Population-scale repeat expansions elucidate disease risk and brain atrophy
Vijay Kumar Pounraja, Jae Hoon Sul, Joseph L. Herman, Sean O’Keeffe et autres
3 citationsNature
Michelle G. LeBlanc
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
68Publications signalées
3014Citations signalées
1Affiliations récentes
Institutions déclarées
Domaines associés
Genetic Associations and EpidemiologyNeonatal Respiratory Health ResearchGenomics and Rare DiseasesTrace Elements in HealthLiver Disease Diagnosis and Treatment
Publications récentes
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries
Veera M. Rajagopal, Andrey Ziyatdinov, Tyler Joseph, Ariane Ayer et autres
0 citationsNature Communications
Genomic Ascertainment of CHEK2 -Related Cancer Predisposition
Sun Young Kim, Jung Kim, Mark Ramos, Jeremy S. Haley et autres
5 citationsJAMA Network Open
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants
Hongbo Liu, Amin Abedini, Eunji Ha, Ziyuan Ma et autres
57 citationsScience
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D. Kessler, Amy Damask, Sean O’Keeffe, Nilanjana Banerjee et autres
0 citationsNature
Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Sun, Xiaodong Bai, Siying Chen, Suying Bao et autres
0 citationsNature
Author response: Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings
Shek Man Chim, Kristen E. Howell, John Dronzek, Weizhen Wu et autres
0 citations
Genetic inactivation of zinc transporter SLC39A5 improves liver function and hyperglycemia in obesogenic settings
Shek Man Chim, Kristen E. Howell, John Dronzek, Weizhen Wu et autres
3 citationseLife
Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk
Oliver Bundgaard Vad, Laia M. Monfort, Christian Paludan‐Müller, Konstantin Kahnert et autres
53 citationsJAMA Cardiology
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Sun, Xiaodong Bai, Siying Chen, Suying Bao et autres
115 citationsNature
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City
Andrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, Joshua Backman et autres
1 citationNature
PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients
Jacqueline Cappadocia, Lisa B. Aiello, Michael J. Kelley, Bryson W. Katona et autres
0 citationsGenetics in Medicine Open
BNTIC News n’est pas le producteur de ces données. Recherche à la demande dans Crossref et Europe PMC, sans clé ; OpenAlex reste optionnel. Aucun service payant requis, aucune réponse conservée. Sources et limites.