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Ravi Mandla

Showing results (41-50 of 51) with videos related to

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Nature Genetics|March 26, 2025
Author Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature Genetics|October 22, 2024
Publisher Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Multi-omics characterization of type 2 diabetes associated genetic variationRavi Mandla, Kim Lorenz, Xianyong Yin, et al.
The Lancet. Diabetes & Endocrinology|April 30, 2026
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestriesAlicia Huerta-Chagoya, Joohyun Kim, Ravi Mandla, et al.
Diabetologia|May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Science (New York, N.Y.)|February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variantsHongbo Liu, Amin Abedini, Eunji Ha, et al.
Communications Biology|September 24, 2025
Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) programChloé Sarnowski, Yixin Zhang, Farah Ammous, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestriesAlicia Huerta-Chagoya, Joohyun Kim, Ravi Mandla, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complicationsKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Nature Genetics|March 26, 2025
Author Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature Genetics|October 22, 2024
Publisher Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Multi-omics characterization of type 2 diabetes associated genetic variationRavi Mandla, Kim Lorenz, Xianyong Yin, et al.
The Lancet. Diabetes & Endocrinology|April 30, 2026
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestriesAlicia Huerta-Chagoya, Joohyun Kim, Ravi Mandla, et al.
Diabetologia|May 6, 2023
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetesAlicia Huerta-Chagoya, Philip Schroeder, Ravi Mandla, et al.
Nature Communications|October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with heightGareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Science (New York, N.Y.)|February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variantsHongbo Liu, Amin Abedini, Eunji Ha, et al.
Communications Biology|September 24, 2025
Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) programChloé Sarnowski, Yixin Zhang, Farah Ammous, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestriesAlicia Huerta-Chagoya, Joohyun Kim, Ravi Mandla, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complicationsKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.
Pageof 6