Christian R. Marshall

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 6%percentile

0.208Author DataRank

Indexed papers

2in 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 2 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.

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031

Top 65%

0.208DataRank

Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Papers

Driven by 21 papers — median percentile 35. Top paper: “Genomic architecture of autism from comprehensive whole-genome sequence annotation”.

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Cell(2022)10.1016/j.cell.2022.10.009

N/A

4.6DataRank · unranked

285 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus

Journal of Medical Genetics(2013)10.1136/jmedgenet-2013-102064

N/A

1.4DataRank · unranked

38 citations

Yi-Hsiang Hsu, Unnur Styrkarsdottir, Bert H Eussen, Annelies de Klein, Marjolein J. Peters +81 more

Functional impact of global rare copy number variation in autism spectrum disorders

Nature(2010)10.1038/nature09146

N/A

1.1DataRank · unranked

2044 citations

Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan +204 more

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

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

Mild Idiopathic Infantile Hypercalcemia—Part 1: Biochemical and Genetic Findings

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab431

N/A

0.840DataRank · unranked

20 citations

Edwin J. Young, Michelle Furman, Yesmino Elia, Esther Assor, David Chitayat +11 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

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

0.757DataRank · unranked

154 citations

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

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

N/A

0.738DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Common Genetic Variation and Age of Onset of Anorexia Nervosa

Biological Psychiatry Global Open Science(2021)10.1016/j.bpsgos.2021.09.001

N/A

0.726DataRank · unranked

30 citations

Laura M. Thornton, Zeynep Yılmaz, Jessica H. Baker, Jonathan R. I. Coleman, Roger A.H. Adan +95 more

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

UNC Libraries(2020)10.17615/hmn0-qq55

N/A

0.483DataRank · unranked

24 citations

Dandan Cao, Irene Drmic, Yong‐hui Jiang, Christian R. Marshall, Jun Luo +27 more

Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variants

European Journal of Human Genetics(2021)10.1038/s41431-021-00821-0

N/A

0.416DataRank · unranked

15 citations

Marie Shaw, Cyril Mignot, Delphine Héron, Sandra Chantot‐Bastaraud, Cecile Cieuta Walti +51 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

0.345DataRank · unranked

9 citations

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

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031

Top 65%

0.208DataRank

Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function

Nature Genetics(2025)10.1038/s41588-025-02361-5

N/A

0.208DataRank · unranked

3 citations

Aisha Ahmad, Paranchai Boonsawat, Jasmine Shahanoor Hinzen, Mareike Lohse, Boris Bouazza‐Arostegui +95 more

Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of MUC5B

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202106-1456oc

N/A

0DataRank · unranked

30 citations

Zhen Liu, Vito Mennella, Giorgia Radicioni, Adrienn N. Goczi, Alexandra Albulescu +14 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

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111

N/A

0DataRank · unranked

0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 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

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y

N/A

0DataRank · unranked

12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more

Christian R. Marshall

Indexed papers

Top data-sharing exemplar

Papers