Kimberly A. Aldinger

Also affiliated with Norcliffe Foundation, Seattle University

MedicineBiochemistry, 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 1%percentile

13.1Author DataRank

Indexed papers

4in 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 4 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.

A human cell atlas of fetal gene expression

Science(2020)10.1126/science.aba7721

Top 3%

6.2DataRank

Top 3%842 citations

Diana R. O’Day, Hannah A. Pliner, Paul D. Kingsley, Mei Deng, Riza M. Daza +12 more

Papers

Driven by 31 papers — median percentile 81. Top paper: “A human cell atlas of fetal gene expression”.

A human cell atlas of fetal gene expression

Science(2020)10.1126/science.aba7721

Top 3%

6.2DataRank

Top 3%842 citations

Diana R. O’Day, Hannah A. Pliner, Paul D. Kingsley, Mei Deng, Riza M. Daza +12 more

A human cell atlas of fetal chromatin accessibility

Science(2020)10.1126/science.aba7612

Top 3%

5.8DataRank

Top 3%466 citations

Andrew J. Hill, Riza M. Daza, Junyue Cao, Diana R. O’Day, Hannah A. Pliner +12 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

European Journal of Human Genetics(2024)10.1038/s41431-024-01701-z

Top 34%

0.572DataRank

Top 34%16 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +69 more

Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain

Scientific Data(2020)10.1038/s41597-020-0527-2

Top 38%

0.505DataRank

Top 38%17 citations

Andrew E. Timms, James W. MacDonald, Hanna K. McNamara, Jennifer Herstein, Theo K. Bammler +4 more

Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling

Genetics in Medicine(2022)10.1016/j.gim.2022.07.005

N/A

0.477DataRank · unranked

23 citations

Rachel VanCoillie, Elizabeth VanSickle, Deanna Alexis Carere, Kara Withrow, Erin Torti +43 more

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Genetics in Medicine(2021)10.1038/s41436-021-01114-z

N/A

0DataRank · unranked

93 citations

Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia S. Gubbels +76 more

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain

Molecular Cell(2021)10.1016/j.molcel.2021.09.020

N/A

0DataRank · unranked

57 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +21 more

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain

Molecular Cell(2021)10.1016/j.molcel.2021.10.023

N/A

0DataRank · unranked

14 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +22 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

medRxiv(2021)10.1101/2021.09.06.21262776

N/A

0DataRank · unranked

8 citations

Felice D’Arco, Kimberly A. Aldinger, Constance Smith‐Hicks, Christiane Zweier, Gyri Aasland Gradek +64 more

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.30.437620

N/A

0DataRank · unranked

2 citations

Kimberly A. Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K. McNamara +17 more

Failure of human rhombic lip differentiation underlies medulloblastoma formation

Nature(2022)10.1038/s41586-022-05215-w

N/A

0DataRank · unranked

165 citations

Parthiv Haldipur, Olivier Saulnier, Jake Millman, Alexandria H. Sjoboen, Anders W. Erickson +95 more

Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders

Annual Review of Neuroscience(2022)10.1146/annurev-neuro-111020-091953

N/A

0DataRank · unranked

73 citations

Kathleen J. Millen, Kimberly A. Aldinger, Parthiv Haldipur

Generation of advanced cerebellar organoids for neurogenesis and neuronal network development

Human Molecular Genetics(2023)10.1093/hmg/ddad110

N/A

0DataRank · unranked

29 citations

Luke Andrew Dascenzo Bury, Chen Fu, Kimberly A. Aldinger, Helen C. Miranda, Anthony Wynshaw‐Boris +1 more

Macrocephaly and developmental delay caused by missense variants in RAB5C

Human Molecular Genetics(2023)10.1093/hmg/ddad130

N/A

0DataRank · unranked

4 citations

Weimin Yuan, Federico Tessadori, Wilmer R. Rodriguez-Polanco, Jeremy J. Grubbs, Bo Zhang +94 more

Differentiation latency, cell division symmetry, and dormancy signatures define fetal liver HSCs at single cell resolution

