Works matching IS 15524841 AND DT 2018 AND VI 177 AND IP 8

Results: 12

Musical auditory processing, cognition, and psychopathology in 22q11.2 deletion syndrome.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 765, doi. 10.1002/ajmg.b.32690

By:

Gao, Lucy;
Tang, Sunny X.;
Yi, James J.;
McDonald‐McGinn, Donna M.;
Zackai, Elaine H.;
Emanuel, Beverly S.;
Gur, Ruben C.;
Calkins, Monica E.;
Gur, Raquel E.

Publication type:

Article

Cover Image, Volume 177B, Number 8, December 2018.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. i, doi. 10.1002/ajmg.b.32703
Publication type:: Article

Genotype–phenotype correlations in Darier disease: A focus on the neuropsychiatric phenotype.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 717, doi. 10.1002/ajmg.b.32679

By:

Gordon‐Smith, Katherine;
Green, Elaine;
Grozeva, Detelina;
Tavadia, Sherine;
Craddock, Nick;
Jones, Lisa

Publication type:

Article

DRD4 methylation as a potential biomarker for physical aggression: An epigenome‐wide, cross‐tissue investigation.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 746, doi. 10.1002/ajmg.b.32689

By:

Cecil, Charlotte A. M.;
Walton, Esther;
Pingault, Jean‐Baptiste;
Provençal, Nadine;
Pappa, Irene;
Vitaro, Frank;
Côté, Sylvana;
Szyf, Moshe;
Tremblay, Richard E.;
Tiemeier, Henning;
Viding, Essi;
McCrory, Eamon J.

Publication type:

Article

PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 736, doi. 10.1002/ajmg.b.32688

By:

Khalil, Raida;
Kenny, Connor;
Hill, R. Sean;
Mochida, Ganeshwaran H.;
Nasir, Ramzi;
Partlow, Jennifer N.;
Barry, Brenda J.;
Al‐Saffar, Muna;
Egan, Chloe;
Stevens, Christine R.;
Gabriel, Stacey B.;
Barkovich, A. James;
Ellison, Jay W.;
Al‐Gazali, Lihadh;
Walsh, Christopher A.;
Chahrour, Maria H.

Publication type:

Article

Association of Alzheimer's genetic loci with mild behavioral impairment.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 727, doi. 10.1002/ajmg.b.32684

By:

Andrews, Shea J.;
Ismail, Zahinoor;
Anstey, Kaarin J.;
Mortby, Moyra

Publication type:

Article

Gene‐level associations in suicide attempter families show overrepresentation of synaptic genes and genes differentially expressed in brain development.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 774, doi. 10.1002/ajmg.b.32694

By:

Sokolowski, Marcus;
Wasserman, Jerzy;
Wasserman, Danuta

Publication type:

Article

Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 687, doi. 10.1002/ajmg.b.32677

By:

Agostini, Annalisa;
Marchetti, Daniela;
Izzi, Claudia;
Cocco, Isabella;
Pinelli, Lorenzo;
Accorsi, Patrizia;
Iascone Maria, Rosaria;
Giordano, Lucio

Publication type:

Article

Blood‐based dynamic genomic signature for obsessive–compulsive disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 709, doi. 10.1002/ajmg.b.32675

By:

Wang, Yuan;
Cheng, Changming;
Zhang, Zongfeng;
Wang, Jianyu;
Wang, Yao;
Li, Xiaoping;
Gao, Rui;
Wang, Zhen;
Fang, Yiru;
Wang, Jijun;
Wang, Min;
Fan, Qing;
Periya, Sanggetha;
Zhang, Haiyin;
Tsuang, Ming T.;
Liew, Choong‐Chin

Publication type:

Article

Characterization of speech and language phenotype in children with NRXN1 deletions.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 700, doi. 10.1002/ajmg.b.32664

By:

Brignell, Amanda;
St John, Miya;
Boys, Amber;
Bruce, Amanda;
Dinale, Carla;
Pigdon, Lauren;
Hildebrand, Michael S.;
Amor, David J.;
Morgan, Angela T.

Publication type:

Article

CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 691, doi. 10.1002/ajmg.b.32648

By:

Kazeminasab, Somayeh;
Taskiran, Ibrahim Ihsan;
Fattahi, Zohreh;
Bazazzadegan, Niloofar;
Hosseini, Masoumeh;
Rahimi, Maryam;
Oladnabi, Morteza;
Haddadi, Mohammad;
Celik, Arzu;
Ropers, Hans‐Hilger;
Najmabadi, Hossein;
Kahrizi, Kimia

Publication type:

Article

Issue Information ‐ TOC.

Published in:: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 685, doi. 10.1002/ajmg.b.32591
Publication type:: Article