Anders D. Børglum

Also affiliated with Lundbeck Foundation

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 1%percentile

41.8Author DataRank

Indexed papers

12in 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 12 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.

Initial sequencing and comparative analysis of the mouse genome

Nature(2002)10.1038/nature01262

Top 1%

12.6DataRank

Top 1%7282 citations

Robert H. Waterston, Kerstin Lindblad‐Toh, Julien Lagarde, Josep F. Abril, PANKAJ AGARWAL +189 more

Papers

Driven by 109 papers — median percentile 90. Top paper: “Initial sequencing and comparative analysis of the mouse genome”.

Initial sequencing and comparative analysis of the mouse genome

Nature(2002)10.1038/nature01262

Top 1%

12.6DataRank

Top 1%7282 citations

Robert H. Waterston, Kerstin Lindblad‐Toh, Julien Lagarde, Josep F. Abril, PANKAJ AGARWAL +189 more

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 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

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Association between Mental Disorders and Subsequent Medical Conditions

New England Journal of Medicine(2020)10.1056/nejmoa1915784

N/A

6.2DataRank · unranked

483 citations

Oleguer Plana‐Ripoll, Esben Agerbo, Michael E. Benros, Anders D. Børglum, Maria Klitgaard Christensen +33 more

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

Nature Neuroscience(2020)10.1038/s41593-020-0643-5

N/A

6.1DataRank · unranked

406 citations

Julia Sealock, Sandra Sanchez-Roige, Toni-Kim Clarke, Daniel F. Levey, Zhongshan Cheng +21 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

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 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

Replication and meta-analysis of TMEM132D gene variants in panic disorder

Translational Psychiatry(2012)10.1038/tp.2012.85

N/A

2.8DataRank · unranked

97 citations

N Akula, J Schumacher, D Czamara, N Karbalai, Inez Myin‐Germeys +52 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

Shared genetic background between children and adults with attention deficit/hyperactivity disorder

Neuropsychopharmacology(2020)10.1038/s41386-020-0664-5

N/A

1.9DataRank · unranked

108 citations

Ditte Demontis, Cristina Sánchez‐Mora, Tetyana Zayats, Marieke Klein, Nina Roth Mota +49 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

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Genome Research(2010)10.1101/gr.107524.110

N/A

1.5DataRank · unranked

29661 citations

Matthew Hanna, Iain Mathieson, Sachet A. Shukla, Kristian Cibulskis, Andrew Kernytsky +8 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

Haploview: analysis and visualization of LD and haplotype maps

Bioinformatics(2004)10.1093/bioinformatics/bth457

N/A

1.4DataRank · unranked

14680 citations

B. Fry, Steve McCarroll, Jeffrey C. Barrett, Ben Fry, Duncan S. Palmer +2 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 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

Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell

Nature Medicine(1997)10.1038/nm0797-730

N/A

1.3DataRank · unranked

6916 citations

Anders D. Børglum, Dominique Bonnet

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

Partitioning heritability by functional annotation using genome-wide association summary statistics

Nature Genetics(2015)10.1038/ng.3404

N/A

1.2DataRank · unranked

3020 citations

Hilary K. Finucane, Anders D. Børglum, The RACI Consortium, Brendan K Bulik-Sullivan, Alexander Gusev +22 more

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Nature(2011)10.1038/nature10251

N/A

1.2DataRank · unranked

2729 citations

Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos +241 more

Schizophrenia risk from complex variation of complement component 4

Nature(2016)10.1038/nature16549

N/A

1.2DataRank · unranked

2481 citations

Nick Patterson, Heather de Rivera, Avery Davis, Timothy R. Hammond, Nolan Kamitaki +15 more

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Molecular Psychiatry(2022)10.1038/s41380-022-01793-3

N/A

1.1DataRank · unranked

66 citations

Emil Uffelmann, Benjamin Williams, Lucía Colodro‐Conde, Éloi Gagnon, Travis T. Mallard +95 more

Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature(2008)10.1038/nature07239

N/A

1.1DataRank · unranked

1503 citations

Michael C O'Donovan, Catherine H. Wilson, Manfred Kayser, Pentti J. Tienari, Aiden Corvin +72 more

Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease

Nature Cardiovascular Research(2024)10.1038/s44161-024-00488-y

N/A

1.1DataRank · unranked

48 citations

Joëlle A. Pasman, Ziyan Ma, Arvid Harder, Shuyang Yao, Nadine Parker +21 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/561472

N/A

0.977DataRank · unranked

17 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric Vallabh Minikel, Konrad J. Karczewski +35 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

Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis

Nature Genetics(2022)10.1038/s41588-022-01057-4

N/A

0.868DataRank · unranked

326 citations

Travis T. Mallard, Wonuola A. Akingbuwa, Hill F. Ip, Mark J. Adams, Cathryn M. Lewis +17 more

International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

Nature Communications(2015)10.1038/ncomms9019

N/A

0.860DataRank · unranked

309 citations

Younghun Han, George F. Mells, Yafang Li, Gideon M. Hirschfield, Casey S. Greene +518 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

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

pIRS: Profile-based Illumina pair-end reads simulator

Bioinformatics(2012)10.1093/bioinformatics/bts187

N/A

0.801DataRank · unranked

207 citations

Jianying Yuan, Yujian Shi, Jianliang Lu, Anders D. Børglum, Claire Churchhouse +9 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 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

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

Mapping the genetic landscape across 14 psychiatric disorders

Nature(2025)10.1038/s41586-025-09820-3

N/A

0.750DataRank · unranked

75 citations

Josefin Werme, Wouter J. Peyrot, Oleksandr Frei, Christiaan de Leeuw, Lucy Bicks +95 more

Transcript expression-aware annotation improves rare variant discovery and interpretation

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/554444

N/A

0.746DataRank · unranked

20 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +14 more

Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci

Molecular Psychiatry(2022)10.1038/s41380-022-01709-1

N/A

0.742DataRank · unranked

140 citations

Hang Zhou, Marco Galimberti, Daniel F. Levey, Frank R. Wendt, Sandra Sanchez-Roige +15 more

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2202764119

N/A

0.738DataRank · unranked

136 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +90 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

Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum

Biological Psychiatry(2021)10.1016/j.biopsych.2020.12.028

N/A

0.700DataRank · unranked

105 citations

Hanrui Wu, Phil H. Lee, Fotis Tsetsos, Lea K. Davis, Dongmei Yu +20 more

Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons

Nature Communications(2020)10.1038/s41467-020-19319-2

N/A

0.688DataRank · unranked

97 citations

Jordi Creus‐Muncunill, Jaroslav Bendl, Alexey Kozlenkov, Biao Zeng, Chuhyon Corwin +10 more

Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

Biological Psychiatry(2021)10.1016/j.biopsych.2020.12.024

N/A

0.673DataRank · unranked

88 citations

Ekaterina Khramtsova, Slavina B. Goleva, Gabriëlla A.M. Blokland, Michela Traglia, Raymond K. Walters +37 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

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

Epigenome-wide association study of depression symptomatology in elderly monozygotic twins

Translational Psychiatry(2019)10.1038/s41398-019-0548-9

N/A

0.641DataRank · unranked

71 citations

Q. Tan, M. Soerensen, M. McGue, O. Mors, Anders D. Børglum +4 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

Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling

medRxiv(2024)10.1101/2024.07.03.24309466

N/A

0.614DataRank · unranked

27 citations

Brad Verhulst, Silviu‐Alin Bacanu, Rosa Cheesman, Kirstin L. Purves, Hüseyin Gedik +95 more

