Works matching IS 15524841 AND DT 2015 AND VI 168B AND IP 7

Results: 13

Oxytocin system social function impacts in children with attention-deficit/hyperactivity disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 609, doi. 10.1002/ajmg.b.32343

By:

Ayaz, Ayşe Burcu;
Karkucak, Mutlu;
Ayaz, Muhammed;
Gokce, Sebla;
Kayan, Esengul;
Güler, Elif Erol;
Güngen, Belma Doğan;
Kuşcu, Tugba Didem;
Ocakoğlu, Gökhan;
Yakut, Tahsin

Publication type:

Article

Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 617, doi. 10.1002/ajmg.b.32344

By:

Fullerton, Janice M.;
Koller, Daniel L.;
Edenberg, Howard J.;
Foroud, Tatiana;
Liu, Hai;
Glowinski, Anne L.;
McInnis, Melvin G.;
Wilcox, Holly C.;
Frankland, Andrew;
Roberts, Gloria;
Schofield, Peter R.;
Mitchell, Philip B.;
Nurnberger, John I.

Publication type:

Article

Associations of common copy number variants in glutathione S-transferase mu 1 and D-dopachrome tautomerase-like protein genes with risk of schizophrenia in a Japanese population.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 630, doi. 10.1002/ajmg.b.32347

By:

Nakamura, Toru;
Ohnuma, Tohru;
Hanzawa, Ryo;
Takebayashi, Yuto;
Takeda, Mayu;
Nishimon, Shohei;
Sannohe, Takahiro;
Katsuta, Narimasa;
Higashiyama, Ryoko;
Shibata, Nobuto;
Arai, Heii

Publication type:

Article

A genome-wide association study of suicidal behavior.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 557, doi. 10.1002/ajmg.b.32330

By:

Galfalvy, Hanga;
Haghighi, Fatemeh;
Hodgkinson, Colin;
Goldman, David;
Oquendo, Maria A.;
Burke, Ainsley;
Huang, Yung‐yu;
Giegling, Ina;
Rujescu, Dan;
Bureau, Alexandre;
Turecki, Gustavo;
Mann, J. John

Publication type:

Article

Quantifying naturalistic social gaze in fragile X syndrome using a novel eye tracking paradigm.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 564, doi. 10.1002/ajmg.b.32331

By:

Hall, Scott S.;
Frank, Michael C.;
Pusiol, Guido T.;
Farzin, Faraz;
Lightbody, Amy A.;
Reiss, Allan L.

Publication type:

Article

Junctophilin 3 ( JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 573, doi. 10.1002/ajmg.b.32332

By:

Krause, Amanda;
Mitchell, Claire;
Essop, Fahmida;
Tager, Susan;
Temlett, James;
Stevanin, Giovanni;
Ross, Christopher;
Rudnicki, Dobrila;
Margolis, Russell

Publication type:

Article

Gene set analysis: A step-by-step guide.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 517, doi. 10.1002/ajmg.b.32328

By:

Mooney, Michael A.;
Wilmot, Beth

Publication type:

Article

Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 595, doi. 10.1002/ajmg.b.32337

By:

Cen, Zhi‐dong;
Xie, Fei;
Lou, Dan‐ning;
Lu, Xing‐jiao;
Ouyang, Zhi‐yuan;
Liu, Ling;
Cao, Jin;
Li, Dan;
Yin, Hou‐min;
Wang, Zhong‐jin;
Xiao, Jian‐feng;
Luo, Wei

Publication type:

Article

Comorbidity of intellectual disability confounds ascertainment of autism: implications for genetic diagnosis.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 600, doi. 10.1002/ajmg.b.32338

By:

Polyak, Andrew;
Kubina, Richard M.;
Girirajan, Santhosh

Publication type:

Article

Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 528, doi. 10.1002/ajmg.b.32324

By:

González‐Peñas, Javier;
Arrojo, Manuel;
Paz, Eduardo;
Brenlla, Julio;
Páramo, Mario;
Costas, Javier

Publication type:

Article

The role of candidate-gene CNTNAP2 in childhood apraxia of speech and specific language impairment.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 536, doi. 10.1002/ajmg.b.32325

By:

Centanni, T. M.;
Sanmann, J. N.;
Green, J. R.;
Iuzzini‐Seigel, J.;
Bartlett, C.;
Sanger, W. G.;
Hogan, T. P.

Publication type:

Article

Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 586, doi. 10.1002/ajmg.b.32336

By:

Nicolas, Gaël;
Charbonnier, Camille;
de Lemos, Roberta Rodrigues;
Richard, Anne‐Claire;
Guillin, Olivier;
Wallon, David;
Legati, Andrea;
Geschwind, Daniel;
Coppola, Giovanni;
Frebourg, Thierry;
Campion, Dominique;
de Oliveira, João Ricardo Mendes;
Hannequin, Didier

Publication type:

Article

Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 544, doi. 10.1002/ajmg.b.32329

By:

Zuo, Lingjun;
Saba, Laura;
Lin, Xiandong;
Tan, Yunlong;
Wang, Kesheng;
Krystal, John H.;
Tabakoff, Boris;
Luo, Xingguang

Publication type:

Article