David M. Hougaard

Also affiliated with Stellenbosch University, University Medical Center Utrecht, University of California San Diego, MSB Medical School Berlin, Lundbeck Foundation, Human Longevity (United States), Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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

2.9Author 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.

Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals

Nature Medicine(2023)10.1038/s41591-023-02653-5

Top 10%

2.1DataRank

Top 10%181 citations

Rachel L. Kember, Joseph D. Deak, Heng Xu, Sylvanus Toikumo, Kai Yuan +44 more

Papers

Driven by 51 papers — median percentile 83. Top paper: “Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism”.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Cell(2020)10.1016/j.cell.2019.12.036

N/A

9.5DataRank · unranked

2470 citations

Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An +95 more

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Nature Genetics(2023)10.1038/s41588-022-01285-8

N/A

6.1DataRank · unranked

775 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen +81 more

A large-scale genome-wide association study meta-analysis of cannabis use disorder

The Lancet Psychiatry(2020)10.1016/s2215-0366(20)30339-4

N/A

5.5DataRank · unranked

384 citations

Ditte Demontis, Thorgeir E. Thorgeirsson, Raymond K. Walters, Renato Polimanti, Alexander S. Hatoum +91 more

Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

Nature Medicine(2023)10.1038/s41591-023-02352-1

N/A

3.6DataRank · unranked

313 citations

Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko +38 more

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0

N/A

2.8DataRank · unranked

151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 more

The genetic architecture of sporadic and multiple consecutive miscarriage

Nature Communications(2020)10.1038/s41467-020-19742-5

N/A

2.6DataRank · unranked

122 citations

Ana Gonçalves Soares, Teresa Ferreira, Jodie N. Painter, Jenny C. Censin, Samantha Laber +50 more

Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals

Nature Medicine(2023)10.1038/s41591-023-02653-5

Top 10%

2.1DataRank

Top 10%181 citations

Rachel L. Kember, Joseph D. Deak, Heng Xu, Sylvanus Toikumo, Kai Yuan +44 more

Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups

Nature Genetics(2022)10.1038/s41588-022-01171-3

N/A

1.7DataRank · unranked

76 citations

Jakob Grove, Thomas D. Als, Joanna Martin, Georgios Voloudakis, Sandra Meier +29 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

medRxiv(2022)10.1101/2022.02.14.22270780

N/A

1.5DataRank · unranked

63 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Leila Farajzadeh +42 more

Biological insights from 108 schizophrenia-associated genetic loci

Nature(2014)10.1038/nature13595

N/A

1.3DataRank · unranked

8042 citations

Stephan Ripke, Aiden Corvin, Jesse R. Dixon, Kai-How Farh, Peter Holmans +284 more

Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications

Nature Genetics(2023)10.1038/s41588-023-01563-z

N/A

1.3DataRank · unranked

120 citations

Marco Galimberti, Joseph D. Deak, Frank R. Wendt, Arjun Bhattacharya, Dóra Koller +26 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

Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity

Scientific Reports(2023)10.1038/s41598-022-26845-0

N/A

0.970DataRank · unranked

30 citations

Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove +48 more

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature Genetics(2022)10.1038/s41588-022-01104-0

N/A

0.969DataRank · unranked

638 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +112 more

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Nature Genetics(2017)10.1038/ng.3863

N/A

0.950DataRank · unranked

562 citations

Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki +18 more

Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth

PLoS Genetics(2020)10.1371/journal.pgen.1009163

N/A

0.841DataRank · unranked

18 citations

Ron Nudel, Michael E. Benros, Kristin Skogstrand, Simon Fishilevich, iPSYCH-BROAD +10 more

Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study

The Lancet Psychiatry(2023)10.1016/s2215-0366(23)00004-4

Top 24%

0.832DataRank

Top 24%34 citations

Simone Montalbano, Morteza Vaez, Morten Dybdahl Krebs, Jonas Byberg-Grauholm, Preben Bo Mortensen +12 more

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature Genetics(2017)10.1038/ng.3903

N/A

0.826DataRank · unranked

246 citations

David M. Hougaard, Mandy Johnstone, Nicholas Bass, Jaana Suvisaari, Minna Torniainen +21 more

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature Neuroscience(2019)10.1038/s41593-019-0527-8

N/A

0.815DataRank · unranked

228 citations

F. Kyle Satterstrom, Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis +17 more

Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder

Nature Genetics(2024)10.1038/s41588-024-01707-9

N/A

0.785DataRank · unranked

186 citations

Adam X. Maihofer, Elizabeth G. Atkinson, Chia‐Yen Chen, Karmel W. Choi, Jonathan R. I. Coleman +95 more

