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Mark Daly

Showing results (91-100 of 149) with videos related to

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American Journal of Human Genetics|April 22, 2008
Consistently replicating locus linked to migraine on 10q22-q23Verneri Anttila, Dale R Nyholt, Mikko Kallela, et al.
Plos One|April 19, 2016
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNAJesper Buchhave Poulsen, Francesco Lescai, Jakob Grove, et al.
Research Square|July 23, 2024
Autoimmune hypothyroidism GWAS reveals independent autoimmune and thyroid-specific contributions and an inverse relation with cancer riskMary Reeve, Masahiro Kanai, Daniel Graham, et al.
Nature Communications|March 20, 2024
SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme diseaseSatu Strausz, Erik Abner, Grace Blacker, et al.
Nature Genetics|April 28, 2006
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosusRobert R Graham, Sergey V Kozyrev, Emily C Baechler, et al.
Nature Communications|March 29, 2025
Assessing the potential causal effects of 1099 plasma metabolites on 2099 binary disease endpointsXianyong Yin, Jack Li, Debraj Bose, et al.
Gastroenterology|July 21, 2015
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel diseaseJudith R Kelsen, Noor Dawany, Christopher J Moran, et al.
American Journal of Human Genetics|December 3, 2014
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseasesAlexander Gusev, S Hong Lee, Gosia Trynka, et al.
Briefings in Bioinformatics|March 27, 2026
Comparison of variant callers using 60 532 multi-ancestry whole genome sequencesHufeng Zhou, Zilin Li, Derek Shyr, et al.
BMJ Open|April 12, 2023
Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disordersMarkku Lähteenvuo, Ari Ahola-Olli, Kimmo Suokas, et al.
Pageof 15

Showing results (91-100 of 149) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|April 22, 2008
Consistently replicating locus linked to migraine on 10q22-q23Verneri Anttila, Dale R Nyholt, Mikko Kallela, et al.
Plos One|April 19, 2016
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNAJesper Buchhave Poulsen, Francesco Lescai, Jakob Grove, et al.
Research Square|July 23, 2024
Autoimmune hypothyroidism GWAS reveals independent autoimmune and thyroid-specific contributions and an inverse relation with cancer riskMary Reeve, Masahiro Kanai, Daniel Graham, et al.
Nature Communications|March 20, 2024
SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme diseaseSatu Strausz, Erik Abner, Grace Blacker, et al.
Nature Genetics|April 28, 2006
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosusRobert R Graham, Sergey V Kozyrev, Emily C Baechler, et al.
Nature Communications|March 29, 2025
Assessing the potential causal effects of 1099 plasma metabolites on 2099 binary disease endpointsXianyong Yin, Jack Li, Debraj Bose, et al.
Gastroenterology|July 21, 2015
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel diseaseJudith R Kelsen, Noor Dawany, Christopher J Moran, et al.
American Journal of Human Genetics|December 3, 2014
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseasesAlexander Gusev, S Hong Lee, Gosia Trynka, et al.
Briefings in Bioinformatics|March 27, 2026
Comparison of variant callers using 60 532 multi-ancestry whole genome sequencesHufeng Zhou, Zilin Li, Derek Shyr, et al.
BMJ Open|April 12, 2023
Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disordersMarkku Lähteenvuo, Ari Ahola-Olli, Kimmo Suokas, et al.
Pageof 15