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.01.543314

N/A

0DataRank · unranked

0 citations

Juliane I Mercoli, Adam Heck, Ian G. Phelps, Barbara Varnum‐Finney, Stacey Dozono +13 more

Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome Sequencing

medRxiv(2023)10.1101/2023.09.11.23295207

N/A

0DataRank · unranked

0 citations

Lindsay V. Clark, Erdal Coşgun, Kimberly A. Aldinger, Andrew E. Timms, Lely A. Quina +13 more

Early rhombic lip Protogenin+ve stem cells in a human-specific neurovascular niche initiate and maintain group 3 medulloblastoma

Cell(2024)10.1016/j.cell.2024.06.011

N/A

0DataRank · unranked

33 citations

Olivier Saulnier, Chuan Chen, Parthiv Haldipur, Wilda Orisme, Alberto Delaidelli +59 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624

N/A

0DataRank · unranked

21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63596

N/A

0DataRank · unranked

6 citations

Lindsay V. Clark, Erdal Coşgun, Kimberly A. Aldinger, Andrew E. Timms, Lely A. Quina +13 more

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

UNC Libraries(2024)10.17615/2254-fj45

N/A

0DataRank · unranked

0 citations

Rolph Pfundt, Birgit Elisabeth Kristiansen, Mary J. Green, Sally Ann Lynch, Amanda Openshaw +67 more

Ontogeny Dictates Oncogenic Potential, Lineage Hierarchy, and Therapy Response in Pediatric Leukemia

Cancer Discovery(2025)10.1158/2159-8290.cd-25-0556

N/A

0DataRank · unranked

2 citations

Shayan Saniei, Nikita Poddar, Isabella G. Martinez, C. Chao, Subrina Persaud +45 more

Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.013

N/A

0DataRank · unranked

1 citations

Rosie Sullivan, Mischa S. G. Ruegg, Julia A. Horsfield, Jordan Doran, Gemma Poke +30 more

A clinical and genotype-phenotype analysis of MACF1 variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.010

N/A

0DataRank · unranked

1 citations

Rachel Schot, Kimberly A. Aldinger, David B. Everman, Camerun Washington, Julie R. Jones +85 more

Differentiation latency and dormancy signatures define fetal liver hematopoietic stem cells at single-cell resolution

Cell Reports(2025)10.1016/j.celrep.2025.116289

N/A

0DataRank · unranked

1 citations

Juliane I Mercoli, Adam Heck, Ian G. Phelps, Barbara Varnum‐Finney, Stacey Dozono +13 more

Missense variants in DPYSL5 associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro

Molecular Psychiatry(2025)10.1038/s41380-025-03364-8

N/A

0DataRank · unranked

1 citations

Solène Remizé, Liberty François‐Moutal, Dévina C. Ung, Audrey Dangoumau, Sylviane Marouillat +24 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

Epigenomic landscape of the developing human rhombic lip reveals gene regulatory network and non-coding loci of developmental, evolutionary, and disease relevance

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.30.685586

N/A

0DataRank · unranked

0 citations

Soumya V. Menon, Paul Wambo, Ilinca Lungu, Kimberly A. Aldinger, Shraddha Pai +1 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

Laser Capture Micro-dissection (LCM) of Neonatal Mouse Forebrain for RNA Isolation

BIO-PROTOCOL(2020)10.21769/bioprotoc.3475

N/A

0DataRank · unranked

2 citations

Mei Deng, Kimberly A. Aldinger, I. S. Glass, Kathleen J. Millen, Achira Roy

Disruption of RFX family transcription factors causes autism, attention deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

medRxiv(2020)10.1101/2020.09.09.20187104

N/A

0DataRank · unranked

9 citations

Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia S. Gubbels +71 more

Spatial and single-cell transcriptional landscape of human cerebellar development

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.30.174391

N/A

0DataRank · unranked

8 citations

Zach Thomson, Parthiv Haldipur, Mei Deng, Andrew E. Timms, Matthew Hirano +16 more

Kimberly A. Aldinger

Indexed papers

Top data-sharing exemplar

Papers