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

Michael L. Cunningham

Seattle Children's Hospital

ORCID: 0000-0003-2277-654X
Biochemistry, 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 2%percentile
2.0Author 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.

Chemical Effects in Biological Systems—Data Dictionary (CEBS-DD): A Compendium of Terms for the Capture and Integration of Biological Study Design Description, Conventional Phenotypes, and ‘Omics Data

Toxicological Sciences(2005)10.1093/toxsci/kfi315
Top 11%
2.0DataRank
Top 11%40 citations

Danielle Choi, Craig Zwickl, Norman Morrison, Asif Rashid, Atif Hasan +33 more

Papers

Driven by 28 papers — median percentile 89. Top paper: “Chemical Effects in Biological Systems—Data Dictionary (CEBS-DD): A Compendium of Terms for the Capture and Integration of Biological Study Design Description, Conventional Phenotypes, and ‘Omics Data”.

Chemical Effects in Biological Systems—Data Dictionary (CEBS-DD): A Compendium of Terms for the Capture and Integration of Biological Study Design Description, Conventional Phenotypes, and ‘Omics Data

Toxicological Sciences(2005)10.1093/toxsci/kfi315
Top 11%
2.0DataRank
Top 11%40 citations

Danielle Choi, Craig Zwickl, Norman Morrison, Asif Rashid, Atif Hasan +33 more

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.02.016
N/A
0.639DataRank · unranked
70 citations

Chloe Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick +91 more

Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

npj Genomic Medicine(2023)10.1038/s41525-022-00343-8
N/A
0.605DataRank · unranked
18 citations

Vikas Bhambhani, Nour Gazzaz, Mariska Davids, Paalini Sathiyaseelan, Ellen F. Macnamara +95 more

SMAD6 variants in craniosynostosis: genotype and phenotype evaluation

Genetics in Medicine(2020)10.1038/s41436-020-0817-2
N/A
0.593DataRank · unranked
51 citations

Araceli Cuellar, Krithi Bala, Sigrid M. A. Swagemakers, Nils Koelling, Simon J. McGowan +19 more

Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

The Journal of Experimental Medicine(2024)10.1084/jem.20232005
N/A
0.553DataRank · unranked
39 citations

Julian A. Yano, John Huizar, Leianna C. Slayden, Madeleine A. Weiss, Elizabeth A Turcotte +93 more

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Genetics in Medicine(2021)10.1038/s41436-020-01084-8
N/A
0.533DataRank · unranked
34 citations

Dustin Baldridge, Matt Velinder, Joel B. Krier, Kimberly LeBlanc, Cecilia Esteves +90 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Genetics in Medicine(2021)10.1038/s41436-021-01152-7
N/A
0.515DataRank · unranked
30 citations

Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London +95 more

Evidence for an acetoxyarylamine as the ultimate mutagenic reactive intermediate of the carcinogenic aromatic amine 2,4-diaminotoluene

Mutation Research/Genetic Toxicology(1990)10.1016/0165-1218(90)90035-z
N/A
0.510DataRank · unranked
29 citations

H.B. Matthews, Michael L. Cunningham

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Genetics in Medicine(2021)10.1038/s41436-021-01216-8
N/A
0.494DataRank · unranked
26 citations

Jennifer B. Phillips, Elizabeth L. Fieg, Sameer S. Bajikar, Judy Peirce, Jeremy Wegner +94 more

Damaging variants in FOXI3 cause microtia and craniofacial microsomia

Genetics in Medicine(2022)10.1016/j.gim.2022.09.005
N/A
0.464DataRank · unranked
21 citations

Andrew T. Timberlake, Justin J. Curran, Michael L. Cunningham, Barbara McDonough, Maria A. Artunduaga +21 more

The microRNA processorDROSHAis a candidate gene for a severe progressive neurological disorder

Human Molecular Genetics(2022)10.1093/hmg/ddac085
N/A
0.434DataRank · unranked
17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more

Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome

Brain(2022)10.1093/brain/awac223
N/A
0.434DataRank · unranked
17 citations

Aloran Mazumder, Daisuke Ogasawara, Rami Abou Jamra, Geneviève Bernard, Enrico Bertini +94 more

Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants

Disease Models & Mechanisms(2022)10.1242/dmm.049320
N/A
0.406DataRank · unranked
14 citations

