Detalhe da pesquisa
1.
The time and place of European admixture in Ashkenazi Jewish history.
PLoS Genet
; 13(4): e1006644, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28376121
2.
Identification of a missense variant in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk for type 2 diabetes in Ashkenazi Jewish individuals.
Diabetologia
; 61(10): 2180-2188, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30014265
3.
High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation.
Hum Genet
; 137(4): 343-355, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29705978
4.
A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.
Gastroenterology
; 151(4): 710-723.e2, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27377463
5.
Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Nat Genet
; 40(9): 1053-5, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18677311
6.
Excess of homozygosity in the major histocompatibility complex in schizophrenia.
Hum Mol Genet
; 23(22): 6088-95, 2014 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24943592
7.
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Hum Mol Genet
; 23(17): 4693-702, 2014 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24842889
8.
Expanded genetic screening panel for the Ashkenazi Jewish population.
Genet Med
; 18(5): 522-8, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26334176
9.
Length distributions of identity by descent reveal fine-scale demographic history.
Am J Hum Genet
; 91(5): 809-22, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103233
10.
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
PLoS Genet
; 8(3): e1002559, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22412388
11.
Genome-wide association study of schizophrenia in Ashkenazi Jews.
Am J Med Genet B Neuropsychiatr Genet
; 168(8): 649-59, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26198764
12.
Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment.
Am J Med Genet B Neuropsychiatr Genet
; 168B(5): 363-73, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25951819
13.
The architecture of long-range haplotypes shared within and across populations.
Mol Biol Evol
; 29(2): 473-86, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21984068
14.
Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2.
Genome Res
; 20(9): 1180-90, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20688780
15.
The Collaborative Cross, a community resource for the genetic analysis of complex traits.
Nat Genet
; 36(11): 1133-7, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15514660
16.
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.
PLoS Genet
; 4(2): e28, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18282107
17.
Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia.
Neuron
; 109(9): 1465-1478.e4, 2021 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33756103
18.
Closing in on complex traits.
Nat Genet
; 38(8): 861-2, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16874323
19.
Correlational analysis for identifying genes whose regulation contributes to chronic neuropathic pain.
Mol Pain
; 5: 7, 2009 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19228393
20.
Association between golli-MBP and schizophrenia in the Jewish Ashkenazi population: are regulatory regions involved?
Int J Neuropsychopharmacol
; 12(7): 885-94, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19154657