🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Dheeraj Malhotra

Roche (Switzerland)

ORCID: 0000-0003-4700-4407

Also affiliated with Biogen (United States)

Biochemistry, Genetics and Molecular BiologyNeuroscience

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
4.2Author 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 →

Top data-sharing exemplar

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

Frequency and Complexity of De Novo Structural Mutation in Autism

The American Journal of Human Genetics(2016)10.1016/j.ajhg.2016.02.018
Top 6%
3.6DataRank
Top 6%112 citations

Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R. Chapman +34 more

Papers

Driven by 18 papers — median percentile 80. Top paper: “Frequency and Complexity of De Novo Structural Mutation in Autism”.

Frequency and Complexity of De Novo Structural Mutation in Autism

The American Journal of Human Genetics(2016)10.1016/j.ajhg.2016.02.018
Top 6%
3.6DataRank
Top 6%112 citations

Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R. Chapman +34 more

Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility

Neuron(2022)10.1016/j.neuron.2021.12.034
N/A
3.4DataRank · unranked
101 citations

Eneritz Agirre, Mukund Kabbe, Cassandra A. van Tuijn, Abeer Heskol, Chao Zheng +12 more

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

Science(2008)10.1126/science.1155174
N/A
1.1DataRank · unranked
1822 citations

Anjene M Addington, Wellcome Trust Case Control Consortium, Anjené M. Addington, Sarah B. Pierce, Alex S. Nord +39 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725
N/A
1.1DataRank · unranked
1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 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

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

Cell(2012)10.1016/j.cell.2012.02.039
N/A
1.0DataRank · unranked
884 citations

Jonathan Sebat, Dheeraj Malhotra

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

Molecular Psychiatry(2011)10.1038/mp.2011.154
N/A
1.0DataRank · unranked
874 citations

A J Pocklington, D Ivanov, Samuel A. Rose, Andrew McQuillin, Hywel Williams +46 more

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474
N/A
0.990DataRank · unranked
733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders

Nature Neuroscience(2022)10.1038/s41593-022-01128-z
N/A
0.860DataRank · unranked
308 citations

Daniela Calini, Will Macnair, Lynette C. Foo, Eduard Urich, Ward Ortmann +11 more

Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression

Cell Reports(2020)10.1016/j.celrep.2020.108398
N/A
0.694DataRank · unranked
101 citations

Damon Polioudakis, Anna Yin, Vivek Swarup, Timothy S. Chang, Tam Nguyen +9 more

Analysis of the caudate nucleus transcriptome in individuals with schizophrenia highlights effects of antipsychotics and new risk genes

Nature Neuroscience(2022)10.1038/s41593-022-01182-7
N/A
0.648DataRank · unranked
74 citations

Qiang Chen, Andrew E. Jaffe, Joshua M. Stolz, Leonardo Collado‐Torres, Louise A. Huuki-Myers +32 more

Cross-disorder and disease-specific pathways in dementia revealed by single-cell genomics

Cell(2024)10.1016/j.cell.2024.08.019
N/A
0.584DataRank · unranked
48 citations

Yuyan Cheng, Lawrence Chen, Damon Polioudakis, Li‐Chun Lin, Vivianne Mitri +20 more

Disease-specific selective vulnerability and neuroimmune pathways in dementia revealed by single cell genomics

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.29.560245
Top 35%
0.567DataRank
Top 35%11 citations

Yuyan Cheng, Lawrence Chen, Damon Polioudakis, Li‐Chun Lin, Vivianne Mitri +18 more

Cell-type specific cis-eQTLs in eight brain cell-types identifies novel risk genes for human brain disorders

10.1101/2021.10.09.21264604
N/A
0.505DataRank · unranked
12 citations

Daniela Calini, Will Macnair, Lynette Foo, Eduard Urich, Ward Ortmann +11 more

A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluid

Cell Reports Methods(2023)10.1016/j.crmeth.2023.100533
N/A
0.416DataRank · unranked
15 citations

Tina Roostaei, Daniela Calini, Claudiu Diaconu, Samantha Epstein, Catarina Raposo +11 more

Single-nucleus and spatial transcriptomic profiling of human temporal cortex and white matter reveals key associations with AD pathology

Nature Communications(2025)10.1038/s41467-025-65350-6
N/A
0.345DataRank · unranked
9 citations

Julien Bryois, Daniela Calini, Lynette C. Foo, Jeroen J.M. Hoozemans, Archana Yadav +3 more

Microduplications of 16p11.2 are associated with schizophrenia

UNC Libraries(2020)10.17615/zwts-m549
N/A
0DataRank · unranked
0 citations

Jaya Ganesh, Detelina Grozeva, Vladimir Makarov, Abhishek Bhandari, Ravinesh A. Kumar +27 more

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

UNC Libraries(2020)10.17615/8m0s-na92
N/A
0DataRank · unranked
0 citations

John A. McGrath, Pamela Sklar, Gerald Nestadt, David J. Cutler, Paula Wolyniec +25 more