Detalhe da pesquisa
1.
Rare genetic variants underlie outlying levels of DNA methylation and gene-expression.
Hum Mol Genet
; 32(11): 1912-1921, 2023 05 18.
Artigo
Inglês
| MEDLINE | ID: mdl-36790133
2.
A locus conferring tolerance to Theileria infection in African cattle.
PLoS Genet
; 18(4): e1010099, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35446841
3.
Investigating the Role of Brain Natriuretic Peptide (BNP) and N-Terminal-proBNP in Thrombosis and Acute Ischemic Stroke Etiology.
Int J Mol Sci
; 25(5)2024 Mar 05.
Artigo
Inglês
| MEDLINE | ID: mdl-38474245
4.
Graphia: A platform for the graph-based visualisation and analysis of high dimensional data.
PLoS Comput Biol
; 18(7): e1010310, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35877685
5.
Mapping restricted introgression across the genomes of admixed indigenous African cattle breeds.
Genet Sel Evol
; 55(1): 91, 2023 Dec 14.
Artigo
Inglês
| MEDLINE | ID: mdl-38097935
6.
Using machine learning to detect the differential usage of novel gene isoforms.
BMC Bioinformatics
; 23(1): 45, 2022 Jan 18.
Artigo
Inglês
| MEDLINE | ID: mdl-35042461
7.
Assessment of genotyping array performance for genome-wide association studies and imputation in African cattle.
Genet Sel Evol
; 54(1): 58, 2022 Sep 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36057548
8.
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.
PLoS Genet
; 15(11): e1008480, 2019 11.
Artigo
Inglês
| MEDLINE | ID: mdl-31765389
9.
Comparison of VÌo2peak and VÌo2max at Different Sampling Intervals in Collegiate Wrestlers.
J Strength Cond Res
; 35(10): 2915-2917, 2021 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34550099
10.
Shared regulatory sites are abundant in the human genome and shed light on genome evolution and disease pleiotropy.
PLoS Genet
; 13(3): e1006673, 2017 03.
Artigo
Inglês
| MEDLINE | ID: mdl-28282383
11.
The host ubiquitin-dependent segregase VCP/p97 is required for the onset of human cytomegalovirus replication.
PLoS Pathog
; 13(5): e1006329, 2017 May.
Artigo
Inglês
| MEDLINE | ID: mdl-28494016
12.
Comparison of Physical Fitness Parameters for Starters vs. Nonstarters in an NCAA Division I Men's Lacrosse Team.
J Strength Cond Res
; 32(11): 3160-3168, 2018 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-30216251
13.
A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma.
Hum Mutat
; 38(8): 942-946, 2017 08.
Artigo
Inglês
| MEDLINE | ID: mdl-28493397
14.
Homozygous loss-of-function variants in European cosmopolitan and isolate populations.
Hum Mol Genet
; 24(19): 5464-74, 2015 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26173456
15.
hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets.
Mol Biol Evol
; 32(11): 3027-9, 2015 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-26248562
16.
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.
Nat Genet
; 39(8): 989-94, 2007 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-17618283
17.
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.
Twin Res Hum Genet
; 18(2): 117-25, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25744449
18.
Abundant pleiotropy in human complex diseases and traits.
Am J Hum Genet
; 89(5): 607-18, 2011 Nov 11.
Artigo
Inglês
| MEDLINE | ID: mdl-22077970
19.
Widespread signatures of recent selection linked to nucleosome positioning in the human lineage.
Genome Res
; 21(11): 1777-87, 2011 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-21903742
20.
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
PLoS Genet
; 7(6): e1002105, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21655089