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

The American Journal of Human Genetics(2018)10.1016/j.ajhg.2018.05.002

N/A

0.713DataRank · unranked

115 citations

F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse +45 more

Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities

medRxiv(2022)10.1101/2022.08.24.22279149

N/A

0.648DataRank · unranked

12 citations

Mitja Kurki, Jakob Grove, Georgios Voloudakis, Karen Therrien, Elisa Tasanko +38 more

Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information

Biological Psychiatry(2021)10.1016/j.biopsych.2021.09.020

N/A

0.639DataRank · unranked

70 citations

Karmel W. Choi, Jonathan R. I. Coleman, Nikolaos P. Daskalakis, Christy A. Denckla, Elizabeth Ketema +95 more

Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes

Brain(2021)10.1093/brain/awab260

N/A

0.626DataRank · unranked

64 citations

João Fadista, Jonas Bybjerg‐Grauholm, Vivek Appadurai, Michael S. Hildebrand, Thomas Folkmann Hansen +34 more

ADuLT: An efficient and robust time-to-event GWAS

Nature Communications(2023)10.1038/s41467-023-41210-z

N/A

0.571DataRank · unranked

44 citations

Esben Agerbo, Oleguer Plana‐Ripoll, Jette Steinbach, Morten Dybdahl Krebs, David M. Hougaard +11 more

The Relationship of Attention-Deficit/Hyperactivity Disorder With Posttraumatic Stress Disorder: A Two-Sample Mendelian Randomization and Population-Based Sibling Comparison Study

Biological Psychiatry(2022)10.1016/j.biopsych.2022.08.012

N/A

0.538DataRank · unranked

35 citations

Miguel Garcia‐Argibay, Brenda Cabrera‐Mendoza, Unnur Valdimarsdóttir, Joel Gelernter, Murray B Stein +91 more

Genome-wide association study of school grades identifies a genetic overlap between language ability, psychopathology and creativity

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.09.075226

N/A

0.524DataRank · unranked

13 citations

Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove +21 more

Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots

Nature Communications(2023)10.1038/s41467-023-36392-5

N/A

0.520DataRank · unranked

31 citations

Zhihong Zhu, Nis Borbye‐Lorenzen, Sanne Grundvad Boelt, Arieh S. Cohen, Kristin Skogstrand +16 more

Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.03.019

N/A

0.515DataRank · unranked

30 citations

Casper Pedersen, Morten Arendt Rasmussen, Ni Wang, Matteo Soverini, Amelie Fritz +29 more

Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder

Nature Genetics(2023)10.1038/s41588-023-01593-7

N/A

0.505DataRank · unranked

28 citations

Isabell Brikell, Dorte Helenius, Robert Loughnan, Joel Mefford, Clare E. Palmer +22 more

Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis

Frontiers in Genetics(2021)10.3389/fgene.2021.711624

N/A

0.434DataRank · unranked

17 citations

Jakob Grove, Sandra Meier, Marie Bækvad‐Hansen, Judith Becker Nissen, Thomas D. Als +11 more

ASD and ADHD have a similar burden of rare protein-truncating variants

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/277707

N/A

0.434DataRank · unranked

17 citations

Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis, Christine Stevens +18 more

Adolescent residential mobility, genetic liability and risk of schizophrenia, bipolar disorder and major depression

The British Journal of Psychiatry(2020)10.1192/bjp.2020.8

N/A

0.425DataRank · unranked

16 citations

Betina B. Trabjerg, Kathleen R. Merikangas, Ole Mors, Anders D. Børglum, David M. Hougaard +7 more

Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus

Neuro-Oncology(2023)10.1093/neuonc/noad042

N/A

0.406DataRank · unranked

14 citations

Shaobo Li, Adam Rosenbaum, Christian M. Hagen, Ulrik Kristoffer Stoltze, Sally Ljungqvist +13 more

A genome-wide association study on medulloblastoma

Journal of Neuro-Oncology(2020)10.1007/s11060-020-03424-9

N/A

0.396DataRank · unranked

13 citations

Anna M. Dahlin, Carl Wibom, Ulrika Andersson, Jonas Bybjerg‐Grauholm, Isabelle Deltour +23 more

The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders

Cell Genomics(2023)10.1016/j.xgen.2023.100457

N/A

0.385DataRank · unranked

12 citations

Zhihong Zhu, Esben Agerbo, Clara Albiñana, Michael E. Benros, Beilei Bian +19 more

