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Louis Kunkel

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Current Opinion in Genetics & Development|June 22, 2002
The genetics of agingThomas Perls, Louis Kunkel, Annibale Puca
Proceedings of the National Academy of Sciences of the United States of America|June 13, 2002
Life-long sustained mortality advantage of siblings of centenariansThomas T Perls, John Wilmoth, Robin Levenson, et al.
BJU International|October 11, 2011
Genome gender diversity in affected sib-pairs with familial vesico-ureteric reflux identified by single nucleotide polymorphism linkage analysisGiovanni S Marchini, Bulent Onal, Chao-Yu Guo, et al.
European Journal of Human Genetics : EJHG|August 20, 2009
A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5Christine E Briggs, Chao-Yu Guo, Cynthia Schoettler, et al.
Plos One|April 19, 2012
The co-morbidity burden of children and young adults with autism spectrum disordersIsaac S Kohane, Andrew McMurry, Griffin Weber, et al.
Human Molecular Genetics|October 12, 2018
Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesisAnna Pakula, Angela Lek, Jeffrey Widrick, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome CohortElicia Estrella, Shira Rockowitz, Marielle Thorne, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Interstitial Cystitis: a phenotype and rare variant exome sequencing study: Interstitial Cystitis: a phenotype and exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
A slowly progressive form of limb-girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican HispanicsSamiah A Al-Zaidy, Vinod Malik, Kelley Kneile, et al.
Ebiomedicine|February 19, 2026
Interstitial cystitis: a phenotype and rare variant exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
Pageof 1

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

Sort By:
Pageof 1
Current Opinion in Genetics & Development|June 22, 2002
The genetics of agingThomas Perls, Louis Kunkel, Annibale Puca
Proceedings of the National Academy of Sciences of the United States of America|June 13, 2002
Life-long sustained mortality advantage of siblings of centenariansThomas T Perls, John Wilmoth, Robin Levenson, et al.
BJU International|October 11, 2011
Genome gender diversity in affected sib-pairs with familial vesico-ureteric reflux identified by single nucleotide polymorphism linkage analysisGiovanni S Marchini, Bulent Onal, Chao-Yu Guo, et al.
European Journal of Human Genetics : EJHG|August 20, 2009
A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5Christine E Briggs, Chao-Yu Guo, Cynthia Schoettler, et al.
Plos One|April 19, 2012
The co-morbidity burden of children and young adults with autism spectrum disordersIsaac S Kohane, Andrew McMurry, Griffin Weber, et al.
Human Molecular Genetics|October 12, 2018
Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesisAnna Pakula, Angela Lek, Jeffrey Widrick, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome CohortElicia Estrella, Shira Rockowitz, Marielle Thorne, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Interstitial Cystitis: a phenotype and rare variant exome sequencing study: Interstitial Cystitis: a phenotype and exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
Molecular Genetics & Genomic Medicine|March 25, 2015
A slowly progressive form of limb-girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican HispanicsSamiah A Al-Zaidy, Vinod Malik, Kelley Kneile, et al.
Ebiomedicine|February 19, 2026
Interstitial cystitis: a phenotype and rare variant exome sequencing studyJoshua E Motelow, Ayan Malakar, Sarath Babu Krishna Murthy, et al.
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