Genetic Architecture of 11 Major Psychiatric Disorders at Biobehavioral, Functional Genomic, and Molecular Genetic Levels of Analysis

medRxiv(2020)10.1101/2020.09.22.20196089

N/A

0.606DataRank · unranked

56 citations

Travis T. Mallard, Wonuola A. Akingbuwa, Hill F. Ip, Mark J. Adams, Cathryn M. Lewis +16 more

Distinct genomic signatures and modifiable risk factors underly the comorbidity between major depressive disorder and cardiovascular disease

medRxiv(2023)10.1101/2023.09.01.23294931

N/A

0.600DataRank · unranked

7 citations

Joëlle A. Pasman, Ziyan Ma, Arvid Harder, Shuyang Yao, Nadine Parker +21 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

Examining sex-differentiated genetic effects across neuropsychiatric and behavioral traits

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.04.076042

N/A

0.567DataRank · unranked

13 citations

Ekaterina Khramtsova, Slavina B. Goleva, Gabriëlla A.M. Blokland, Michela Traglia, Raymond K. Walters +27 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

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

Molecular Psychiatry(2022)10.1038/s41380-022-01775-5

N/A

0.510DataRank · unranked

29 citations

Jeggan Tiego, Ditte Demontis, G. Bragi Walters, Hreinn Stefánsson, Kāri Stefánsson +4 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 risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

Translational Psychiatry(2023)10.1038/s41398-023-02341-5

N/A

0.494DataRank · unranked

26 citations

Tyne W. Miller‐Fleming, Apostolia Topaloudi, Dongmei Yu, Petros Drineas, Marianthi Georgitsi +89 more

Distinct genetic liability profiles define clinically relevant patient strata across common diseases

Nature Communications(2024)10.1038/s41467-024-49338-2

N/A

0.466DataRank · unranked

10 citations

Georgii Dolgalev, Sylvain Moser, Laura T. Jiménez-Barrón, Till F. M. Andlauer, Moritz von Scheidt +95 more

Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32951

Top 41%

0.456DataRank

Top 41%11 citations

Emma Sprooten, Peter Mulders, Janna N. Vrijsen, Janita Bralten, Ditte Demontis +8 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

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

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

Transcriptomic risk scores for attention deficit/hyperactivity disorder

Molecular Psychiatry(2023)10.1038/s41380-023-02200-1

N/A

0.425DataRank · unranked

16 citations

Natalia Llonga, Lorena Arribas, Silvia Alemany, Laura Vilar‐Ribó, Ditte Demontis +8 more

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.04.466897

N/A

0.406DataRank · unranked

14 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +85 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

Rare genetic variants confer a high risk of ADHD and implicate neuronal biology

Nature(2025)10.1038/s41586-025-09702-8

N/A

0.377DataRank · unranked

11 citations

Jinjie Duan, Yu-Han H. Hsu, Greta Pintacuda, Jakob Grove, Trine Tollerup Nielsen +29 more

Shared familial risk for type 2 diabetes mellitus and psychiatric disorders: a nationwide multigenerational genetics study

Psychological Medicine(2024)10.1017/s0033291724001053

N/A

0.345DataRank · unranked

9 citations

Isabell Brikell, Aske Astrup, Janne Tidselbak Larsen, Liselotte Petersen, Clara Albiñana +15 more

Polygenic liabilities and treatment trajectories in early-onset depression: a Danish register-based study

Psychological Medicine(2024)10.1017/s0033291724002186

Top 51%

0.345DataRank

Top 51%5 citations

Alisha S. M. Hall, Jette Steinbach, Clara Albiñana, Esben Agerbo, Thomas D. Als +9 more

The role of co-occurring conditions and genetics in the associations of eating disorders with attention-deficit/hyperactivity disorder and autism spectrum disorder

Molecular Psychiatry(2024)10.1038/s41380-024-02825-w

N/A

0.330DataRank · unranked

8 citations

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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

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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

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medRxiv(2021)10.1101/2021.07.13.21260299

