Sébastien Jacquemont

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 2%percentile

1.9Author 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.

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs

Human Brain Mapping(2021)10.1002/hbm.25354

Top 18%

1.2DataRank

Top 18%73 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E. Villalón‐Reina +95 more

Papers

Driven by 44 papers — median percentile 57. Top paper: “Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs”.

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs

Human Brain Mapping(2021)10.1002/hbm.25354

Top 18%

1.2DataRank

Top 18%73 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E. Villalón‐Reina +95 more

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

Nature(2012)10.1038/nature11091

N/A

0.911DataRank · unranked

434 citations

Jason Willer, Michael E. Talkowski, Edwin C. Oh, Yu Taniguchi, Sébastien Jacquemont +10 more

Phenotypic effects of genetic variants associated with autism

Nature Medicine(2023)10.1038/s41591-023-02408-2

N/A

0.663DataRank · unranked

82 citations

Freddy Cliquet, Richard Anney, Clara Moreau, Nicolas Traut, Alexandre Mathieu +20 more

Protein synthesis levels are increased in a subset of individuals with fragile X syndrome

Human Molecular Genetics(2018)10.1093/hmg/ddy099

N/A

0.646DataRank · unranked

73 citations

Laura Pacini, Aia E Jønch, Giulia Cencelli, Izabela Rozenberg, Yunsheng He +10 more

Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

Nature Human Behaviour(2023)10.1038/s41562-023-01541-9

N/A

0.588DataRank · unranked

28 citations

Kuldeep Kumar, Karin Saltoun, Claudia Modenato, Clara Moreau, Sandra Martin‐Brevet +27 more

Thalamocortical organoids enable in vitro modeling of 22q11.2 microdeletion associated with neuropsychiatric disorders

Cell stem cell(2024)10.1016/j.stem.2024.01.010

N/A

0.571DataRank · unranked

44 citations

Chang N. Kim, Jayden Ross, Kelsey M. Hennick, Sih‐Rong Wu, Neha Paranjape +22 more

Genetic and phenotypic similarity across major psychiatric disorders: a systematic review and quantitative assessment

Translational Psychiatry(2024)10.1038/s41398-024-02866-3

N/A

0.561DataRank · unranked

41 citations

Cécile Poulain, Catherine Proulx, Clara Moreau, Ridha Joober, Baudouin Forgeot d’Arc +3 more

Stability of polygenic scores across discovery genome-wide association studies

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100091

N/A

0.550DataRank · unranked

38 citations

Alison Merikangas, Kosha Ruparel, Sébastien Jacquemont, David C. Glahn, Raquel E. Gur +3 more

Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions

Brain(2022)10.1093/brain/awac315

N/A

0.483DataRank · unranked

24 citations

Kuldeep Kumar, Annabelle Harvey, Guillaume Huguet, Sebastian Urchs, Laura M. Schultz +21 more

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA Working Groups on CNVs

PsyArXiv (OSF Preprints)(2021)10.31234/osf.io/57erc

Top 43%

0.437DataRank

Top 43%12 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Julio E. Villalón‐Reina, Ingrid Agartz +95 more

Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age

Advanced Genetics(2022)10.1002/ggn2.202200012

Top 57%

0.281DataRank

Top 57%4 citations

Élise Douard, Robin L. Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan +10 more

Gathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research

Genes(2023)10.3390/genes14010169

N/A

0.269DataRank · unranked

5 citations

T. Blaine Crowley, Brenda Finucane, Emily McClellan, Sarah Donoghue, Sixto García‐Miñáur +10 more

Sub-diagnostic effects of genetic variants associated with autism

medRxiv(2021)10.1101/2021.02.12.21251621

N/A

0.179DataRank · unranked

2 citations

Freddy Cliquet, Richard Anney, Clara Moreau, Nicolas Traut, Alexandre Mathieu +20 more

Copy-number variants in the contactin-5 gene are a potential risk factor for autism spectrum disorder

Research in autism spectrum disorders(2022)10.1016/j.rasd.2022.102055

N/A

0DataRank · unranked

3 citations

Guillaume Huguet, Qin He, Amélie Musa-Johnson, Élise Douard, Mor Absa Loum +18 more

Spliceosome malfunction causes neurodevelopmental disorders with overlapping features

Journal of Clinical Investigation(2023)10.1172/jci171235

N/A

0DataRank · unranked

44 citations

Qin Wang, Allan Bayat, Mark R. Battig, Yijing Zhou, Daniëlle G.M. Bosch +95 more

Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants

American Journal of Psychiatry(2023)10.1176/appi.ajp.20220304

N/A

0DataRank · unranked

26 citations

Claudia Modenato, Clara Moreau, Christopher R. K. Ching, Annabelle Harvey, Sandra Martin‐Brevet +35 more

Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers

Biological Psychiatry(2023)10.1016/j.biopsych.2023.08.018

N/A

0DataRank · unranked

6 citations

Tobias Kaufmann, Dennis van der Meer, Oleksandr Frei, Ingrid Agartz, David Ames +95 more

Using rare genetic mutations to revisit structural brain asymmetry

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.17.537199

N/A

0DataRank · unranked

4 citations

Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara Moreau +25 more

Subcortical brain alterations in carriers of genomic copy number variants

medRxiv(2023)10.1101/2023.02.14.23285913

N/A

0DataRank · unranked

2 citations

Claudia Modenato, Clara Moreau, Christopher R. K. Ching, Annabelle Harvey, Sandra Martin‐Brevet +36 more

Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability

medRxiv(2023)10.1101/2023.11.29.23299190

N/A

0DataRank · unranked

0 citations

Vincent-Raphaël Bourque, Élise Douard, Guillaume Huguet, Cécile Poulain, Jay P. Ross +19 more

Challenges in Multi-Task Learning for fMRI-Based Diagnosis: Benefits for Psychiatric Conditions and CNVs Would Likely Require Thousands of Patients

PsyArXiv (OSF Preprints)(2023)10.31234/osf.io/srmx7

N/A

0DataRank · unranked

0 citations

Clara Moreau, Kuldeep Kumar, Guillaumeaf, Sebastian Urchs, Hanad Sharmarke +17 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

Using rare genetic mutations to revisit structural brain asymmetry

Nature Communications(2024)10.1038/s41467-024-46784-w

N/A

0DataRank · unranked

8 citations

Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara Moreau +25 more

Challenges in multi-task learning for fMRI-based diagnosis: Benefits for psychiatric conditions and CNVs would likely require thousands of patients

Imaging Neuroscience(2024)10.1162/imag_a_00222

N/A

0DataRank · unranked

3 citations

Clara Moreau, Kuldeep Kumar, Guillaume Huguet, Sebastian Urchs, Hanad Sharmarke +17 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

Copy number variants and the tangential expansion of the cerebral cortex

Nature Communications(2025)10.1038/s41467-025-56855-1

N/A

0DataRank · unranked

3 citations

Kuldeep Kumar, Jakub Kopál, Guillaume Huguet, Zohra Saci, Martineau Jean‐Louis +6 more

A pattern-learning algorithm associates copy number variations with brain structure and behavioural variables in an adolescent population cohort

Nature Biomedical Engineering(2025)10.1038/s41551-025-01454-0

N/A

0DataRank · unranked

1 citations

Guillaume Huguet, Justin Marotta, Shambhavi Aggarwal, Nicole Osayande, Kuldeep Kumar +11 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

Cortical differences across psychiatric disorders and associated common and rare genetic variants

medRxiv(2025)10.1101/2025.04.16.25325971

N/A

0DataRank · unranked

2 citations

Zhijie Liao, Jakub Kopál, Clara Moreau, Christopher R. K. Ching, Claudia Modenato +30 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

Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2025)10.1016/j.bpsc.2025.05.010

N/A

0DataRank · unranked

1 citations

Ida E. Sønderby, George Kirov, Abdel Abdellaoui, Ingrid Agartz, David Ames +95 more

Insufficient Evidence for “Autism-Specific” Genes

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.004

N/A

0DataRank · unranked

169 citations

Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +8 more

Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia

Nature Communications(2020)10.1038/s41467-020-18997-2

N/A

0DataRank · unranked

67 citations

Sebastian Urchs, Kuldeep Kumar, Pierre Orban, Catherine Schramm, Guillaume Dumas +17 more

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

medRxiv(2020)10.1101/2020.01.14.20017426

N/A

0DataRank · unranked

14 citations

Joanne Doherty, Richard Anney, Kevin M. Antshel, Carrie E. Bearden, Raphael Bernier +26 more

Effects-sizes of deletions and duplications on autism risk across the genome

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.09.979815

N/A

0DataRank · unranked

5 citations

Abderrahim Zeribi, Catherine Schramm, Petra Tamer, Mor Absa Loum, Sabrina Nowak +19 more

Genome wide analysis of gene dosage in 24,092 individuals shows that 10,000 genes modulate cognitive ability

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.03.024554

N/A

0DataRank · unranked

3 citations

Catherine Schramm, Élise Douard, Tamer Petra, Antoine Main, Pauline Monin +34 more

Neuropsychiatric copy number variants exert shared effects on human brain structure

medRxiv(2020)10.1101/2020.04.15.20056531

N/A

0DataRank · unranked

3 citations

Kuldeep Kumar, Clara Moreau, Sandra Martin‐Brevet, Guillaume Huguet, Catherine Schramm +27 more

Insufficient Evidence for “Autism-Specific” Genes

OSF Preprints (OSF Preprints)(2020)10.31219/osf.io/24gm3

N/A

0DataRank · unranked

3 citations

Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +8 more

Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability

Molecular Psychiatry(2021)10.1038/s41380-020-00985-z

N/A

0DataRank · unranked

67 citations

Catherine Schramm, Élise Douard, Petra Tamer, Antoine Main, Pauline Monin +34 more

Stability of Polygenic Scores Across Discovery Genome-Wide Association Studies

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.18.449060

N/A

0DataRank · unranked

14 citations

Alison Merikangas, Kosha Ruparel, Sébastien Jacquemont, David C. Glahn, Raquel E. Gur +3 more

Copy-Number Variants in The Contactin-5 Gene Are a Potential Risk Factor for Autism Spectrum Disorder

Research Square(2021)10.21203/rs.3.rs-660740/v1

N/A

0DataRank · unranked

0 citations

Guillaume Huguet, Qin He, Amélie Musa-Johnson, Élise Douard, Mor Absa Loum +16 more

Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry

Biological Psychiatry(2022)10.1016/j.biopsych.2022.08.024

N/A

0DataRank · unranked

28 citations

Annabelle Harvey, Kuldeep Kumar, Guillaume Huguet, Sebastian Urchs, Élise Douard +24 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

Sébastien Jacquemont

Indexed papers

Top data-sharing exemplar

Papers