Publications by authors named "Nanda Singh"

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A Qualitative Analysis of Human-Animal Interactions with Respect to Zoonoses in Nepal.
Anna Durrance-Bagale, Hari Basnet, Nanda Bahadur Singh, Steven R Belmain, James W Rudge

Ecohealth· August 2025

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'Community people are the most powerful resources': qualitative critical realist analysis and framework to support co-produced responses to zoonotic disease threats with(in) Nepali communities.
Anna Durrance-Bagale, Hari Basnet, Nanda Bahadur Singh, Steven R Belmain, James W Rudge

BMC Public Health· April 2025

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Breeding ecology of the Asian openbill in eastern Nepal: Larger trees support higher fledgling success.
Ganesh Tamang, Hem Bahadur Katuwal, Asmit Subba, Nanda Bahadur Singh

Ecol Evol· June 2024

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A prospective case-control study of disability, quality of life, and functional impairment of shoulder movements after latissimus dorsi myocutaneous flap reconstruction in breast cancer patients.
Gitika Nanda Singh, Parijat Suryavanshi, Shariq Ahmad, Shubhajeet Roy

Turk J Surg· March 2024

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Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants.
Erin Mundt, Brent Mabey, Irene Rainville, Charite Ricker, Nanda Singh

Cancer Genet· November 2023

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Cancer Risk Associated With Pathogenic Variants Identified Using Multigene Hereditary Cancer Panel Testing.
Shelly Cummings, Andrew Alfonso, Elisha Hughes, Matt Kucera, Brent Mabey, Nanda Singh

JCO Precis Oncol· January 2023

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Subtilisin from Bacillus amyloliquefaciens induces apoptosis in breast cancer cells through ubiquitin-proteasome-mediated tubulin degradation.
Nanda Singh, Rima Tapader, Shruti Chatterjee, Ananda Pal, Amit Pal

Int J Biol Macromol· November 2022

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Drivers of zoonotic disease risk in the Indian subcontinent: A scoping review.
Anna Durrance-Bagale, James W Rudge, Nanda Bahadur Singh, Steven R Belmain, Natasha Howard

One Health· December 2021

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Germline Pathogenic Variants in the Ataxia Telangiectasia Mutated () Gene are Associated with High and Moderate Risks for Multiple Cancers.
Michael J Hall, Ryan Bernhisel, Elisha Hughes, Katie Larson, Eric T Rosenthal, Nanda A Singh

Cancer Prev Res (Phila)· April 2021

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Hereditary cancer testing challenges: assembling the analytical pieces to solve the patient clinical puzzle.
Karla R Bowles, Debora Mancini-DiNardo, Bradford Coffee, Hannah C Cox, Yaping Qian, Nanda Singh

Future Oncol· January 2019

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Prevalence of germ-line mutations in cancer genes among pancreatic cancer patients with a positive family history.
Kari G Chaffee, Ann L Oberg, Robert R McWilliams, Neil Majithia, Brian A Allen, Nanda Singh

Genet Med· January 2018

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Identification of pathogenic retrotransposon insertions in cancer predisposition genes.
Yaping Qian, Debora Mancini-DiNardo, Thaddeus Judkins, Hannah C Cox, Krystal Brown, Nanda Singh

Cancer Genet· October 2017

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Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Nanda Singh

J Clin Oncol· April 2017

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Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
Kari L Ring, Amanda S Bruegl, Brian A Allen, Eric P Elkin, Nanda Singh

Mod Pathol· November 2016

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Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
Nadine Tung, Nancy U Lin, John Kidd, Brian A Allen, Nanda Singh

J Clin Oncol· May 2016

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A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
Nanda A Singh, Chris Pappas, E Jill Dahle, Lieve R F Claes, Timothy H Pruess

PLoS Genet· September 2009

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Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes.
Timothy B Baker, Robert B Weiss, Daniel Bolt, Andrew von Niederhausern, Michael C Fiore, Nanda Singh

Nicotine Tob Res· July 2009

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Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions.
James F Otto, Nanda A Singh, E Jill Dahle, Mark F Leppert, Chris M Pappas

Epilepsia· July 2009

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Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
Nanda A Singh, James F Otto, E Jill Dahle, Chris Pappas, Jonathan D Leslie

J Physiol· July 2008

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A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.
Robert B Weiss, Timothy B Baker, Dale S Cannon, Andrew von Niederhausern, Diane M Dunn, Nanda A Singh

PLoS Genet· July 2008

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The Himalayas as a directional barrier to gene flow.
Tenzin Gayden, Alicia M Cadenas, Maria Regueiro, Nanda B Singh, Lev A Zhivotovsky

Am J Hum Genet· May 2007

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Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation.
Amy F Hubbard, E Wayne Askew, Nanda Singh, Mark Leppert, Paul S Bernstein

Arch Ophthalmol· February 2006

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TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study.
Hilary Coon, Nanda Singh, Diane Dunn, John H Eckfeldt, Michael A Province

Atherosclerosis· June 2004

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Nonsyndromic seizure disorders: epilepsy and the use of the internet to advance research.
Mark F Leppert, Nanda A Singh

Annu Rev Genomics Hum Genet· December 2003

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KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
Nanda A Singh, Peter Westenskow, Carole Charlier, Chris Pappas, Jonathan Leslie

Brain· December 2003

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