Frank X. Donovan

Also affiliated with University of Würzburg, National Human Genome Research Institute, Cancer Genetics (United States)

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 15 papers. Top paper: “Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy”.

Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy

Blood Advances(2023)10.1182/bloodadvances.2023011165

N/A

0.866DataRank · unranked

35 citations

Natalie Deuitch, Matthew Merguerian, Lea Cunningham, Joie Davis, Erica Bresciani +11 more

Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer

Nature(2022)10.1038/s41586-022-05253-4

N/A

0.673DataRank · unranked

88 citations

Mathijs A. Sanders, Krupa R. Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach +44 more

Pathogenic germline IKZF1 variant alters hematopoietic gene expression profiles

Molecular Case Studies(2021)10.1101/mcs.a006015

N/A

0.482DataRank · unranked

7 citations

Payal P. Khincha, Neelam Giri, Aaron J. Bouk, Mia Steinberg, Jieqiong Dai +10 more

FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia

Blood Advances(2024)10.1182/bloodadvances.2023011888

N/A

0.355DataRank · unranked

6 citations

Rebecca Tryon, Francis P. Lach, Frank X. Donovan, Rochelle R. Maxwell, Allana Rosenberg +6 more

AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

Neurobiology of Disease(2024)10.1016/j.nbd.2024.106537

N/A

0.273DataRank · unranked

5 citations

Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George G. Harmison +20 more

Somatic genetic rescue in ZCCHC8 -associated telomere biology disorders

Blood(2025)10.1182/blood.2025031248

N/A

0.208DataRank · unranked

3 citations

Flávia S. Donaires, Nicholas F. DeCleene, Ibrahima Ba, Mina Nouri, Laëtitia Kermasson +24 more

Polygenic Risk Scores and HLA Class II Variants are Biomarkers of Corticosteroid Response in Childhood Nephrotic Syndrome

medRxiv(2025)10.1101/2025.08.01.25332825

N/A

0DataRank · unranked

1 citations

Alejandro Ochoa, Amika Sood, Ashley Drabik, Megan Chryst-Stangl, Brandon M. Lane +43 more

Patient-derived xenograft models of Fanconi anemia–associated head and neck cancer identify personalized therapeutic strategies

Journal of Clinical Investigation(2025)10.1172/jci195334

N/A

0DataRank · unranked

0 citations

Hua Li, Benjamin A Harrison, Andrew Webster, Joanna Pucilowska, Austin Nguyen +21 more

Fanconi Anemia Pathway Deficiency Drives Copy Number Variation in Squamous Cell Carcinomas

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.14.456365

N/A

0DataRank · unranked

12 citations

Mathijs A. Sanders, Krupa R. Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach +39 more

Tracking Cytopenias in FANCA -deficient Fanconi Anemia

medRxiv(2025)10.64898/2025.12.14.25341731

N/A

0DataRank · unranked

0 citations

Tamar Berger, Caroline S. Jiang, Allana Rosenberg, Ashlyn-Maree Gonzalez, Jodie Odame +17 more

Studies of a mosaic patient with DBA and chimeric mice reveal erythroid cell–extrinsic contributions to erythropoiesis

Blood(2022)10.1182/blood.2021013507

N/A

0DataRank · unranked

15 citations

Xing Fan, David J. Young, Jialiu A. Liang, Komudi Singh, Zahra Pakbaz +9 more

ALDH9A1 Deficiency as a Source of Endogenous DNA Damage that Requires Repair by the Fanconi Anemia Pathway

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.26.493623

N/A

0DataRank · unranked

5 citations

Isaac Ilyashov, Yeji Park, Frank X. Donovan, Ramanagouda Ramanagoudr‐Bhojappa, Danielle Keahi +16 more

Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.012

N/A

0DataRank · unranked

20 citations

M. Gillis, Linnea Lundh, Laura L. Baxter, Julia C. Wedel, Dawn E. Watkins‐Chow +6 more

Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancy

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.17.524290

N/A

0DataRank · unranked

5 citations

Natalie Deuitch, Matthew Merguerian, Lea Cunningham, Joie Davis, Erica Bresciani +11 more

Persistent immune dysregulation and metabolic alterations following SARS-CoV-2 infection

medRxiv(2025)10.1101/2025.04.16.25325949

N/A

0DataRank · unranked

12 citations

Katherine Bricker-Holt, Joseph M. Rocco, Adam Rupert, Frank X. Donovan, Yevgeniya Abramzon +15 more