Genome-wide association study identifies new loci associated with OCD

medRxiv(2024)10.1101/2024.03.06.24303776

N/A

0.330DataRank · unranked

8 citations

Matthew Halvorsen, Chao Tian, Christian Rück, Gerd Kvale, Bjarne Hansen +29 more

Genetic correlates of vitamin D-binding protein and 25 hydroxyvitamin D in neonatal dried blood spots

medRxiv(2022)10.1101/2022.06.08.22276164

N/A

0.292DataRank · unranked

6 citations

Zhihong Zhu, Nis Borbye‐Lorenzen, Sanne Grundvad Boelt, Arieh S. Cohen, Kristin Skogstrand +16 more

Polygenic profiles define aspects of clinical heterogeneity in ADHD

medRxiv(2021)10.1101/2021.07.13.21260299

N/A

0.269DataRank · unranked

5 citations

Isabell Brikell, Dorte Helenius, Robert Loughnan, Joel Mefford, Clare E. Palmer +22 more

Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology

npj Genomic Medicine(2024)10.1038/s41525-024-00450-8

N/A

0.241DataRank · unranked

4 citations

Morten Dybdahl Krebs, Anders Rosengren, Morteza Vaez, Kajsa-Lotta Georgii Hellberg, Preben Bo Mortensen +28 more

Genome-wide association study of febrile seizures identifies seven new loci implicating fever response and neuronal excitability genes

medRxiv(2020)10.1101/2020.11.18.20233916

N/A

0.208DataRank · unranked

3 citations

João Fadista, Jonas Bybjerg‐Grauholm, Vivek Appadurai, Michael S. Hildebrand, Thomas Folkmann Hansen +34 more

Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p

medRxiv(2022)10.1101/2022.03.23.22272826

N/A

0.192DataRank · unranked

2 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +15 more

Phenotypic and ancestry-related assortative mating in autism

Molecular Autism(2024)10.1186/s13229-024-00605-5

N/A

0.165DataRank · unranked

2 citations

J. Dylan Weissenkampen, Rachel L. Kember, David M. Hougaard, Jonas Bybjerg‐Grauholm, Thomas Werge +10 more

Bilirubin metabolism in early life and respiratory health during preschool age: A combined analysis of two independent birth cohorts

Med(2024)10.1016/j.medj.2024.07.021

N/A

0.122DataRank · unranked

1 citations

Nicklas Brustad, Anders Eliasen, Mina Ali, Tingting Wang, Morten Arendt Rasmussen +14 more

Polygenic profiles define aspects of clinical heterogeneity in ADHD

Research Square(2021)10.21203/rs.3.rs-702232/v1

N/A

0.117DataRank · unranked

1 citations

Sonja LaBianca, Isabell Brickell, Dorte Helenius, Robert Loughnan, Joel Mefford +22 more

Polygenic heterogeneity across obsessive-compulsive disorder subgroups defined by a comorbid diagnosis

medRxiv(2021)10.1101/2021.05.21.21257530

N/A

0.104DataRank · unranked

1 citations

Jakob Grove, Sandra Meier, Marie Bækvad‐Hansen, Judith Becker Nissen, Thomas D. Als +11 more

Disentangling the shared genetics of ADHD, cannabis use disorder and cannabis use and prediction of cannabis use disorder in ADHD

medRxiv(2024)10.1101/2024.02.22.24303124

N/A

0.104DataRank · unranked

1 citations

Jinjie Duan, Daniel Levey, G. Bragi Walters, Emma C. Johnson, Thorgeir E. Thorgeirsson +12 more

Associations of 25 Hydroxyvitamin D and High Sensitivity C-reactive Protein Levels in Early Life

Nutrients(2021)10.3390/nu14010015

N/A

0DataRank · unranked

13 citations

Nadia R. Fink, Jakob Stokholm, Klaus Bønnelykke, Nilofar V. Følsgaard, David M. Hougaard +5 more

The genetic and phenotypic correlates of neonatal Complement Component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders

medRxiv(2022)10.1101/2022.11.09.22281216

N/A

0DataRank · unranked

0 citations

Zhihong Zhu, Esben Agerbo, Clara Albiñana, Michael E. Benros, Beilei Bian +19 more

Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots

UNC Libraries(2024)10.17615/4537-h435

N/A

0DataRank · unranked

0 citations

Naomi R. Wray, Esben Agerbo, Preben Bo Mortensen, Nis Borbye‐Lorenzen, Thomas Werge +16 more

David M. Hougaard

Indexed papers

Top data-sharing exemplar

Papers