Settara Chandrasekharappa
10PUBLICATIONS
92CO-AUTHORS
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Publications (10)
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|Nov 25, 2025
Somatic genetic rescue in ZCCHC8-associated telomere biology disorders.Sophie de Tocqueville, Flavia Donaires, Nicholas DeCleene
|Sep 19, 2025
Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome.Tiffany Tu, Alejandro Ochoa, Amika Sood
|Jan 08, 2024
FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia.Ramanagouda Ramanagoudr-Bhojappa, Rebecca Tryon, Francis P Lach
|Nov 29, 2023
Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy.Kai Yu, Natalie Deuitch, Matthew Merguerian
|Nov 30, 2022
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.Andrew L H Webster, Mathijs A Sanders, Krupa Patel
|Mar 29, 2022
Studies of a mosaic patient with DBA and chimeric mice reveal erythroid cell-extrinsic contributions to erythropoiesis.Raymond T Doty, Xing Fan, David J Young
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Frequent Collaborators
7 joint publications
Frank X Donovan
3 joint publications
Agata Smogorzewska
2 joint publications
Adebowale Adeyemo
2 joint publications
Rasheed Gbadegesin
2 joint publications
Arleen D Auerbach
2 joint publications
Raman Sood
2 joint publications
Ramanagouda Ramanagoudr-Bhojappa
1 joint publications
Blake Carrington
1 joint publications
Mukundhan Ramaswami
1 joint publications
Gabrielle M Robbins
