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Respiratory Research
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June 9, 2026
Genetic and epidemiological evidence linking respiratory and musculoskeletal diseases: shared risk factors and intervention windows
Olivia Murrin, Bethany Voller, Ruby M Woodward, et al.
Human Genetics
|
April 18, 2003
Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes
Rebecca C J Twells, Charles A Mein, Felicity Payne, et al.
Plos One
|
January 26, 2013
Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs
Vipin Gupta, Donipadi Guru Vinay, Ulla Sovio, et al.
European Journal of Human Genetics : EJHG
|
November 6, 2009
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis
Inger-Lise Mero, Aslaug R Lorentzen, Maria Ban, et al.
BMC Genomics
|
February 26, 2024
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Kharis Burns, Benjamin H Mullin, Loes M E Moolhuijsen, et al.
Heart (British Cardiac Society)
|
July 2, 2016
Marginal role for 53 common genetic variants in cardiovascular disease prediction
Richard W Morris, Jackie A Cooper, Tina Shah, et al.
Nature Communications
|
February 2, 2022
The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples
James E Barrett, Chiara Herzog, Allison Jones, et al.
European Journal of Endocrinology
|
September 15, 2021
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
James Nolan, Purdey J Campbell, Suzanne J Brown, et al.
Nature Reviews. Clinical Oncology
|
February 28, 2018
Epigenome-based cancer risk prediction: rationale, opportunities and challenges
Martin Widschwendter, Allison Jones, Iona Evans, et al.
Neurobiology of Aging
|
February 4, 2012
Alzheimer's disease and age-related macular degeneration have different genetic models for complement gene variation
Petroula Proitsi, Michelle K Lupton, Frank Dudbridge, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 193) with videos related to
Sort By:
Page
of 20
Respiratory Research
|
June 9, 2026
Genetic and epidemiological evidence linking respiratory and musculoskeletal diseases: shared risk factors and intervention windows
Olivia Murrin, Bethany Voller, Ruby M Woodward, et al.
Human Genetics
|
April 18, 2003
Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes
Rebecca C J Twells, Charles A Mein, Felicity Payne, et al.
Plos One
|
January 26, 2013
Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs
Vipin Gupta, Donipadi Guru Vinay, Ulla Sovio, et al.
European Journal of Human Genetics : EJHG
|
November 6, 2009
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis
Inger-Lise Mero, Aslaug R Lorentzen, Maria Ban, et al.
BMC Genomics
|
February 26, 2024
Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Kharis Burns, Benjamin H Mullin, Loes M E Moolhuijsen, et al.
Heart (British Cardiac Society)
|
July 2, 2016
Marginal role for 53 common genetic variants in cardiovascular disease prediction
Richard W Morris, Jackie A Cooper, Tina Shah, et al.
Nature Communications
|
February 2, 2022
The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples
James E Barrett, Chiara Herzog, Allison Jones, et al.
European Journal of Endocrinology
|
September 15, 2021
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
James Nolan, Purdey J Campbell, Suzanne J Brown, et al.
Nature Reviews. Clinical Oncology
|
February 28, 2018
Epigenome-based cancer risk prediction: rationale, opportunities and challenges
Martin Widschwendter, Allison Jones, Iona Evans, et al.
Neurobiology of Aging
|
February 4, 2012
Alzheimer's disease and age-related macular degeneration have different genetic models for complement gene variation
Petroula Proitsi, Michelle K Lupton, Frank Dudbridge, et al.
Page
of 20