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The New England Journal of Medicine
|
October 28, 2024
<i>APOL1</i> Bi- and Monoallelic Variants and Chronic Kidney Disease in West Africans
Rasheed A Gbadegesin, Ifeoma Ulasi, Samuel Ajayi, et al.
American Journal of Human Genetics
|
April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Nature Communications
|
April 29, 2023
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, Michelle T McNulty, Xiaoyuan Jia, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
American Journal of Human Genetics
|
January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
Patricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle McNulty, et al.
Nature Communications
|
November 30, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle T McNulty, et al.
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Search research articles
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Showing results (161-170 of 167) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 167 results.
The New England Journal of Medicine
|
October 28, 2024
<i>APOL1</i> Bi- and Monoallelic Variants and Chronic Kidney Disease in West Africans
Rasheed A Gbadegesin, Ifeoma Ulasi, Samuel Ajayi, et al.
American Journal of Human Genetics
|
April 2, 2024
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
Nature Communications
|
April 29, 2023
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, Michelle T McNulty, Xiaoyuan Jia, et al.
Medrxiv : the Preprint Server for Health Sciences
|
October 24, 2023
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, et al.
American Journal of Human Genetics
|
January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
Patricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle McNulty, et al.
Nature Communications
|
November 30, 2023
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J Friedman, Michelle T McNulty, et al.
Page
of 17