🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Alan Cantor

Boston Children's Hospital

ORCID: 0000-0002-5136-028X

Also affiliated with Harvard University, Dana-Farber Cancer Institute, Boston Children's Museum

MedicineBiochemistry, Genetics and Molecular Biology

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 3%percentile
1.3Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

Haematologica(2021)10.3324/haematol.2021.278762
Top 16%
1.3DataRank
Top 16%55 citations

Sarah L. King‐Smith, David Lawrence, Peer Arts, Jinghua Feng, James Andrews +38 more

Papers

Driven by 10 papers — median percentile 84. Top paper: “The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy”.

The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

Haematologica(2021)10.3324/haematol.2021.278762
Top 16%
1.3DataRank
Top 16%55 citations

Sarah L. King‐Smith, David Lawrence, Peer Arts, Jinghua Feng, James Andrews +38 more

Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript

The Journal of Experimental Medicine(2021)10.1084/jem.20210444
N/A
1.1DataRank · unranked
32 citations

Jeffrey M. Verboon, Leif S. Ludwig, Susan Black, Wendy Luo, Kopal Garg +13 more

CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation

Proceedings of the National Academy of Sciences(2020)10.1073/pnas.2003228117
N/A
1.1DataRank · unranked
25 citations

Hsuan-Ting Huang, Chung-Tsai Lee, Avik Choudhuri, Nicola K. Wilson, Brian J. Abraham +32 more

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

Cancer(2005)10.1002/cncr.21536
N/A
0.981DataRank · unranked
690 citations

Jenny Permuth‐Wey, Judith A. Betts, Jeffrey P. Krischer, James Fiorica, Hector Arango +13 more

Infantile Myelofibrosis and Myeloproliferation with CDC42Dysfunction

Journal of Clinical Immunology(2020)10.1007/s10875-020-00778-7
N/A
0DataRank · unranked
33 citations

Dilnar Mahmut, Ah Ram Kim, Mitsutoshi Nakamura, Nour J. Abdulhay, Satish K. Nandakumar +15 more

Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits

Nature Genetics(2020)10.1038/s41588-020-00738-2
N/A
0DataRank · unranked
49 citations

Eirini Trompouki, Brian J. Abraham, Leandro M. Colli, Kian Hong Kock, William Mallard +28 more

A phase II study of continuous oral mTOR inhibitor everolimus for recurrent, radiographic-progressive neurofibromatosis type 1–associated pediatric low-grade glioma: a Neurofibromatosis Clinical Trials Consortium study

Neuro-Oncology(2020)10.1093/neuonc/noaa071
N/A
0DataRank · unranked
82 citations

Sanjay P. Prabhu, Alyssa Reddy, Michael J. Fisher, Roger J. Packer, Stewart Goldman +15 more

Germline GATA1s-generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotype

Blood(2021)10.1182/blood.2021011463
N/A
0DataRank · unranked
28 citations

Ronald M. Kline, Eigil Kjeldsen, Nik F. Nik-Abdul-Rashid, Deepa Bhojwani, Jeffrey M. Verboon +9 more

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41

Blood Advances(2023)10.1182/bloodadvances.2023010045
N/A
0DataRank · unranked
40 citations

Michael W. Drazer, Kai Yu, David Lawrence, Jinghua Feng, Luis Arriola‐Martinez +60 more

Protocol optimization improves the performance of multiplexed RNA imaging

Scientific Reports(2025)10.1038/s41598-025-17477-1
N/A
0DataRank · unranked
3 citations

Christian A. Lochbaum, Paolo Cadinu, Rosalind J. Xu, Jose Aceves-Salvador, Evangelia Semizoglou +6 more