Caleb Heffner, Timothy C. Cox, Michael L. Cunningham, Francisco A. Perez, Aaron M. Bauer +5 more

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in Medicine(2023)10.1016/j.gim.2023.100897
N/A
0.360DataRank · unranked
10 citations

Kelly Schoch, Rebecca Ganetzky, Peter G. Kranz, Neal Sondheimer, M. Louise Markert +92 more

De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

Genetics in Medicine(2023)10.1016/j.gim.2023.100833
N/A
0.359DataRank · unranked
6 citations

Jung-Wan Mok, Oguz Kanca, Sharayu Jangam, Cynthia J. Tifft, Ellen F. Macnamara +95 more

De novo variants in DENND5B cause a neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.001
N/A
0.345DataRank · unranked
9 citations

Valeria Tomati, Matteo P. Ferla, Mariateresa Lena, Julie S. Cohen, Ali Fatemi +94 more

Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

Scientific Reports(2024)10.1038/s41598-024-58343-w
N/A
0.241DataRank · unranked
4 citations

Cristina M. Justice, Zeynep Erdogan-Yildirim, Seppe Goovaerts, Araceli Cuellar, John R. Shaffer +16 more

A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

Genetics in Medicine(2022)10.1016/j.gim.2022.12.001
N/A
0.170DataRank · unranked
1 citations

Queenie K.‐G. Tan, Chloe Reuter, Kelly Schoch, Jennefer N. Kohler, Devon Bonner +94 more

AXIN1 mutations in nonsyndromic craniosynostosis

Journal of Neurosurgery Pediatrics(2024)10.3171/2024.5.peds24115
N/A
0.165DataRank · unranked
2 citations

Kshipra Hemal, Jonas A. Gustafson, Le Hao, Irene Valenzuela, Anne Slavotinek +5 more

Do Infant Motor Skills Mediate the Association Between Positional Plagiocephaly/Brachycephaly and Cognition in School-Aged Children?

Physical Therapy(2020)10.1093/ptj/pzaa214
N/A
0DataRank · unranked
8 citations

Erin R. Wallace, Cindy Ola, Deborah Kartin, Michael L. Cunningham, Matthew L. Speltz +1 more

Time-course comparison of xenobiotic activators of CAR and PPARα in mouse liver

UNC Libraries(2020)10.17615/4mc7-9v77
N/A
0DataRank · unranked
0 citations

Oksana Kosyk, Ivan Rusyn, Blair U. Bradford, Pamela K. Ross, Michael L. Cunningham +2 more

Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders

Journal of Medical Genetics(2021)10.1136/jmedgenet-2020-107459
N/A
0DataRank · unranked
10 citations

Maud Wurmser, Simon J. McGowan, Rodrigo Atique, Débora Romeo Bertola, Michael L. Cunningham +11 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012
N/A
0DataRank · unranked
38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

Sustained formation of POBN radical adducts in mouse liver by peroxisome proliferators is dependent upon PPARα, but not NADPH oxidase

UNC Libraries(2020)10.17615/0kjp-kh42
N/A
0DataRank · unranked
0 citations

Amanda Burns, Michael L. Cunningham, Blair U. Bradford, Maria B. Kadiiska, Akira Maki +5 more

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.012
N/A
0DataRank · unranked
8 citations

Rossella Venditti, Evangelos A. Theodorou, Lauren C. Briere, Marion Rosello, Alfonsina Tirozzi +94 more

Phenotypic Anchoring of Acetaminophen-Induced Oxidative Stress with Gene Expression Profiles in Rat Liver

UNC Libraries(2020)10.17615/pezj-mb81
N/A
0DataRank · unranked
0 citations

Christine L. Powell, Gary A. Boorman, Michael L. Cunningham, Alexandra N. Heinloth, James A. Swenberg +6 more

LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants

BMC Genomics(2024)10.1186/s12864-023-09935-9
N/A
0DataRank · unranked
0 citations

Camilo Toro, David R. Adams, Undiagnosed Diseases Network, Maria T. Acosta, Margaret P Adam +95 more

Haploinsufficiency of SF3B2 causes craniofacial microsomia

Nature Communications(2021)10.1038/s41467-021-24852-9
N/A
0DataRank · unranked
89 citations

Casey Griffin, Carrie L. Heike, Anne Hing, Michael L. Cunningham, David Chitayat +24 more