Search research articles
Contact Us
Filters
Showing results (11-20 of 24) with videos related to
Page
of 3
Sort By:
NPJ Genomic Medicine
|
August 9, 2023
Familial co-segregation and the emerging role of long-read sequencing to re-classify variants of uncertain significance in inherited retinal diseases
Pankhuri Gupta, Kenji Nakamichi, Alyssa C Bonnell, et al.
Plant Science : an International Journal of Experimental Plant Biology
|
May 30, 2018
Modulations in primary and secondary metabolic pathways and adjustment in physiological behaviour of Withania somnifera under drought stress
Ruchi Singh, Pankhuri Gupta, Furqan Khan, et al.
Ophthalmology Science
|
April 10, 2025
Genetic Reasons for Phenotypic Diversity in Neuronal Ceroid Lipofuscinoses and High-Resolution Imaging as a Marker of Retinal Disease
Jennifer Huey, Pankhuri Gupta, Benjamin Wendel, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
Not Forgotten: Patient Experiences with Genetic Variant Reclassifications
Pankhuri Gupta, Min Seon Park, Eric Y Kao, et al.
ACS Applied Materials & Interfaces
|
August 3, 2022
Spin Pumping through Different Spin-Orbit Coupling Interfaces in β-W/Interlayer/Co<sub>2</sub>FeAl Heterostructures
Soumyarup Hait, Sajid Husain, Himanshu Bangar, et al.
Nano Letters
|
December 13, 2023
Magnetic-Proximity-Induced Efficient Charge-to-Spin Conversion in Large-Area PtSe<sub>2</sub>/Ni<sub>80</sub>Fe<sub>20</sub> Heterostructures
Richa Mudgal, Alka Jakhar, Pankhuri Gupta, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
MaveMD: A functional data resource for genomic medicine
Abbye E McEwen, Jeremy Stone, Malvika Tejura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 21, 2025
Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassifications
Andrew Folta, Adriana E Sedeño Cortés, Pankhuri Gupta, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Saturation genome editing of <i>BARD1</i> resolves VUS and provides insight into BRCA1-BARD1 tumor suppression
Ivan Woo, Silvia Casadei, Matthew W Snyder, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
Editing stem cell genomes at scale to measure variant effects in diverse cell and genetic contexts
Shawn Fayer, Riddhiman K Garge, Melissa Hopkins, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
NPJ Genomic Medicine
|
August 9, 2023
Familial co-segregation and the emerging role of long-read sequencing to re-classify variants of uncertain significance in inherited retinal diseases
Pankhuri Gupta, Kenji Nakamichi, Alyssa C Bonnell, et al.
Plant Science : an International Journal of Experimental Plant Biology
|
May 30, 2018
Modulations in primary and secondary metabolic pathways and adjustment in physiological behaviour of Withania somnifera under drought stress
Ruchi Singh, Pankhuri Gupta, Furqan Khan, et al.
Ophthalmology Science
|
April 10, 2025
Genetic Reasons for Phenotypic Diversity in Neuronal Ceroid Lipofuscinoses and High-Resolution Imaging as a Marker of Retinal Disease
Jennifer Huey, Pankhuri Gupta, Benjamin Wendel, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 25, 2026
Not Forgotten: Patient Experiences with Genetic Variant Reclassifications
Pankhuri Gupta, Min Seon Park, Eric Y Kao, et al.
ACS Applied Materials & Interfaces
|
August 3, 2022
Spin Pumping through Different Spin-Orbit Coupling Interfaces in β-W/Interlayer/Co<sub>2</sub>FeAl Heterostructures
Soumyarup Hait, Sajid Husain, Himanshu Bangar, et al.
Nano Letters
|
December 13, 2023
Magnetic-Proximity-Induced Efficient Charge-to-Spin Conversion in Large-Area PtSe<sub>2</sub>/Ni<sub>80</sub>Fe<sub>20</sub> Heterostructures
Richa Mudgal, Alka Jakhar, Pankhuri Gupta, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
MaveMD: A functional data resource for genomic medicine
Abbye E McEwen, Jeremy Stone, Malvika Tejura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 21, 2025
Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassifications
Andrew Folta, Adriana E Sedeño Cortés, Pankhuri Gupta, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Saturation genome editing of <i>BARD1</i> resolves VUS and provides insight into BRCA1-BARD1 tumor suppression
Ivan Woo, Silvia Casadei, Matthew W Snyder, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
Editing stem cell genomes at scale to measure variant effects in diverse cell and genetic contexts
Shawn Fayer, Riddhiman K Garge, Melissa Hopkins, et al.
Page
of 3