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Kidney International
|
October 20, 2024
Corrigendum to "Acute kidney injury genetic risks: taking it 1 SNP at a time." Kidney International 2024;106:188-190
Ian B Stanaway, Pavan K Bhatraju, Jonathan Himmelfarb
Kidney International
|
July 20, 2024
Acute kidney injury genetic risks: taking it 1 SNP at a time
Jonathan Himmelfarb, Ian B Stanaway, Pavan K Bhatraju
Drug Metabolism Reviews
|
May 9, 2008
The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies
Mark J Rieder, Robert J Livingston, Ian B Stanaway, et al.
Human Molecular Genetics
|
April 29, 2006
Direct detection of null alleles in SNP genotyping data
Christopher S Carlson, Joshua D Smith, Ian B Stanaway, et al.
Nature Communications
|
March 3, 2025
Author Correction: Multi-ancestry meta-analysis of genome-wide association studies discovers 67 new loci associated with chronic back pain
Ian B Stanaway, Pradeep Suri, Niloofar Afari, et al.
Pain Medicine (Malden, Mass.)
|
November 26, 2024
A Mendelian randomization study finds no evidence for causal effects of C-reactive protein on chronic pain conditions
Pradeep Suri, Yakov A Tsepilov, Elizaveta E Elgaeva, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 15, 2024
No evidence for causal effects of C-reactive protein (CRP) on chronic pain conditions: a Mendelian randomization study
Pradeep Suri, Yakov A Tsepilov, Elizaveta E Elgaeva, et al.
Nature Communications
|
February 11, 2025
Multi-ancestry meta-analysis of genome-wide association studies discovers 67 new loci associated with chronic back pain
Ian B Stanaway, Pradeep Suri, Niloofar Afari, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
August 1, 2009
Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome
Carrie L Heike, Jacqueline R Starr, Mark J Rieder, et al.
American Journal of Medical Genetics. Part A
|
January 5, 2011
IGF1R variants associated with isolated single suture craniosynostosis
Michael L Cunningham, Jeremy A Horst, Mark J Rieder, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 75) with videos related to
Sort By:
Page
of 8
Kidney International
|
October 20, 2024
Corrigendum to "Acute kidney injury genetic risks: taking it 1 SNP at a time." Kidney International 2024;106:188-190
Ian B Stanaway, Pavan K Bhatraju, Jonathan Himmelfarb
Kidney International
|
July 20, 2024
Acute kidney injury genetic risks: taking it 1 SNP at a time
Jonathan Himmelfarb, Ian B Stanaway, Pavan K Bhatraju
Drug Metabolism Reviews
|
May 9, 2008
The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies
Mark J Rieder, Robert J Livingston, Ian B Stanaway, et al.
Human Molecular Genetics
|
April 29, 2006
Direct detection of null alleles in SNP genotyping data
Christopher S Carlson, Joshua D Smith, Ian B Stanaway, et al.
Nature Communications
|
March 3, 2025
Author Correction: Multi-ancestry meta-analysis of genome-wide association studies discovers 67 new loci associated with chronic back pain
Ian B Stanaway, Pradeep Suri, Niloofar Afari, et al.
Pain Medicine (Malden, Mass.)
|
November 26, 2024
A Mendelian randomization study finds no evidence for causal effects of C-reactive protein on chronic pain conditions
Pradeep Suri, Yakov A Tsepilov, Elizaveta E Elgaeva, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 15, 2024
No evidence for causal effects of C-reactive protein (CRP) on chronic pain conditions: a Mendelian randomization study
Pradeep Suri, Yakov A Tsepilov, Elizaveta E Elgaeva, et al.
Nature Communications
|
February 11, 2025
Multi-ancestry meta-analysis of genome-wide association studies discovers 67 new loci associated with chronic back pain
Ian B Stanaway, Pradeep Suri, Niloofar Afari, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
August 1, 2009
Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome
Carrie L Heike, Jacqueline R Starr, Mark J Rieder, et al.
American Journal of Medical Genetics. Part A
|
January 5, 2011
IGF1R variants associated with isolated single suture craniosynostosis
Michael L Cunningham, Jeremy A Horst, Mark J Rieder, et al.
Page
of 8