Frank X Donovan

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Topics

Childhood Cancer

Top Venues

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

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)