Michael C. Kruer

Also affiliated with University of Arizona, Phoenix Children's Hospital

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 5%percentile

0.373Author DataRank

Indexed papers

3in 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 3 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 →

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

Motor network dynamic resting state fMRI connectivity of neurotypical children in regions affected by cerebral palsy

Frontiers in Human Neuroscience(2024)10.3389/fnhum.2024.1339324

Top 65%

0.208DataRank

Top 65%3 citations

Bethany L. Sussman, Laura de Lima Xavier, Sarah N. Wyckoff, William Reuther, Michael C. Kruer +3 more

Papers

Driven by 34 papers — median percentile 30. Top paper: “Motor network dynamic resting state fMRI connectivity of neurotypical children in regions affected by cerebral palsy”.

Motor network dynamic resting state fMRI connectivity of neurotypical children in regions affected by cerebral palsy

Frontiers in Human Neuroscience(2024)10.3389/fnhum.2024.1339324

Top 65%

0.208DataRank

Top 65%3 citations

Bethany L. Sussman, Laura de Lima Xavier, Sarah N. Wyckoff, William Reuther, Michael C. Kruer +3 more

Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive

Journal of Clinical Investigation(2025)10.1172/jci189830

Top 70%

0.165DataRank

Top 70%2 citations

Khaing Phyu Aung, Vivian W. Y. Liao, Nathan L. Absalom, Han Chow Chua, Xuetao Gan +46 more

Insights From Genetic Studies of Cerebral Palsy

Frontiers in Neurology(2021)10.3389/fneur.2020.625428

N/A

0DataRank · unranked

49 citations

Sheetal Shetty, Bryce A. Wilson, Aris J. Huang, Sheng Chih Jin, Hayley Smithers‐Sheedy +3 more

ALG13 X‐linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes

Journal of Inherited Metabolic Disease(2021)10.1002/jimd.12378

N/A

0DataRank · unranked

29 citations

Miao He, Andrew C. Edmondson, Earnest James Paul Daniel, Jie Chen, Tyhiesia Donald +21 more

Mutation in ZDHHC15 Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual Disability

Neurology Genetics(2021)10.1212/nxg.0000000000000602

N/A

0DataRank · unranked

11 citations

Somayeh Bakhtiari, Jennifer Heim, Patricia Cornejo, James Liu, Aris J. Huang +6 more

Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy

Neurology Genetics(2021)10.1212/nxg.0000000000000583

N/A

0DataRank · unranked

8 citations

Abbas Tafakhori, Sheng Chih Jin, Brandon S. Guida, Elham Alehabib, Saghar Firouzbadi +5 more

Dynamic Resting State Motor Network Connectivity of Neurotypical Children, the Groundwork for Network-Guided Therapy in Childhood Movement Disorders

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.30.470606

N/A

0DataRank · unranked

4 citations

Sarah N. Wyckoff, Justin M. Fine, Jennifer Heim, Angus A. Wilfong, P. David Adelson +3 more

Mendelian etiologies identified with whole exome sequencing in cerebral palsy

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51506

N/A

0DataRank · unranked

82 citations

Dustin L. Gable, Jamie Love‐Nichols, Alexa Tsao, Shira Rockowitz, Piotr Sliz +34 more

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice

Nature Communications(2022)10.1038/s41467-022-31566-z

N/A

0DataRank · unranked

39 citations

Kyung Ah Han, Dongwook Kim, Gyubin Jang, Somayeh Bakhtiari, Dongseok Lim +35 more

SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance

Human Molecular Genetics(2022)10.1093/hmg/ddac114

N/A

0DataRank · unranked

17 citations

Martina Schaettin, Médéric Jeanne, Veranika Panasenkava, Anne‐Sophie Denommé‐Pichon, Boris Keren +43 more

Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly

Brain(2022)10.1093/brain/awac074

N/A

0DataRank · unranked

15 citations

J. Pedro Fernández-Murray, Mahtab Tavasoli, Heinrich Sticht, Gisela Stoltenburg‐Didinger, Leila Motlagh Scholle +24 more

Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia

Annals of Neurology(2022)10.1002/ana.26381

N/A

0DataRank · unranked

9 citations

Isabella Herman, Reza Maroofian, Aren E. Marshall, Karina Carvalho Donis, Jawid M. Fatih +60 more

AGAP1-associated endolysosomal trafficking abnormalities link gene–environment interactions in neurodevelopmental disorders

Disease Models & Mechanisms(2023)10.1242/dmm.049838

N/A

0DataRank · unranked

11 citations

Somayeh Bakhtiari, Jacob Forstrom, Allan Bayat, Frédéric Bilan, Gwenaël Le Guyader +5 more

Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a neurodevelopmental disorder characterized by developmental delay, intellectual disability and autistic features

Human Molecular Genetics(2023)10.1093/hmg/ddad124

N/A

0DataRank · unranked

7 citations

Baozhong Xin, Iris Nira Smith, Valerie Sency, Julia Szekely, Anna Alkelai +49 more

TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions

Brain(2023)10.1093/brain/awad301

N/A

0DataRank · unranked

7 citations

Sara A. Lewis, Somayeh Bakhtiari, Sandra H. Nordlie, Alex M. Pagnozzi, Helen Magee +55 more

A transposase-derived gene required for human brain development

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.28.538770

N/A

0DataRank · unranked

7 citations

Sara A. Lewis, Rodrigo Lopez Gutierrez, Makiko Yamada, Elias Rodríguez-Fos, Mercè Planas-Fèlix +36 more

Clinical actionability of genetic findings in cerebral palsy

medRxiv(2023)10.1101/2023.09.08.23295195

N/A

0DataRank · unranked

4 citations

Maya Chopra, Julie S. Cohen, Jennifer Bain, Bhooma R. Aravamuthan, Jason B. Carmel +10 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Research Square(2023)10.21203/rs.3.rs-3317938/v1

N/A

0DataRank · unranked

4 citations

Ghayda Mirzaa, Keqin Yan, Raissa Relator, Sara Timpano, Binnaz Yalcin +57 more

AGAP1-associated endolysosomal trafficking abnormalities link gene-environment interactions in a neurodevelopmental disorder

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.31.526497

N/A

0DataRank · unranked

2 citations

Somayeh Bakhtiari, Jacob Forstrom, Allan Bayat, Frédéric Bilan, Gwenaël Le Guyader +5 more

Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.51942

N/A

0DataRank · unranked

9 citations

Dustin L. Gable, Zoë Frazier, Abigail Sveden, Aisling Quinlan, Maya Chopra +5 more

Potential clinical applications of advanced genomic analysis in cerebral palsy

EBioMedicine(2024)10.1016/j.ebiom.2024.105229

N/A

0DataRank · unranked

3 citations

Andrew Ruttenberg, Tuğçe Iyiyol, Nahyun Kong, Sheng Chih Jin, Michael C. Kruer +1 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

An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.09.574708

N/A

0DataRank · unranked

3 citations

Leqian Yu, Barbara Vona, Dayea Park, Yulei Wei, Daniel A. Schmitz +30 more

eIF2α phosphorylation evokes dystonia-like movements with D2-receptor and cholinergic origin and abnormal neuronal connectivity

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.14.594240

N/A

0DataRank · unranked

2 citations

Jacob Forstrom, Jennifer Renee Tavani, Robert J. Schafer, Zach Tiede, Sergio Padilla‐Lopez +2 more

Motor network dynamic resting state fMRI connectivity of neurotypical children in regions affected by cerebral palsy

UNC Libraries(2024)10.17615/dvdq-4y72

Top 100%

0DataRank

Top 100%0 citations

Michael C. Kruer, William Reuther, Sarah N. Wyckoff, Laura de Lima Xavier, Justin M. Fine +3 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Nature Communications(2025)10.1038/s41467-025-64838-5

N/A

0DataRank · unranked

4 citations

Keqin Yan, Raissa Relator, Mathieu Lévesque, P.S. Jayasinghe, Sara Timpano +61 more

Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder

Brain(2025)10.1093/brain/awaf212

N/A

0DataRank · unranked

3 citations

M. Kathryn Barton, Katherine A. Lynch, Ashish R. Deshwar, Philip D. Campbell, Josephine Millard +49 more

LONP1 Variants Are Associated With Clinically Diverse Phenotypes

Clinical Genetics(2025)10.1111/cge.70057

N/A

0DataRank · unranked

1 citations

Lu Qiao, Rebecca Hernan, David A. Sweetser, Jessica L. Waxler, Daryl A. Scott +34 more

Further Delineation of the AUTS2 HX Repeat Domain‐Related Phenotype

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64093

N/A

0DataRank · unranked

2 citations

Chi Vicky Cheng, Stefano Giuseppe Caraffi, Ivan Ivanovski, Gianluca Piatelli, Edoardo Errichiello +29 more

PANK2-mediated de novo CoA synthesis is required for metabolic switching to fatty acid oxidation

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.07.680981

N/A

0DataRank · unranked

0 citations

Robert J. Schafer, Adam J. Rauckhorst, Ana M Santos-Exposito, Andrés Prieto-Rodríguez, Bryce A. Wilson +8 more

Combined Dietary Restriction and Chelation Therapy Reduces Manganese Burden in SLC39A14 ‐Associated Manganism

Movement Disorders(2025)10.1002/mds.70085

N/A

0DataRank · unranked

0 citations

Peter T. Skidmore, Brielle Edwards, Jennifer Heim, James Kelbert, Nathan Evans +7 more

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy

medRxiv(2025)10.1101/2025.11.04.25339178

N/A

0DataRank · unranked

0 citations

Yung-Chun Wang, Peter T. Skidmore, Carolina I. Galaz-Montoya, Sara A. Lewis, Bader Alhaddad +52 more

Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy

Human Mutation(2020)10.1002/humu.24015

N/A

0DataRank · unranked

40 citations

Katherine L. Helbig, Candace T. Myers, Marcello Scala, Robert Huether, Sara A. Lewis +40 more

Michael C. Kruer

Indexed papers

Top data-sharing exemplar

Papers