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Akira Wiberg

Showing results (21-30 of 37) with videos related to

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Plos One|December 30, 2022
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypesWaheed 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 distractionGregory 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 itselfSally 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 geneticsAkira 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 stonesM 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 veinsWaheed-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 syndromeAkira Wiberg, Michael Ng, Annina B Schmid, et al.
BJS Open|July 23, 2025
Time to recovery following open and endoscopic carpal tunnel decompression: meta-analysisOlivia 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 studyBenjamin 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 activityYoshifumi Itoh, Michael Ng, Akira Wiberg, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Plos One|December 30, 2022
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypesWaheed 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 distractionGregory 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 itselfSally 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 geneticsAkira 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 stonesM 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 veinsWaheed-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 syndromeAkira Wiberg, Michael Ng, Annina B Schmid, et al.
BJS Open|July 23, 2025
Time to recovery following open and endoscopic carpal tunnel decompression: meta-analysisOlivia 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 studyBenjamin 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 activityYoshifumi Itoh, Michael Ng, Akira Wiberg, et al.
Pageof 4