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Hilary C. Martin
Observed names:
Hilary C Martin,
Hilary Martin,
Hilary C. Martin,
Martin, H.C.
Institution:
Wellcome Sanger Institute
Observed institutions:
Centre for Human Genetics,
The University of Queensland,
Wellcome Sanger Institute,
University of Oxford,
Institute for Molecular Bioscience,
Newcastle University
show all 6
OpenAlex ID:
A5113695742
Genome-wide association studies
2021
·
Emil Uffelmann
, Qin Qin Huang
, et al.
·
Nature Reviews Methods Primers
·
1,796
PDF
Mapping the human genetic architecture of COVID-19
2021
·
COVID-19 Host Genetics Initiative
, COVID-19 Host Genetics InitiativeLeadership
, et al.
·
Nature
·
983
The power of genetic diversity in genome-wide association studies of lipids
2021
·
Sarah E. Graham
, Shoa L. Clarke
, et al.
·
Nature
·
967
PDF
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
2020
·
Ming-Huei Chen
, Laura M. Raffield
, et al.
·
Cell
·
658
PDF
Evidence for 28 genetic disorders discovered by combining healthcare and research data
2020
·
Joanna Kaplanis
, Kaitlin E. Samocha
, et al.
·
Nature
·
609
PDF
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
2022
·
Wei Zhou
, Masahiro Kanai
, et al.
·
Cell Genomics
·
432
PDF
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
2015
·
Jenny C Taylor
, Hilary C Martin
, et al.
·
Nature Genetics
·
376
MicroRNAs and their isomiRs function cooperatively to target common biological pathways
2011
·
Nicole Cloonan
, Shivangi Wani
, et al.
·
Genome biology
·
344
PDF
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
2018
·
Mari E. K. Niemi
, Hilary C. Martin
, et al.
·
Nature
·
339
PDF
Whole-genome sequencing reveals host factors underlying critical COVID-19
2022
·
Athanasios Kousathanas
, Erola Pairo-Castineira
, et al.
·
Nature
·
326
PDF
Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies
2025
·
Mark J. Adams
, Fabian Streit
, et al.
·
Cell
·
280
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
2016
·
Jun Li
, Susan L. Woods
, et al.
·
The American Journal of Human Genetics
·
270
PDF
Recommendations for clinical interpretation of variants found in non-coding regions of the genome
2022
·
Jamie M. Ellingford
, Joo Wook Ahn
, et al.
·
Genome Medicine
·
259
PDF
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
2014
·
H. C. Martin
, G. E. Kim
, et al.
·
Human Molecular Genetics
·
258
PDF
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland
2023
·
Caroline F. Wright
, Patrick Campbell
, et al.
·
New England Journal of Medicine
·
219
PDF
Quantifying the contribution of recessive coding variation to developmental disorders
2018
·
Hilary C. Martin
, Wendy D. Jones
, et al.
·
Science
·
200
PDF
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
2024
·
Xiangrui Meng
, Georgina Navoly
, et al.
·
Nature Genetics
·
187
PDF
Evaluating drug targets through human loss-of-function genetic variation
2020
·
Eric Vallabh Minikel
, Konrad J. Karczewski
, et al.
·
Nature
·
187
PDF
A first update on mapping the human genetic architecture of COVID-19
2022
·
COVID-19 Host Genetics Initiative
, COVID-19 Host Genetics Initiative
, et al.
·
Nature
·
181
PDF
miR-139-5p is a regulator of metastatic pathways in breast cancer
2013
·
Keerthana Krishnan
, Anita L. Steptoe
, et al.
·
RNA
·
176
PDF
Geographical genomics of human leukocyte gene expression variation in southern Morocco
2009
·
Youssef Idaghdour
, Wendy Czika
, et al.
·
Nature Genetics
·
151
PDF
Genetic correlates of phenotypic heterogeneity in autism
2022
·
Varun Warrier
, Xinhe Zhang
, et al.
·
Nature Genetics
·
146
PDF
MC3R links nutritional state to childhood growth and the timing of puberty
2021
·
B. Y. H. Lam
, A. Williamson
, et al.
·
Nature
·
139
Polygenic prediction of preeclampsia and gestational hypertension
2023
·
Michael C. Honigberg
, Buu Truong
, et al.
·
Nature Medicine
·
136
PDF
Imperfect centered miRNA binding sites are common and can mediate repression of target mRNAs
2014
·
Hilary C Martin
, Shivangi Wani
, et al.
·
Genome biology
·
131
PDF
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Works count:
11
Citation count:
1,174
H-index:
6
I10-index:
6
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