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

Deborah Krakow

ORCID: 0000-0001-9906-4968
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 1%percentile
4.6Author 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.

Nosology of genetic skeletal disorders: 2023 revision

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63132
Top 5%
4.6DataRank
Top 5%379 citations

Carlos R. Ferreira, Geert Mortier, Houda Ali, Débora Romeo Bertola, Alistair Calder +16 more

Papers

Driven by 15 papers — median percentile 95. Top paper: “Nosology of genetic skeletal disorders: 2023 revision”.

Nosology of genetic skeletal disorders: 2023 revision

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63132
Top 5%
4.6DataRank
Top 5%379 citations

Carlos R. Ferreira, Geert Mortier, Houda Ali, Débora Romeo Bertola, Alistair Calder +16 more

The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery

Nature Genetics(2016)10.1038/ng.3558
N/A
0.776DataRank · unranked
175 citations

Michinori Toriyama, Chanjae Lee, S Paige Taylor, Iván Durán, Daniel H Cohn +27 more

Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling

EMBO Molecular Medicine(2020)10.15252/emmm.201911739
N/A
0.505DataRank · unranked
28 citations

Sara P. Abraham, Alexandru Niţă, Eva Hrubá, Marcela Buchtová, S. Paige Taylor +19 more

Innovations in MD-only physician-scientist training: experiences from the Burroughs Wellcome Fund physician-scientist institutional award initiative

Journal of Clinical Investigation(2021)10.1172/jci149948
N/A
0.330DataRank · unranked
8 citations

Jacqueline A. Hawkins-Salsbury, Vineet M. Arora, Mark T. Gladwin, James R. Goldenring, David P. Huston +12 more

Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1809
N/A
0DataRank · unranked
14 citations

Jessica Kianmahd, Meghna Singh, Maria F. Palafox, Angela Wei, Kathryn Elliott +40 more

4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta

Journal of Bone and Mineral Research(2020)10.1002/jbmr.4501
N/A
0DataRank · unranked
38 citations

Jennifer Zieba, Fabiana Csukasi, Jorge Martı́n, Davis Wachtell, Maya Barad +9 more

Altered Sox9 and FGF signaling gene expression in Aga2 OI mice negatively affects linear growth

JCI Insight(2023)10.1172/jci.insight.171984
N/A
0DataRank · unranked
8 citations

Lisette Nevarez, Davis Wachtell, Jorge Martı́n, Alexander Kot, Sereen Wong +3 more

Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling

PLoS Genetics(2023)10.1371/journal.pgen.1011005
N/A
0DataRank · unranked
12 citations

Bo Zhang, Megan Washington, I-Wen Song, Lindsay C. Burrage, Vittoria Rossi +28 more

Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome—osteogenesis imperfecta

Journal of Bone and Mineral Research(2024)10.1093/jbmr/zjae124
N/A
0DataRank · unranked
7 citations

Cora Chun, Jorge Martı́n, Davis Wachtell, David M. Hudson, MaryAnn Weis +7 more

Endoplasmic reticulum stress disrupts signaling via altered processing of transmembrane receptors

Cell Communication and Signaling(2025)10.1186/s12964-025-02208-w
N/A
0DataRank · unranked
6 citations

Sara P. Abraham, Davis Wachtell, Jennifer Zieba, Alexander Kot, Alexandru Niţă +18 more

Evidence-based classification of genes implicated in skeletal disorders using the ClinGen curation framework

Journal of Bone and Mineral Research(2025)10.1093/jbmr/zjaf183
N/A
0DataRank · unranked
0 citations

Hannah McCurry, Amanda Girod, Madeline Hughes, Emma H. Wilcox, Mayher Patel +23 more

Intervertebral disc degeneration is rescued by TGFβ/BMP signaling modulation in an ex vivo filamin B mouse model

Bone Research(2022)10.1038/s41413-022-00200-5
N/A
0DataRank · unranked
13 citations

Kimberly N. Forlenza, Kelly J. Heard, Jorge Martı́n, Michaela Kunova Bosakova, Daniel H. Cohn +4 more

Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia

EBioMedicine(2020)10.1016/j.ebiom.2020.103075
N/A
0DataRank · unranked
18 citations

Fabiana Csukasi, Michaela Kunova Bosakova, Jorge Martı́n, Wenjuan Zhang, S. Paige Taylor +10 more

Malocclusion traits and oral health–related quality of life in children with osteogenesis imperfecta

The Journal of the American Dental Association(2020)10.1016/j.adaj.2020.03.040
N/A
0DataRank · unranked
24 citations

Sreenath Madathil, Frank Rauch, V. Reid Sutton, Brendan Lee, Jean-Marc Retrouvey +19 more

Osteogenesis imperfecta tooth level phenotype analysis: Cross-sectional study

Bone(2021)10.1016/j.bone.2021.115917
N/A
0DataRank · unranked
19 citations

Hanan Moussa, Timothy Schwinghamer, Maxime Ducret, Didem Dagdeviren, Jean-Marc Retrouvey +23 more