متابعة
Martin O. Pollard
Martin O. Pollard
Wellcome Sanger Institute
بريد إلكتروني تم التحقق منه على sanger.ac.uk
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
Twelve years of SAMtools and BCFtools
P Danecek, JK Bonfield, J Liddle, J Marshall, V Ohan, MO Pollard, ...
Gigascience 10 (2), giab008, 2021
50702021
Prevalence and architecture of de novo mutations in developmental disorders
DDD Study
Nature 542 (7642), 433-438, 2017
9242017
The African Genome Variation Project shapes medical genetics in Africa
D Gurdasani, T Carstensen, F Tekola-Ayele, L Pagani, I Tachmazidou, ...
Nature 517 (7534), 327-332, 2015
6172015
Twelve years of SAMtools and BCFtools. Gigascience 10: giab008
P Danecek, JK Bonfield, J Liddle, J Marshall, V Ohan, MO Pollard, ...
4302021
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
A Sifrim, MP Hitz, A Wilsdon, J Breckpot, SH Al Turki, B Thienpont, ...
Nature Genetics 48, 1060–1065, 2016
4042016
Long Reads: their Purpose and Place
MO Pollard, D Gurdasani, AJ Mentzer, T Porter, MS Sandhu
Human molecular genetics, 2018
3612018
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7
Y Luo, KM de Lange, L Jostins, L Moutsianas, J Randall, NA Kennedy, ...
Nature Genetics 49, 186, 2017
2052017
Uganda genome resource enables insights into population history and genomic discovery in Africa
D Gurdasani, T Carstensen, S Fatumo, G Chen, CS Franklin, ...
Cell 179 (4), 984-1002. e36, 2019
1632019
Deep Roots for Aboriginal Australian Y Chromosomes
A Bergström, N Nagle, Y Chen, S McCarthy, MO Pollard, Q Ayub, S Wilcox, ...
Current Biology 26 (6), 809-813, 2016
812016
Very low depth whole genome sequencing in complex trait association studies
A Gilly, K Kuchenbaecker, L Southam, D Suveges, R Moore, G Melloni, ...
bioRxiv, 169789, 2017
762017
INTERVAL Study; UK10K Consortium; Deciphering Developmental Disorders Study. Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified …
A Sifrim, MP Hitz, A Wilsdon, J Breckpot, SH Turki, B Thienpont, J McRae, ...
Nat Genet 48 (9), 1060-5, 2016
402016
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
A Gilly, D Suveges, K Kuchenbaecker, MO Pollard, L Southam, ...
bioRxiv, 283481, 2018
312018
Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot
N Sallah, T Carstensen, K Wakeham, R Bagni, N Labo, MO Pollard, ...
Global Health, Epidemiology and Genomics 2, 2017
122017
Twelve years of samtools and BCFtools. GigaScience, 10 (2)
P Danecek, JK Bonfield, J Liddle, J Marshall, V Ohan, MO Pollard, ...
22021
High-resolution African HLA resource uncoversHLA-DRB1expression effects underlying vaccine response (preprint)
A Mentzer, A Dilthey, M Pollard, D Gurdasani, E Karakoc, T Carstensen, ...
2022
Novel Genome-Wide Sequence Variants Influence Antibody Response to Epstein-Barr Virus in an African Population
N Sallah, T Carstensen, K Wakeham, R Bagni, N Labo, MO Pollard, ...
GENETIC EPIDEMIOLOGY 40 (7), 618-618, 2016
2016
HLA variant identification techniques in African Populations
MO Pollard, S Peacock, N Park, C Pomilla, M Quail, D Gurdasani, ...
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مقالات 1–17