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

Olaf A. Bodamer

Broad Institute

ORCID: 0000-0002-7847-552X

Also affiliated with Boston Children's Hospital, Harvard University, Boston Children's Museum

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 7%percentile
0.120Author 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.

Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches

热加工工艺(2022)10.1002/mds.28951
Top 71%
0.120DataRank
Top 71%1 citations

Olaf A. Bodamer, Roy W A Peake, Deborah Raymond, Susan Bressman, Rachel Saunders‐Pullman +1 more

Papers

Driven by 8 papers — median percentile 29. Top paper: “Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches”.

Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches

热加工工艺(2022)10.1002/mds.28951
Top 71%
0.120DataRank
Top 71%1 citations

Olaf A. Bodamer, Roy W A Peake, Deborah Raymond, Susan Bressman, Rachel Saunders‐Pullman +1 more

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature

European Journal of Human Genetics(2020)10.1038/s41431-020-0571-6
N/A
0DataRank · unranked
38 citations

Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, Julien Thévenon, Ange‐Line Bruel +60 more

Application of N-palmitoyl-O-phosphocholineserine for diagnosis and assessment of response to treatment in Niemann-Pick type C disease

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.01.007
N/A
0DataRank · unranked
37 citations

Pamela Kell, Dennis J. Dietzen, Nicole Y. Farhat, An Dang, Forbes D. Porter +13 more

Neuroimaging in Kabuki syndrome and another KMT2D‐related disorder

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62450
N/A
0DataRank · unranked
14 citations

Margaret A. Kenna, Devon Barrett, Thomas E. Mullen, Olaf A. Bodamer, Pankaj B. Agrawal +3 more

Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)

Frontiers in Genetics(2022)10.3389/fgene.2022.867337
N/A
0DataRank · unranked
21 citations

Kee Chan, Marc S. Williams, Susan A. Berry, Robert J. Currier, Piero Rinaldo +22 more

Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107626
N/A
0DataRank · unranked
16 citations

Martin Caha, Leslie Smoot, David J. Harris, Amy E. Roberts, Stephanie Sacharow +2 more

Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)

Genetics in Medicine(2020)10.1038/s41436-020-0844-z
N/A
0DataRank · unranked
22 citations

Nina Mann, Makiko Nakayama, Dervla M. Connaughton, Rufeng Dai, Caroline M. Kolvenbach +17 more

KMT2D-deficiency destabilizes lineage progression in immature neural progenitors

Epigenetics Reports(2025)10.1080/28361512.2025.2599802
N/A
0DataRank · unranked
0 citations

Pushpinder Bawa, Feiya Wang, Sandra Sulser Ponce De Leon, Olaf A. Bodamer, H. Joseph Yost +2 more