Reif, Andreas;
Walitza, Susanne;
Roeyers, Herbert;
Franke, Barbara;
Buitelaar, Jan K.;
Lesch, Klaus‐Peter;
Kent, Lindsey;
Vasquez, Alejandro Arias;
Thapar, Anita;
Martin, Joanna;
O'Donovan, Michael C.;
Owen, Michael J.;
Williams, Nigel

Publication type:

Article