Detalhe da pesquisa
1.
Machine learning approaches to explore digenic inheritance.
Trends Genet
; 38(10): 1013-1018, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35581032
2.
Implication of Melanocortin Receptor Genes in the Familial Comorbidity of Type 2 Diabetes and Depression.
Int J Mol Sci
; 23(15)2022 Jul 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35955479
3.
Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and Depression.
Int J Mol Sci
; 23(17)2022 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36077219
4.
Shared genomic segment analysis with equivalence testing.
Genet Epidemiol
; 44(7): 741-747, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32677112
5.
Population genetics: past, present, and future.
Hum Genet
; 140(2): 231-240, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32683493
6.
Genetic linkage analysis in the age of whole-genome sequencing.
Nat Rev Genet
; 16(5): 275-84, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25824869
7.
Polymorphisms in Stress-Related Genes Are Associated with Reduced Cocaine Abuse and Longer Retention in Methadone Maintenance Treatment for Opioid Use Disorder.
Eur Addict Res
; 27(3): 198-205, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242852
8.
A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS).
Genet Epidemiol
; 43(3): 342-351, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30597647
9.
Variants of opioid genes and response to treatment of opioid use disorder with buprenorphine-naloxone versus extended-release naltrexone in Caucasians.
Am J Drug Alcohol Abuse
; 46(6): 761-768, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32851876
10.
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
Z Kinder Jugendpsychiatr Psychother
; 48(6): 478-489, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33172359
11.
Heterozygosity mapping for human dominant trait variants.
Hum Mutat
; 40(7): 996-1004, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31018026
12.
Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Nature
; 504(7480): 432-6, 2013 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24213632
13.
HDR-del: A tool based on Hamming distance for prioritizing pathogenic chromosomal deletions in exome sequencing.
Hum Mutat
; 38(12): 1796-1800, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28722338
14.
Family-based designs for genome-wide association studies.
Nat Rev Genet
; 12(7): 465-74, 2011 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21629274
15.
HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families.
J Hum Genet
; 61(11): 959-963, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27357426
16.
Polygenic Models for Risk Prediction in Human Genetics.
Hum Hered
; 80(4): 162-4, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27576755
17.
Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis.
Gut
; 64(4): 571-9, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24837172
18.
Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism.
Ann Hum Genet
; 79(5): 329-340, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26094621
19.
Leveling the Playing Field in Homozygosity Mapping Using Map Distances.
Ann Hum Genet
; 79(5): 366-372, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26179257
20.
Overlapping dopaminergic pathway genetic susceptibility to heroin and cocaine addictions in African Americans.
Ann Hum Genet
; 79(3): 188-98, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25875614