Settara C Chandrasekharappa

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 11

Top Venues

National Institutes of Health

Indian Institute of Science (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institutes of Health

United States

Staff Scientist/Associate Investigator :: National Human Genome Research Institute

Education History

Indian Institute of Science

India

PHD :: Biochemistry

Bangalore University

India

MSC :: Chemistry

Bangalore University

India

BSC :: Chemistry

Karantak university

India

BSC :: Chemistry

Publications

Ramanagouda Ramanagoudr-Bhojappa, Rebecca K Tryon, Francis P Lach, Frank X Donovan, Rochelle R Maxwell, Allana Rosenberg, Margaret L MacMillan, John E Wagner, Arleen D Auerbach, Agata Smogorzewska, Settara C Chandrasekharappa
FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia. Blood advances 8 (4) (2024)
Settara C Chandrasekharappa, Ramanagouda Ramanagoudr-Bhojappa, Francis P Lach, Frank X Donovan, Rochelle R Maxwell, Allana Rosenberg, Margaret L MacMillan, John E Wagner, Arleen D Auerbach, Agata Smogorzewska, Rebecca K Tryon
FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia. Blood advances (2024)
Ramanagouda Ramanagoudr-Bhojappa, Rebecca K Tryon, Francis P Lach, Frank X Donovan, Rochelle R Maxwell, Allana Rosenberg, Margaret L MacMillan, John E Wagner, Arleen D Auerbach, Agata Smogorzewska, Settara C Chandrasekharappa
FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia. Blood advances (2024)
Ramanagouda Ramanagoudr-Bhojappa, Rebecca K Tryon, Francis P Lach, Frank X Donovan, Rochelle R Maxwell, Allana Rosenberg, Margaret L MacMillan, John E Wagner, Arleen D Auerbach, Agata Smogorzewska, Settara C Chandrasekharappa
FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia. Blood advances 8 (4) (2024)
Kai Yu, Natalie T Deuitch, Matthew Douglas Merguerian, Lea Cunningham, Joie Davis, Erica Bresciani, Jamie L Diemer, Elizabeth J Andrews, Alice Young, Frank X Donovan, Raman Sood, Kathleen Marie Craft, Shawn N Chong, Settara C Chandrasekharappa, May Christine V Malicdan, Paul P Liu
Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancy. Blood advances (2023)
Andrew L H Webster, Mathijs A Sanders, Krupa Patel, Ralf Dietrich, Raymond J Noonan, Francis P Lach, Ryan R White, Audrey Goldfarb, Kevin Hadi, Matthew M Edwards, Frank X Donovan, Remco M Hoogenboezem, Moonjung Jung, Sunandini Sridhar, Tom F Wiley, Olivier Fedrigo, Huasong Tian, Joel Rosiene, Thomas Heineman, Jennifer A Kennedy, Lorenzo Bean, Rasim O Rosti, Rebecca Tryon, Ashlyn-Maree Gonzalez, Allana Rosenberg, Ji-Dung Luo, Thomas S Carroll, Sanjana Shroff, Michael Beaumont, Eunike Velleuer, Jeff C Rastatter, Susanne I Wells, Jordi Surralles, Grover Bagby, Margaret L MacMillan, John E Wagner, Maria Cancio, Farid Boulad, Theresa Scognamiglio, Roger Vaughan, Kristin G Beaumont, Amnon Koren, Marcin Imielinski, Settara C Chandrasekharappa, Arleen D Auerbach, Bhuvanesh Singh, David I Kutler, Peter J Campbell, Agata Smogorzewska
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer. Nature (2022)
Raymond T Doty, Xing Fan, David J Young, Jialiu Liang, Komudi Singh, Zahra Pakbaz, Ronan Desmond, Sara K Young-Baird, Settara C Chandrasekharappa, Frank X Donovan, Susan R Phelps, Thomas Winkler, Cynthia E Dunbar, Janis L Abkowitz
Studies of a mosaic patient with DBA and chimeric mice reveal erythroid cell-extrinsic contributions to erythropoiesis. Blood 139 (23) (2022)
Frank X Donovan, Avani Solanki, Minako Mori, Niranjan Chavan, Merin George, Selvaa Kumar C, Yusuke Okuno, Hideki Muramastsu, Kenichi Yoshida, Akira Shimamoto, Akifumi Takaori-Kondo, Hiromasa Yabe, Seishi Ogawa, Seiji Kojima, Miharu Yabe, Ramanagouda Ramanagoudr-Bhojappa, Agata Smogorzewska, Sheila Mohan, Aruna Rajendran, Arleen D Auerbach, Minoru Takata, Settara C Chandrasekharappa, Babu Rao Vundinti
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India. Human mutation 41 (1) (2019)
Ramanagouda Ramanagoudr-Bhojappa, Blake Carrington, Mukundhan Ramaswami, Kevin Bishop, Gabrielle M Robbins, MaryPat Jones, Ursula Harper, Stephen C Frederickson, Danielle C Kimble, Raman Sood, Settara C Chandrasekharappa
Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility. PLoS genetics 14 (12) (2018)
May Christine V Malicdan, Thierry Vilboux, Bruria Ben-Zeev, Jennifer Guo, Aviva Eliyahu, Ben Pode-Shakked, Amir Dori, Sravan Kakani, Settara C Chandrasekharappa, Carlos R Ferreira, Natalia Shelestovich, Dina Marek-Yagel, Hadass Pri-Chen, Ilan Blatt, John E Niederhuber, Langping He, Camilo Toro, Robert W Taylor, John Deeken, Tal Yardeni, Douglas C Wallace, William A Gahl, Yair Anikster
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency. Human mutation 39 (1) (2017)
Danielle C Kimble, Francis P Lach, Siobhan Q Gregg, Frank X Donovan, Elizabeth K Flynn, Aparna Kamat, Alice Young, Meghana Vemulapalli, James W Thomas, James C Mullikin, Arleen D Auerbach, Agata Smogorzewska, Settara C Chandrasekharappa
A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human mutation 39 (2) (2017)

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Publication Activity (10 Years)

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Settara C Chandrasekharappa