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

Mark D. Fleming

Boston Children's Hospital

ORCID: 0000-0003-0948-4024

Also affiliated with Harvard University, Boston Children's Museum

MedicineNursingBiochemistry, 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 4%percentile
0.626Author DataRank

Indexed papers

2in 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 2 indexed papers 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.

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Blood(2021)10.1182/blood.2021012781
Top 32%
0.626DataRank
Top 32%21 citations

Gudrun Göhring, Dennis D. Hickstein, Katherine R. Calvo, Courtney D. DiNardo, Michael Dworzak +42 more

Papers

Driven by 20 papers — median percentile 68. Top paper: “Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells”.

Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells

Nature Genetics(2023)10.1038/s41588-023-01433-8
N/A
1.3DataRank · unranked
53 citations

Sonia M. Dubois, Frank A. Buquicchio, Yu-Hsin Hsieh, Kopal Garg, Pauline Kautz +25 more

Maternal Iron Deficiency Modulates Placental Transcriptome and Proteome in Mid-Gestation of Mouse Pregnancy

Journal of Nutrition(2021)10.1093/jn/nxab005
N/A
0.860DataRank · unranked
23 citations

Miguel A. Prado, Liang Sun, Shira Rockowitz, Piotr Sliz, Joao A. Paulo +3 more

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

Nature Communications(2021)10.1038/s41467-021-21588-4
N/A
0.780DataRank · unranked
180 citations

Kasiani C. Myers, James R. Bowman, Christopher J. Gibson, Nicholas D. Camarda, Elissa Furutani +38 more

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Blood(2021)10.1182/blood.2021012781
Top 32%
0.626DataRank
Top 32%21 citations

Gudrun Göhring, Dennis D. Hickstein, Katherine R. Calvo, Courtney D. DiNardo, Michael Dworzak +42 more

A study assessing the feasibility of randomization of pediatric and young adult patients between matched unrelated donor bone marrow transplantation and immune‐suppressive therapy for newly diagnosed severe aplastic anemia: A joint pilot trial of the North American Pediatric Aplastic Anemia Consortium and the Pediatric Transplantation and Cellular Therapy Consortium

Pediatric Blood & Cancer(2020)10.1002/pbc.28444
N/A
0.489DataRank · unranked
25 citations

Leslie Lehmann, Alison A. Bertuch, Ghadir Sasa, Timothy S. Olson, Taizo A. Nakano +13 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008
N/A
0.489DataRank · unranked
25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Histologic and Laboratory Characteristics of Symptomatic and Asymptomatic Castleman Disease in the Pediatric Population

American Journal of Clinical Pathology(2020)10.1093/ajcp/aqaa011
N/A
0.396DataRank · unranked
13 citations

Mark D. Fleming, Karen M. Chisholm

Distinct genetic pathways define pre-leukemic and compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.04.134692
N/A
0.292DataRank · unranked
6 citations

Kasiani C. Myers, James R. Bowman, Christopher J. Gibson, Nicholas D. Camarda, Elissa Furutani +38 more

Single-cell multi-omics reveals dynamics of purifying selection of pathogenic mitochondrial DNA across human immune cells

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.20.517242
N/A
0.233DataRank · unranked
3 citations

Sonia M. Dubois, Frank A. Buquicchio, Yu-Hsin Hsieh, Kopal Garg, Pauline Kautz +24 more

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595
N/A
0.104DataRank · unranked
1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

medRxiv(2024)10.1101/2024.12.22.24319370
N/A
0.104DataRank · unranked
1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +30 more

Alternative start codon selection shapes mitochondrial function during evolution, homeostasis, and disease

10.1101/2025.03.27.645657
N/A
0DataRank · unranked
0 citations

Yi Fei Tao, Matteo Di Bernardo, Ekaterina Khalizeva, Christopher J. Giuliano, Sebastian Lourido +3 more

ITK deficiency presenting as autoimmune lymphoproliferative syndrome

Journal of Allergy and Clinical Immunology(2020)10.1016/j.jaci.2020.06.019
N/A
0DataRank · unranked
14 citations

Mohammed F. Alosaimi, Claudia Djambas Khayat, Faris Jaber, Abduarahman Almutairi, Sarah Beaussant-Cohen +6 more

Congenital X‐linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6

American Journal of Hematology(2021)10.1002/ajh.26382
N/A
0DataRank · unranked
8 citations

Katelyn E. Gagne, Ellen M. Beauchamp, Jonathan Fogel, Aleksej Perlov, Mireia Sola +17 more

DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling

Science Immunology(2022)10.1126/sciimmunol.abi4611
N/A
0DataRank · unranked
51 citations

Kim S. Robinson, Kenneth Lay, Jasmine C. Wong, Ricardo Moreno Traspas, Nasrin Nabavizadeh +24 more

Prospective observational pilot study of quantitative light dosimetry in erythropoietic protoporphyria

Journal of the American Academy of Dermatology(2022)10.1016/j.jaad.2022.11.036
N/A
0DataRank · unranked
8 citations

Lina Rebeiz, Haya S. Raef, Rebecca Karp Leaf, Sarina B. Elmariah, Hetanshi Naik +12 more

Successful cord blood transplantation for del7q myelodysplastic syndrome in Pearson marrow pancreas syndrome

American Journal of Hematology(2023)10.1002/ajh.27107
N/A
0DataRank · unranked
4 citations

Sonia M. Dubois, Elad Jacoby, Paul L. Martin, Sumit Parikh, Mark D. Fleming +2 more

Advancing precision care in pregnancy through a treatable fetal findings list

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.011
N/A
0DataRank · unranked
10 citations

Michael Duyzend, Sophia Adelson, Julie Yeo, Mark D. Fleming, Rebecca Ganetzky +12 more

Alternative start codon selection shapes mitochondrial function and rare human diseases

Molecular Cell(2025)10.1016/j.molcel.2025.10.013
N/A
0DataRank · unranked
6 citations

Matteo Di Bernardo, Yi Fei Tao, Ekaterina Khalizeva, Christopher J. Giuliano, Sebastian Lourido +3 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100441
N/A
0DataRank · unranked
1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +31 more