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Plos One
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December 30, 2022
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes
Waheed Ul-Rahman Ahmed, Manal I A Patel, Michael Ng, et al.
The Journal of Craniofacial Surgery
|
August 28, 2014
Lessons learned in posterior cranial vault distraction
Gregory P L Thomas, Steven A Wall, Jayaratnam Jayamohan, et al.
American Journal of Medical Genetics. Part A
|
March 28, 2013
The fibroblast growth factor receptor 2 p.Ala172Phe mutation in Pfeiffer syndrome--history repeating itself
Sally Jay, Akira Wiberg, Marc Swan, et al.
Brain : a Journal of Neurology
|
September 11, 2019
Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics
Akira Wiberg, Michael Ng, Yasser Al Omran, et al.
Molecular Genetics & Genomic Medicine
|
August 4, 2021
Exome sequencing identifies a disease variant of the mitochondrial ATP-Mg/Pi carrier SLC25A25 in two families with kidney stones
M Reza Jabalameli, Fiona M Fitzpatrick, Roberto Colombo, et al.
Nature Communications
|
June 2, 2022
Genome-wide association analysis and replication in 810,625 individuals with varicose veins
Waheed-Ul-Rahman Ahmed, Sam Kleeman, Michael Ng, et al.
Nature Communications
|
March 6, 2019
A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome
Akira Wiberg, Michael Ng, Annina B Schmid, et al.
BJS Open
|
July 23, 2025
Time to recovery following open and endoscopic carpal tunnel decompression: meta-analysis
Olivia J Hartrick, Rebecca K Turner, Alexander Freethy, et al.
The Lancet. Rheumatology
|
August 31, 2022
Shared genetic susceptibility between trigger finger and carpal tunnel syndrome: a genome-wide association study
Benjamin Patel, Sam O Kleeman, Drew Neavin, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
February 16, 2021
A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity
Yoshifumi Itoh, Michael Ng, Akira Wiberg, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Plos One
|
December 30, 2022
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes
Waheed Ul-Rahman Ahmed, Manal I A Patel, Michael Ng, et al.
The Journal of Craniofacial Surgery
|
August 28, 2014
Lessons learned in posterior cranial vault distraction
Gregory P L Thomas, Steven A Wall, Jayaratnam Jayamohan, et al.
American Journal of Medical Genetics. Part A
|
March 28, 2013
The fibroblast growth factor receptor 2 p.Ala172Phe mutation in Pfeiffer syndrome--history repeating itself
Sally Jay, Akira Wiberg, Marc Swan, et al.
Brain : a Journal of Neurology
|
September 11, 2019
Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics
Akira Wiberg, Michael Ng, Yasser Al Omran, et al.
Molecular Genetics & Genomic Medicine
|
August 4, 2021
Exome sequencing identifies a disease variant of the mitochondrial ATP-Mg/Pi carrier SLC25A25 in two families with kidney stones
M Reza Jabalameli, Fiona M Fitzpatrick, Roberto Colombo, et al.
Nature Communications
|
June 2, 2022
Genome-wide association analysis and replication in 810,625 individuals with varicose veins
Waheed-Ul-Rahman Ahmed, Sam Kleeman, Michael Ng, et al.
Nature Communications
|
March 6, 2019
A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome
Akira Wiberg, Michael Ng, Annina B Schmid, et al.
BJS Open
|
July 23, 2025
Time to recovery following open and endoscopic carpal tunnel decompression: meta-analysis
Olivia J Hartrick, Rebecca K Turner, Alexander Freethy, et al.
The Lancet. Rheumatology
|
August 31, 2022
Shared genetic susceptibility between trigger finger and carpal tunnel syndrome: a genome-wide association study
Benjamin Patel, Sam O Kleeman, Drew Neavin, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
February 16, 2021
A common SNP risk variant MT1-MMP causative for Dupuytren's disease has a specific defect in collagenolytic activity
Yoshifumi Itoh, Michael Ng, Akira Wiberg, et al.
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of 4