Elliott H. Sherr

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 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 →

Papers

Driven by 27 papers. Top paper: “Mapping of Unconventional Myosins in Mouse and Human”.

Mapping of Unconventional Myosins in Mouse and Human

Genomics(1996)10.1006/geno.1996.0488

N/A

5.4DataRank · unranked

78 citations

Joseph F. Skowron, Debra J. Gilbert, Karen B. Avraham, William L. Perry, William M. Bement +10 more

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207

N/A

0.691DataRank · unranked

99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

npj Genomic Medicine(2023)10.1038/s41525-023-00353-0

N/A

0.568DataRank · unranked

43 citations

Shannon Rego, Nuriye Sahin‐Hodoglugil, Mark Kvale, Billie R. Lianoglou, Tiffany Yip +33 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

Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum

NeuroImage(2020)10.1016/j.neuroimage.2020.116868

N/A

0DataRank · unranked

32 citations

Laura R. Fenlon, Ryan J. Dean, Jens Bunt, Elliott H. Sherr, Linda J. Richards +1 more

DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.29.227827

N/A

0DataRank · unranked

2 citations

Timothy J. Edwards, Eric Rider, Dorothy M. Jones, Jonathan W. C. Lim, Kok‐Siong Chen +9 more

The DCC receptor regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.03.233593

N/A

0DataRank · unranked

0 citations

Ilan Gobius, Ashley P.L. Marsh, Rodrigo Suárez, Caitlin R. Bridges, Yunan Ye +15 more

Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.003

N/A

0DataRank · unranked

46 citations

Maya M. Polovitskaya, Héctor Gaitán‐Peñas, Sara Bertelli, Grace E. VanNoy, P. Ellen Grant +34 more

DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation

eLife(2021)10.7554/elife.61618

N/A

0DataRank · unranked

20 citations

Timothy J. Edwards, Eric Rider, Dorothy M. Jones, Jonathan W. C. Lim, Kok‐Siong Chen +9 more

Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.024

N/A

0DataRank · unranked

17 citations

Shabab B. Hannan, Sarah Dyack, Sara MacKay, Ulrich A. Schatz, Martin Fleger +41 more

DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation

eLife(2021)10.7554/elife.61769

N/A

0DataRank · unranked

14 citations

Ilan Gobius, Ashley P.L. Marsh, Rodrigo Suárez, Jonathan W. C. Lim, Caitlin R. Bridges +16 more

Autism-associated biomarkers: test–retest reliability and relationship to quantitative social trait variation in rhesus monkeys

Molecular Autism(2021)10.1186/s13229-021-00442-w

N/A

0DataRank · unranked

14 citations

Catherine F. Talbot, Emanuela Argilli, Alyssa C. Maness, Sierra M. V. Simmons, Noreen Mohsin +6 more

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

Nature Communications(2022)10.1038/s41467-022-34264-y

N/A

0DataRank · unranked

45 citations

Christopher Schröder, Ilaria Parenti, Carine Dalle, Agnès Rastetter, Theresa Kühnel +32 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

De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a Range of Brain Malformations Without Skeletal Abnormalities

Pediatric Neurology(2022)10.1016/j.pediatrneurol.2022.03.005

N/A

0DataRank · unranked

0 citations

Emanuela Argilli, Elliott H. Sherr, Kenneth A. Myers, Lyna Siafa

Pediatric Neurology Research in the Twenty-First Century: Status, Challenges, and Future Directions Post–COVID-19

Pediatric Neurology(2020)10.1016/j.pediatrneurol.2020.08.012

N/A

0DataRank · unranked

11 citations

Gabrielle deVeber, Barry E. Kosofsky, Erika F. Augustine, Alexander G. Bassuk, Amy R. Brooks‐Kayal +18 more

The variant landscape and function of DDX3X in cancer and neurodevelopmental disorders

Trends in Molecular Medicine(2023)10.1016/j.molmed.2023.06.003

N/A

0DataRank · unranked

43 citations

Elliott H. Sherr, Stephen N. Floor, Margaret Gadek

Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis

Journal of Medical Genetics(2023)10.1136/jmg-2023-109293

N/A

0DataRank · unranked

3 citations

Emanuela Argilli, Stéphanie Valence, Lucile Boutaud, Nathalie Le Roux, Cyril Mignot +17 more

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595

N/A

0DataRank · unranked

1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008

N/A

0DataRank · unranked

24 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Discovering the gene-brain-behavior link in autism via generative machine learning

Science Advances(2024)10.1126/sciadv.adl5307

N/A

0DataRank · unranked

16 citations

Haris I. Sair, Elliott H. Sherr, Pratik Mukherjee, Gustavo K. Rohde, Shinjini Kundu

Vasopressin deficiency: a hypothesized driver of both social impairment and fluid imbalance in autism spectrum disorder

Molecular Psychiatry(2024)10.1038/s41380-024-02497-6

N/A

0DataRank · unranked

5 citations

Neil Gesundheit, Elliott H. Sherr, Antonio Y. Hardan, Karen J. Parker, Lauren Clarke

Noise induces Ca2+ signaling waves and Chop/S-Xbp1 expression in the hearing cochlea

JCI Insight(2024)10.1172/jci.insight.181783

N/A

0DataRank · unranked

4 citations

Jiang Li, Noura Ismail Mohamad, Ian R. Matthews, P. K. Santra, Elliott H. Sherr +2 more

Basic helix-loop-helix transcription factor BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalities

medRxiv(2024)10.1101/2024.10.11.24312856

N/A

0DataRank · unranked

2 citations

Emanuela Argilli, Elizabeth George, Tuğba Kalaycı, Zehra Oya Uyguner, Birsen Karaman +21 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

Missense ABI2 variants linked to a neurodevelopmental disorder with intellectual disability, epilepsy, hypoplasia of the corpus callosum, and white matter abnormalities

medRxiv(2025)10.1101/2025.05.19.25327541

N/A

0DataRank · unranked

1 citations

Caleb Yang, Carolyn Le, Amanda M. Elashoff, Kendall C. Parks, Clare Bakker +18 more

Overcoming presynaptic effects of VAMP2 mutations with 4‐aminopyridine treatment

Human Mutation(2020)10.1002/humu.24109

N/A

0DataRank · unranked

21 citations

Haiyan Li, Barış Alten, Magda Santos, Ruiji Jiang, Brianna M. Paul +15 more