Detalhe da pesquisa
1.
Rare coding variants in ten genes confer substantial risk for schizophrenia.
Nature
; 604(7906): 509-516, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396579
2.
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
; 604(7906): 502-508, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396580
3.
Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 180(4): 258-265, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30859703
4.
Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia.
Ann Hum Genet
; 82(2): 88-92, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29148569
5.
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 174(7): 724-731, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28719003
6.
Familial Screening for the Prevention of Rare Diseases: A Focus on Lipodystrophy in Southern Saudi Arabia.
J Epidemiol Glob Health
; 14(1): 162-168, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38231342
7.
Reclassifying variations of unknown significance in diseases affecting Saudi Arabia's population reveal new associations.
Front Genet
; 14: 1250317, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38028588
8.
Prospect of genetic disorders in Saudi Arabia.
Front Genet
; 14: 1243518, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37799141
9.
Perceptions of Saudis Toward Participating in the COVID-19 Convalescent Plasma Clinical Trial.
Cureus
; 15(11): e48879, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-38106720
10.
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nat Genet
; 53(6): 817-829, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34002096