Burak Altintas

Also affiliated with Washington University in St. Louis, National Institutes of Health Clinical Center

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 6 papers. Top paper: “Fanconi anaemia: A syndrome with distinct subgroups”.

Fanconi anaemia: A syndrome with distinct subgroups

British Journal of Haematology(2022)10.1111/bjh.18091

N/A

0.385DataRank · unranked

12 citations

Neelam Giri, Lisa J. McReynolds, Burak Altintas, Blanche P. Alter

Most Fanconi anemia heterozygotes are not at increased cancer risk: A genome-first DiscovEHR cohort population study

Genetics in Medicine(2023)10.1016/j.gim.2023.101042

N/A

0.292DataRank · unranked

6 citations

Burak Altintas, Jeremy S. Haley, Jung Kim, Mark Ramos, David J. Carey +3 more

Differential diagnosis of bone marrow failure syndromes guided by machine learning

Blood(2022)10.1182/blood.2022017518

N/A

0DataRank · unranked

33 citations

Eric Munger, Xiaoyang Ma, Emma M. Groarke, Youbao Tang, Bhavisha A. Patel +33 more

Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosis

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.31966

N/A

0DataRank · unranked

4 citations

Melissa A. Parisi, Burak Altintas, May Christine V. Malicdan, Thierry Vilboux, Jasmine Knoll +6 more

Investigation of cancer predisposition in Fanconi anemia heterozygotes: A DiscovEHR cohort population study.

Journal of Clinical Oncology(2023)10.1200/jco.2023.41.16_suppl.10589

N/A

0DataRank · unranked

0 citations

Burak Altintas, Jeremy S. Haley, Jung Kim, David J. Carey, Douglas R. Stewart +2 more

Detailed assessment of rare and common TERT variation in a family with a telomere biology disorder

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100536

N/A

0DataRank · unranked

1 citations

Oscar Flórez-Vargas, Burak Altintas, Marena R. Niewisch, Weiyin Zhou, Neelam Giri +13 more