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Ian B Stanaway

Showing results (1-10 of 75) with videos related to

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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;106:188-190Ian B Stanaway, Pavan K Bhatraju, Jonathan Himmelfarb
Kidney International|July 20, 2024
Acute kidney injury genetic risks: taking it 1 SNP at a timeJonathan 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 studiesMark J Rieder, Robert J Livingston, Ian B Stanaway, et al.
Human Molecular Genetics|April 29, 2006
Direct detection of null alleles in SNP genotyping dataChristopher 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 painIan 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 conditionsPradeep 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 studyPradeep 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 painIan 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 syndromeCarrie 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 craniosynostosisMichael L Cunningham, Jeremy A Horst, Mark J Rieder, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Kidney International|October 20, 2024
Corrigendum to "Acute kidney injury genetic risks: taking it 1 SNP at a time." Kidney International 2024;106:188-190Ian B Stanaway, Pavan K Bhatraju, Jonathan Himmelfarb
Kidney International|July 20, 2024
Acute kidney injury genetic risks: taking it 1 SNP at a timeJonathan 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 studiesMark J Rieder, Robert J Livingston, Ian B Stanaway, et al.
Human Molecular Genetics|April 29, 2006
Direct detection of null alleles in SNP genotyping dataChristopher 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 painIan 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 conditionsPradeep 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 studyPradeep 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 painIan 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 syndromeCarrie 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 craniosynostosisMichael L Cunningham, Jeremy A Horst, Mark J Rieder, et al.
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