Eric W. Klee

Also affiliated with WinnMed, Mayo Clinic in Florida

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 100%percentile

0Author 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 →

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

Data from Identification of Prognostic Biomarkers for Prostate Cancer

(2023)10.1158/1078-0432.c.6518722

Top 100%

0DataRank

Top 100%0 citations

Jan Marie A. Munz, C. Dilara Savci‐Heijink, Craig Spiro, Eric W. Klee, Dagmar Marie Kube +6 more

Papers

Driven by 35 papers — median percentile 0. Top paper: “Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome”.

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.002

N/A

0.568DataRank · unranked

43 citations

Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong +95 more

A reverse genetics and genomics approach to gene paralog function and disease: Myokymia and the juxtaparanode

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.07.006

N/A

0.396DataRank · unranked

13 citations

Nina Kozar, Ruizhi Duan, stephen bradley, Kenji Yokochi, Fuad Al Mutairi +35 more

Epigenetic alteration contributes to the transcriptional reprogramming in T-cell prolymphocytic leukemia

Scientific Reports(2021)10.1038/s41598-021-87890-9

N/A

0.208DataRank · unranked

3 citations

Henan Zhang, Pan Zhang, Michael T. Kalmbach, Jeong‐Heon Lee, Tamás Ördög +9 more

Genomic epidemiology reveals the dominance of Hennepin County in the transmission of SARS-CoV-2 in Minnesota from 2020 to 2022

mSphere(2023)10.1128/msphere.00232-23

N/A

0.104DataRank · unranked

1 citations

Kimberly P. Lauer, Eric D. Wieben, Yesesri Cherukuri, Julie M. Cunningham, Eric W. Klee +15 more

Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome

Acta Neuropathologica(2020)10.1007/s00401-020-02223-w

N/A

0DataRank · unranked

46 citations

Edgard Verdura, Natalia Juliá‐Palacios, Eric N. Anderson, Leire Goicoechea, Laura Planas‐Serra +33 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

SPECC1L regulates palate development downstream of IRF6

Human Molecular Genetics(2020)10.1093/hmg/ddaa002

N/A

0DataRank · unranked

27 citations

Luke W. Wenger, Nathan R. Wilson, Sraavya S Undurty-Akella, Jennifer Standley, Eno-Abasi Augustine-Akpan +23 more

A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype

Haematologica(2020)10.3324/haematol.2020.259275

N/A

0DataRank · unranked

5 citations

Francis P. Lach, Kimberly A. Rickman, Alejandro Ferrer, Abhishek A. Mangaonkar, Tanya L. Schwab +10 more

Pathogenic SPTBN1 variants cause a novel autosomal dominant neurodevelopmental syndrome

medRxiv(2020)10.1101/2020.08.31.20184481

N/A

0DataRank · unranked

3 citations

Keith A. Breau, Blake A. Creighton, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +63 more

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

Nature Genetics(2021)10.1038/s41588-021-00886-z

N/A

0DataRank · unranked

108 citations

Blake A. Creighton, Keith A. Breau, Rebecca C. Spillmann, Erin Torti, Sruthi Dontu +70 more

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.015

N/A

0DataRank · unranked

93 citations

Kaifang Pang, Andrea Ciolfi, Michael A. Levy, Andrés Hernández, Lucia Pedace +95 more

Design considerations for workflow management systems use in production genomics research and the clinic

Scientific Reports(2021)10.1038/s41598-021-99288-8

N/A

0DataRank · unranked

33 citations

Joshua Allen, Tajesvi Bhat, Prakruthi Burra, Christina Fliege, Steven N. Hart +15 more

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.019

N/A

0DataRank · unranked

47 citations

Heidi Cope, Zelha Nil, Thomas A. Ravenscroft, Wu‐Lin Charng, Shenzhao Lu +42 more

A form of muscular dystrophy associated with pathogenic variants in JAG2

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.020

N/A

0DataRank · unranked

41 citations

Alison M. Barnard, Sanna Puusepp, Sander Pajusalu, Katrin Õunap, Dorianmarie Vargas‐Franco +53 more

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

Journal of Medical Genetics(2021)10.1136/jmedgenet-2021-107751

N/A

0DataRank · unranked

30 citations

Margot A. Cousin, Nikita R. Dsouza, Thomas D. Challman, Karen E. Wain, Zöe Powis +67 more

TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62347

N/A

0DataRank · unranked

20 citations

Alejandro Ferrer, Carla Nishimura, Filippo Pinto e Vairo, Tristan Rey, Bruno Leheup +27 more

Design considerations for workflow management systems use in production genomics research and the clinic

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.03.437906

N/A

0DataRank · unranked

5 citations

Joshua Allen, Tajesvi Bhat, Prakruthi Burra, Christina Fliege, Steven N. Hart +15 more

Pathogenic mutations in the chromokinesin KIF22 disrupt anaphase chromosome segregation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.29.462402

N/A

0DataRank · unranked

1 citations

Patrick R. Blackburn, Noah S Arons, Sarah N Stevens, Dusica Babovic‐Vuksanovic, Jane B. Lian +3 more

