Stephen W. Scherer

ORCID: 0000-0002-8326-1999

Also affiliated with Hospital for Sick Children, SickKids Foundation

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 4%percentile

0.579Author 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.

Structural variation in the human genome

Nature Reviews Genetics(2006)10.1038/nrg1767

Top 18%

1.1DataRank

Top 18%2077 citations

Andrew R. Carson, Stephen W. Scherer, Lars Feuk

Papers

Driven by 31 papers — median percentile 66. Top paper: “Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications”.

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

Brain(2021)10.1093/brain/awab321

N/A

2.9DataRank · unranked

149 citations

Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert +95 more

Structural variation in the human genome

Nature Reviews Genetics(2006)10.1038/nrg1767

Top 18%

1.1DataRank

Top 18%2077 citations

Andrew R. Carson, Stephen W. Scherer, Lars Feuk

Structural Variation of Chromosomes in Autism Spectrum Disorder

The American Journal of Human Genetics(2008)10.1016/j.ajhg.2007.12.009

N/A

1.1DataRank · unranked

1855 citations

Abdul Noor, John B. Vincent, Anath C. Lionel, Lars Feuk, Jennifer Skaug +30 more

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Cell Genomics(2023)10.1016/j.xgen.2023.100356

N/A

1.0DataRank · unranked

43 citations

Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris +95 more

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Biological Psychiatry(2021)10.1016/j.biopsych.2021.05.029

N/A

0.828DataRank · unranked

249 citations

Jooeun Kang, Adrián I. Campos, Jonathan R. I. Coleman, Alexis C. Edwards, Hanga Galfalvy +95 more

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology

European Journal of Human Genetics(2023)10.1038/s41431-023-01445-2

Top 34%

0.579DataRank

Top 34%20 citations

Elia Marcos-Grañeda, Linnea A. Weiss, Christina A. Gurnett, Anne Marie Jelsig, Susanne H. Vineke +50 more

Chromosome X-wide common variant association study in autism spectrum disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.008

N/A

0.533DataRank · unranked

34 citations

D. Chen, Worrawat Engchuan, Thiago Peixoto Leal, Bhooma Thiruvahindrapuram, Brett Trost +15 more

Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder

medRxiv(2024)10.1101/2024.07.18.24310640

N/A

0.208DataRank · unranked

3 citations

D. Chen, Worrawat Engchuan, Thiago Peixoto Leal, Bhooma Thiruvahindrapuram, Brett Trost +15 more

DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes

European Journal of Human Genetics(2022)10.1038/s41431-022-01083-0

N/A

0DataRank · unranked

28 citations

Eric Chater‐Diehl, Sanaa Choufani, Elizabeth Y Wei, Rebecca R. Kianmahd, Anna Yu +8 more

Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency

Human Mutation(2022)10.1002/humu.24332

N/A

0DataRank · unranked

16 citations

Tianyun Wang, Madelyn A. Gillentine, Tiana M. Scott, Aliska M. Berry, Mahshid S. Azamian +19 more

Rare copy number variation in posttraumatic stress disorder

Molecular Psychiatry(2022)10.1038/s41380-022-01776-4

N/A

0DataRank · unranked

6 citations

Worrawat Engchuan, Guillaume Huguet, Marieke Klein, Jeffrey R. MacDonald, Omar Shanta +87 more

Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors

medRxiv(2022)10.1101/2022.07.03.22277199

N/A

0DataRank · unranked

9 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

CUX1-related neurodevelopmental disorder: Deep insights into phenotype-genotype spectrum and underlying pathology

Research Square(2022)10.21203/rs.3.rs-2401638/v1

Top 100%

0DataRank

Top 100%0 citations

Elia Marcos-Grañeda, Linnea A. Weiss, Christina A. Gurnett, Anne Marie Jelsig, Susanne H. Vineke +46 more

GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors

American Journal of Psychiatry(2023)10.1176/appi.ajp.21121266

N/A

0DataRank · unranked

150 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia

UNC Libraries(2020)10.17615/7vzp-r892

N/A

0DataRank · unranked

0 citations

Tracy Stockley, Tara Paton, Stephen W. Scherer, Sharon Dell, David A. Hall +7 more

FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1373

N/A

0DataRank · unranked

13 citations

Arianna Ricciardello, Laura Turriziani, Giorgia Calabrese, Marilena Briguglio, Maria Boncoddo +17 more

The Phenotypic variability of 16p11.2 distal BP2–BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples

Journal of Medical Genetics(2023)10.1136/jmg-2022-108818

N/A

0DataRank · unranked

4 citations

Lia D’Abate, Dimitri J. Stavropoulos, Jennifer Howe, Irene Drmic, Ny Hoang +6 more

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63130

N/A

0DataRank · unranked

3 citations

Soumya Rao, Sandra von Hardenberg, Dong Li, Liza L. Cox, Paul C. Lee +34 more

Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus

medRxiv(2023)10.1101/2023.12.21.23300383

N/A

0DataRank · unranked

4 citations

Clarrisa A. Bradley, Jennifer Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum +22 more

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.003

N/A

0DataRank · unranked

10 citations

Clarrisa A. Bradley, Jennifer Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum +29 more

Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes

Cell Genomics(2024)10.1016/j.xgen.2024.100721

N/A

0DataRank · unranked

6 citations

Thomas Renné, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, Sayeh Kazem +25 more

Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.16.589618

N/A

0DataRank · unranked

3 citations

Thomas Renne, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, Sayeh Kazem +25 more

Rare variants in BMAL1 are associated with a neurodevelopmental syndrome

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2427085122

N/A

0DataRank · unranked

3 citations

Dechun Chen, Bumsik Cho, Rebecca S. Moore, Mohnish Suri, Hana Safraou +11 more

Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia

Brain(2025)10.1093/brain/awaf273

N/A

0DataRank · unranked

1 citations

Ny Hoang, Jamie C Stark, Sunny Cui, Emanuela Pannia, Chung Ting Tsoi +36 more

Determinants of functional burden pleiotropy and gene dosage responses across human traits

medRxiv(2025)10.1101/2025.02.25.25322833

N/A

0DataRank · unranked

3 citations

Kuldeep Kumar, Guillaume Huguet, Florian Benitiere, Josephine Mollon, Thomas Renne +12 more

Determinants of pleiotropy and monotonic gene dosage responses across human traits

Research Square(2025)10.21203/rs.3.rs-7547111/v1

N/A

0DataRank · unranked

0 citations

Kuldeep Kumar, Guillaume Huguet, Josephine Mollon, Thomas Renne, Laura M. Schultz +13 more

Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex

Research Square(2025)10.21203/rs.3.rs-8099338/v1

N/A

0DataRank · unranked

0 citations

Sayeh Kazem, Guillaume Huguet, Worrawat Engchuan, Jakub Kopál, Thomas Renne +22 more

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

medRxiv(2020)10.1101/2020.12.18.20248226

N/A

0DataRank · unranked

10 citations

Guillaume Butler‐Laporte, Ning Shang, Chen Weng, Atlas Khan, Manal Alaamery +44 more

RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes

Molecular Psychiatry(2021)10.1038/s41380-021-01035-y

N/A

0DataRank · unranked

16 citations

Richard S. Smith, Lance H. Rodan, Mark Gorman, Margaret A. Hojlo, Emily A. Garvey +25 more

Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

medRxiv(2020)10.1101/2020.12.01.20241281

N/A

0DataRank · unranked

29 citations

Jooeun Kang, Adrián I. Campos, Jonathan R. I. Coleman, Alexis C. Edwards, Hanga Galfalvy +95 more

Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

medRxiv(2021)10.1101/2021.03.22.21253711

N/A

0DataRank · unranked

5 citations

Yuanyuan Liu, Cathrine E. Gjerulfsen, Mahmoud Koko, Lukas Sonnenberg, Julian Schubert +95 more

Stephen W. Scherer

Indexed papers

Top data-sharing exemplar

Papers