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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 21, 2025
Gaining a Genomic Foothold on Unexplained Kidney Failure
Janewit Wongboonsin, Michelle T McNulty, Matthew G Sampson
G3 (Bethesda, Md.)
|
December 10, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event
Christopher A Simeone, Michelle T McNulty, Yask Gupta, et al.
Kidney International
|
December 20, 2021
A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis
Michelle T McNulty, Damian Fermin, Felix Eichinger, et al.
Kidney International Reports
|
July 11, 2026
Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for Hematuria
Frida Lona-Durazo, Ian R Dinsmore, Michelle T McNulty, et al.
Biorxiv : the Preprint Server for Biology
|
December 22, 2025
The landscape of allele-specific expression in human kidneys
Ana C Onuchic-Whitford, Junmo Sung, Eric D Sakkas, et al.
American Journal of Human Genetics
|
July 31, 2018
An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome
Christopher E Gillies, Rosemary Putler, Rajasree Menon, et al.
Nature Communications
|
April 19, 2023
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs
Seong Kyu Han, Michelle T McNulty, Christopher J Benway, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 2, 2024
Recessive variants in the intergenic <i>NOS1AP-C1orf226</i> locus cause monogenic kidney disease responsive to anti-proteinuric treatment
Florian Buerger, Daanya Salmanullah, Lorrin Liang, et al.
Nature Communications
|
November 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment
Florian Buerger, Daanya Salmanullah, Lorrin Liang, et al.
Kidney International
|
June 20, 2020
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Xiaoyuan Jia, Tomohiko Yamamura, Rasheed Gbadegesin, et al.
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Search research articles
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Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 21, 2025
Gaining a Genomic Foothold on Unexplained Kidney Failure
Janewit Wongboonsin, Michelle T McNulty, Matthew G Sampson
G3 (Bethesda, Md.)
|
December 10, 2024
The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event
Christopher A Simeone, Michelle T McNulty, Yask Gupta, et al.
Kidney International
|
December 20, 2021
A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis
Michelle T McNulty, Damian Fermin, Felix Eichinger, et al.
Kidney International Reports
|
July 11, 2026
Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for Hematuria
Frida Lona-Durazo, Ian R Dinsmore, Michelle T McNulty, et al.
Biorxiv : the Preprint Server for Biology
|
December 22, 2025
The landscape of allele-specific expression in human kidneys
Ana C Onuchic-Whitford, Junmo Sung, Eric D Sakkas, et al.
American Journal of Human Genetics
|
July 31, 2018
An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome
Christopher E Gillies, Rosemary Putler, Rajasree Menon, et al.
Nature Communications
|
April 19, 2023
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs
Seong Kyu Han, Michelle T McNulty, Christopher J Benway, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 2, 2024
Recessive variants in the intergenic <i>NOS1AP-C1orf226</i> locus cause monogenic kidney disease responsive to anti-proteinuric treatment
Florian Buerger, Daanya Salmanullah, Lorrin Liang, et al.
Nature Communications
|
November 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment
Florian Buerger, Daanya Salmanullah, Lorrin Liang, et al.
Kidney International
|
June 20, 2020
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Xiaoyuan Jia, Tomohiko Yamamura, Rasheed Gbadegesin, et al.
Page
of 2