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

Results: 12

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
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
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
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
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
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