Luminal androgen receptor breast cancer subtype and investigation of the microenvironment and neoadjuvant chemotherapy response

NAR Cancer(2022)10.1093/narcan/zcac018

N/A

0DataRank · unranked

43 citations

Roberto A. Leon‐Ferre, Jason P. Sinnwell, David Zahrieh, Vera J. Suman, Filho Otto Metzger +15 more

Pathogenic mutations in the chromokinesin KIF22 disrupt anaphase chromosome segregation

eLife(2022)10.7554/elife.78653

N/A

0DataRank · unranked

23 citations

Patrick R. Blackburn, Noah S Arons, Sarah N Stevens, Dusica Babovic‐Vuksanovic, Jane B. Lian +3 more

Genomic epidemiology reveals the dominance of Hennepin County in transmission of SARS-CoV-2 in Minnesota from 2020-2022

medRxiv(2022)10.1101/2022.07.24.22277978

N/A

0DataRank · unranked

0 citations

Kimberly P. Lauer, Eric D. Wieben, Yesesri Cherukuri, Julie M. Cunningham, Eric W. Klee +15 more

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.006

N/A

0DataRank · unranked

37 citations

Tanya L. Schwab, Sarah K. Macklin‐Mantia, A. Reghan Foley, Filippo Pinto e Vairo, Davut Pehli̇van +25 more

Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

iScience(2023)10.1016/j.isci.2023.106818

N/A

0DataRank · unranked

33 citations

Kristian Assing, Safa Barış, Stephanie L. Safgren, Işık Somuncu Johansen, Marianne Antonius Jakobsen +20 more

Data from Identification of Prognostic Biomarkers for Prostate Cancer

(2023)10.1158/1078-0432.c.6518722

Top 100%

0DataRank

Top 100%0 citations

Jan Marie A. Munz, C. Dilara Savci‐Heijink, Craig Spiro, Eric W. Klee, Dagmar Marie Kube +6 more

Loss‐of‐Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder

Annals of Neurology(2024)10.1002/ana.27077

N/A

0DataRank · unranked

10 citations

Frédéric Ebstein, Tzung‐Chien Hsieh, Marialetizia Motta, Francesca Clementina Radio, Johanna C. Herkert +74 more

Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders

European Journal of Human Genetics(2024)10.1038/s41431-024-01576-0

N/A

0DataRank · unranked

5 citations

Kim Lee Ng, Filippo Pinto e Vairo, James Collins, Ronald D. Cohn, Kacie Riley +6 more

Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld‐Rieger Syndrome

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63542

N/A

0DataRank · unranked

4 citations

Cheryl L. Khanna, James B. Smadbeck, Sarah H. Johnson, Erick D. Bothun, Tyler Kaplan +12 more

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies

npj Genomic Medicine(2024)10.1038/s41525-024-00398-9

N/A

0DataRank · unranked

3 citations

Jeshurun C. Kalanithy, Gabriel C. Dworschak, Nina Ishorst, Enrico Mingardo, Filipa M. Lopes +66 more

Clonal dynamics of Richter transformation in chronic lymphocytic leukemia

Hematological Oncology(2024)10.1002/hon.3282

N/A

0DataRank · unranked

0 citations

Shulan Tian, Charla Secreto, Sutapa Sinha, Min Shi, Timothy G. Call +12 more

Individualized Medicine in the Era of Artificial Intelligence

Mayo Clinic Proceedings(2025)10.1016/j.mayocp.2025.07.028

N/A

0DataRank · unranked

2 citations

Eric W. Klee, Timothy B. Curry, Victor E. Ortega, William V. Bobo, Arjun P. Athreya +2 more

Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development

Neuron(2020)10.1016/j.neuron.2020.01.042

N/A

0DataRank · unranked

223 citations

Mariah L. Hoye, Ruiji Jiang, Bethany Johnson-Kerner, Lindsey Suit, Srivats Venkataramanan +49 more

Luminal androgen receptor breast cancer subtype and investigation of the microenvironment and neoadjuvant chemotherapy response

UNC Libraries(2025)10.17615/h225-mq92

N/A

0DataRank · unranked

0 citations

Daniel G. Stover, David Zahrieh, Matthew P. Goetz, Eric W. Klee, Lisa A. Carey +15 more

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Genetics in Medicine(2020)10.1038/s41436-020-00988-9

N/A

0DataRank · unranked

56 citations

Trine Bjørg Hammer, Elena Gardella, Danique R.M. Vlaskamp, Birgitte Bertelsen, Simone Mandelstam +80 more

Computational Detection of Known Pathogenic Gene Fusions in a Normal Tissue Database and Implications for Genetic Disease Research

Frontiers in Genetics(2020)10.3389/fgene.2020.00173

N/A

0DataRank · unranked

16 citations

Garrett Jenkinson, Eric W. Klee, Gavin R. Oliver

Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1477

N/A

0DataRank · unranked

18 citations

Ikuo Masuho, Filippo Pinto e Vairo, Christopher T. Schmitz, Tanya L. Schwab, Karl J. Clark +6 more

Eric W. Klee

Indexed papers

Top data-sharing exemplar

Papers