N/A

0.269DataRank · unranked

5 citations

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medRxiv(2021)10.1101/2021.12.04.21267094

N/A

0.265DataRank · unranked

4 citations

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medRxiv(2024)10.1101/2024.09.23.24314234

N/A

0.256DataRank · unranked

4 citations

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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

Shared genetic architecture of posttraumatic stress disorder with cardiovascular imaging, risk, and diagnoses

Nature Communications(2025)10.1038/s41467-025-60487-w

N/A

0.208DataRank · unranked

3 citations

Wander Valentim, Eleni Friligkou, Cassie Overstreet, Karmel W. Choi, Dóra Koller +95 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

Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/790626

N/A

0.188DataRank · unranked

2 citations

Satish K. Nandakumar, Xiaotian Liao, Alexander G. Bick, Christel M. Middeldorp, Marcin Tabaka +30 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

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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

As rates of ASD and ADHD rise, genetic contributions fall: Evidence for widening diagnostic criteria

medRxiv(2025)10.1101/2025.11.10.25339891

N/A

0.165DataRank · unranked

2 citations

Mette Lise Lousdal, Morten Dybdahl Krebs, Ole Kromann Hansen, Kajsa-Lotta LA Georgii Hellberg, Mischa Lundberg +12 more

Multi-polygenic scores in psychiatry: from disorder-specific to transdiagnostic perspectives

medRxiv(2022)10.1101/2022.05.30.22275563

N/A

0.118DataRank · unranked

1 citations

Emma Sprooten, Peter Mulders, Janna N. Vrijsen, Janita Bralten, Ditte Demontis +8 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

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.31.494251

N/A

0.104DataRank · unranked

1 citations

Jeggan Tiego, Ditte Demontis, G. Bragi Walters, Hreinn Stefánsson, Kāri Stefánsson +4 more

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

medRxiv(2021)10.1101/2021.05.21.21257530

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0.104DataRank · unranked

1 citations

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Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32967

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0.104DataRank · unranked

1 citations

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medRxiv(2024)10.1101/2024.02.22.24303124

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0.104DataRank · unranked

1 citations

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

Genetic risk effects on psychiatric disorders act in sets

medRxiv(2025)10.1101/2025.07.23.25332043

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0.104DataRank · unranked

1 citations

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Shared Genetic Architecture Between Endometriosis and Psychiatric Conditions May Explain Comorbidity

medRxiv(2025)10.1101/2025.10.22.25338556

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0.104DataRank · unranked

1 citations

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Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

UNC Libraries(2020)10.17615/k3vg-tb84

N/A

0DataRank · unranked

0 citations

Stacy Steinberg, Johannes H. Smit, Tim B. Bigdeli, Kāri Stefánsson, Stefan Kloiber +71 more

The role of co-occurring conditions and genetics in the associations of eating disorders with attention-deficit/hyperactivity disorder and autism spectrum disorder

UNC Libraries(2024)10.17615/6vpf-k171

N/A

0DataRank · unranked

0 citations

Gitte Bundgaard Christiansen, K. E. Van Holde, Bjarni J. Vilhjálmsson, Christopher Hübel, Liselotte Petersen +13 more

Rare missense variants of the leukocyte common antigen related receptor (LAR) display reduced activity in transcellular adhesion and synapse formation

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.02.16.638491

N/A

0DataRank · unranked

0 citations

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Rare missense variants of the leukocyte common antigen related receptor (LAR) display reduced activity in transcellular adhesion and synapse formation

Research Square(2025)10.21203/rs.3.rs-5928514/v1

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0DataRank · unranked

0 citations

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Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 Patients

Biological Psychiatry Global Open Science(2025)10.1016/j.bpsgos.2025.100604

Top 100%

0DataRank

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

UNC Libraries(2024)10.17615/4537-h435

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0DataRank · unranked

0 citations

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medRxiv(2022)10.1101/2022.11.09.22281216

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0DataRank · unranked

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