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Genome, Human
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2021
Chia R
,
Sabir MS
,
Bandres-Ciga S
,
Saez-Atienzar S
,
Reynolds RH
,
Gustavsson E
,
Walton RL
,
Ahmed S
,
Viollet C
,
Ding J
et al.
. 2021.
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.
.
Nat Genet. 53(3):294-303.
PubMed
He Z
,
Liu L
,
Wang C
,
Le Guen Y
,
Lee J
,
Gogarten S
,
Lu F
,
Montgomery S
,
Tang H
,
Silverman EK
et al.
. 2021.
Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.
.
Nat Commun. 12(1):3152.
PubMed
2019
Ullah E
,
Mall R
,
Abbas MM
,
Kunji K
,
Nato AQ
,
Bensmail H
,
Wijsman EM
,
Saad M
. 2019.
Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees.
.
Genome Res. 29(1):125-134.
PubMed
Huan T
,
Joehanes R
,
Song C
,
Peng F
,
Guo Y
,
Mendelson M
,
Yao C
,
Liu C
,
Ma J
,
Richard M
et al.
. 2019.
Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.
.
Nat Commun. 10(1):4267.
PubMed
Ebbert MTW
,
Jensen TD
,
Jansen-West K
,
Sens JP
,
Reddy JS
,
Ridge PG
,
Kauwe JSK
,
Belzil V
,
Pregent L
,
Carrasquillo MM
et al.
. 2019.
Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight.
.
Genome Biol. 20(1):97.
PubMed
2018
Amlie-Wolf A
,
Tang M
,
Mlynarski EE
,
Kuksa PP
,
Valladares O
,
Katanić Ž
,
Tsuang D
,
Brown CD
,
Schellenberg GD
,
San Wang L-
. 2018.
INFERNO: inferring the molecular mechanisms of noncoding genetic variants.
.
Nucleic Acids Res. 46(17):8740-8753.
PubMed
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