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Author Details
Full Name
David Sexton
Affiliation
ORCID
Career Start Year
1997
Papers
20
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34971674
CellDepot: A Unified Repository for scRNA-seq Data and Visual Exploration.
Journal of Molecular Biology
2022
37117740
The burden of rare protein-truncating genetic variants on human lifespan.
2022
34741066
Pairwise effects between lipid GWAS genes modulate lipid plasma levels and cellular uptake.
Nat Commun
2021
30586382
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.
PLoS Genet
2018
22584458
Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes.
Pharmacogenomics J
2013
22579044
Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development.
Cell
2012
21833088
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
2011
22216009
Acute multiple organ failure in adult mice deleted for the developmental regulator Wt1.
PLoS Genet
2011
21750680
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.
PLoS Genet
2011
19908384
Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data.
Pac Symp Biocomput
2010
20574445
A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.
Genes Immun
2010
20422016
Consanguinity mapping of congenital heart disease in a South Indian population.
PLoS One
2010
20502484
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
Nat Genet
2010
19557184
The need for centralization of computational biology resources.
PLoS Comput Biol
2009
19557125
Managing and analyzing next-generation sequence data.
PLoS Computational Biology
2009
19293837
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor.
Eur J Hum Genet
2009
15469410
Genetic variation in eleven phase I drug metabolism genes in an ethnically diverse population.
Pharmacogenomics
2004
11957135
A major predisposition locus for severe obesity, at 4p15-p14.
American Journal of Human Genetics
2002
9288787
Localization of SMAD5 and its evaluation as a candidate myeloid tumor suppressor.
Cancer Research
1997
9331070
Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor.
Cancer Res
1997
1 - 20 of 20
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