Preben Bo Mortensen

Lundbeck Foundation

MedicineBiochemistry, Genetics and Molecular BiologyPsychologyNeuroscience

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

29.7Author 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.

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

Papers

Driven by 116 papers — median percentile 87. 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

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 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

Pan-cancer analysis of whole genomes

Nature(2020)10.1038/s41586-020-1969-6

Top 3%

5.9DataRank

Top 3%3307 citations

Lauri A. Aaltonen, Federico Abascal, Adam Abeshouse, Hiroyuki Aburatani, David J. Adams +1244 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

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

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

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

Nature(2020)10.1038/s41586-020-1965-x

Top 5%

4.6DataRank

Top 5%668 citations

Federico Abascal, Jeremiah A. Wala, Ofer Shapira, Grace Tiao, Henrik Hornshøj +1240 more

QRICH1 dictates the outcome of ER stress through transcriptional control of proteostasis

Science(2021)10.1126/science.abb6896

N/A

4.1DataRank · unranked

149 citations

Lingfei Wang, Chih-Hung Chou, Kai Liu, Toru Nakata, Alok Jaiswal +9 more

Assessment of Osteoarthritis Candidate Genes in a Meta‐Analysis of Nine Genome‐Wide Association Studies

Arthritis & Rheumatology(2014)10.1002/art.38300

Top 6%

3.9DataRank

Top 6%131 citations

Manuel Calaza, Evangelos Evangelou, Ana M. Valdes, Nigel Arden, Francisco J. Blanco +54 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 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

Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases

medRxiv(2020)10.1101/2020.09.08.20190561

N/A

3.4DataRank · unranked

132 citations

Jacob C. Ulirsch, Nathan Y. Cheng, Brian L. Trippe, Rebecca S. Fine, Jenkai Miao +24 more

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Nature Neuroscience(2016)10.1038/nn.4404

N/A

3.3DataRank · unranked

113 citations

Giulio Genovese, Daniel P. Howrigan, Andrea Byrnes, Mitja I Kurki, Seyedeh M. Zekavat +31 more

B cell genomics behind cross-neutralization of SARS-CoV-2 variants and SARS-CoV

Cell(2021)10.1016/j.cell.2021.04.032

N/A

2.9DataRank · unranked

100 citations

Christopher O. Barnes, Basak Eraslan, Andrew Hudak, Jennifer R. Keeffe, Lisa A. Cosimi +34 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

Colon stroma mediates an inflammation-driven fibroblastic response controlling matrix remodeling and healing

PLOS Biology(2022)10.1371/journal.pbio.3001532

N/A

2.7DataRank · unranked

107 citations

Alok Jaiswal, Mukund Varma, Tyler Laszewski, Angelo Grauel, Abdifatah S. Omar +11 more

Spatial host–microbiome sequencing reveals niches in the mouse gut

Nature Biotechnology(2023)10.1038/s41587-023-01988-1

N/A

2.7DataRank · unranked

121 citations

Martin Stražar, James G. Wilson, Prisca Liberali, Sanja Vicković, Preben Bo Mortensen +1 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

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

The DOT1L rs12982744 polymorphism is associated with osteoarthritis of the hip with genome-wide statistical significance in males

Annals of the Rheumatic Diseases(2013)10.1136/annrheumdis-2012-203182

N/A

2.3DataRank · unranked

60 citations

Ana M. Valdes, Martha C Castano-Betancourt, Sally Doherty, Tonu Esko, Thorvaldur Ingvarsson +21 more

An open resource of structural variation for medical and population genetics

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/578674

Top 9%

2.2DataRank

Top 9%44 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +37 more

The Human Cell Atlas White Paper

arXiv (Cornell University)(2018)10.17863/cam.40032

Top 10%

2.2DataRank

Top 10%41 citations

Sarah A. Teichmann, Orit Rozenblatt‐Rosen, Michael J. T. Stubbington, Kristin G. Ardlie, Ido Amit +76 more

An Integrated Taxonomy for Monogenic Inflammatory Bowel Disease

Gastroenterology(2022)10.1053/j.gastro.2021.11.014

N/A

2.0DataRank · unranked

95 citations

Christopher S. Smillie, Sumeet Pandey, Rasa Elmentaite, Gabrielle Wei, Carmen Argmann +35 more

Single-cell profiling of proteins and chromatin accessibility using PHAGE-ATAC

Nature Biotechnology(2021)10.1038/s41587-021-01065-5

N/A

2.0DataRank · unranked

69 citations

Caleb A. Lareau, Leif S. Ludwig, Gökçen Eraslan, Feimei Liu, Aaron M. Ring +3 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

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

The American Journal of Human Genetics(2007)10.1086/519795

N/A

1.6DataRank · unranked

35753 citations

Preben Bo Mortensen, Kathe Todd-Brown, Lori Thomas, Manuel A.R. Ferreira, David Bender +12 more

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 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

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

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

Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults

The Lancet(2017)10.1016/s0140-6736(17)32129-3

N/A

1.3DataRank · unranked

7558 citations

Ziad A Abdeen, Zargar Abdul Hamid, Niveen M Abu-Rmeileh, Benjamin Acosta-Cazares, Cecilia Acuin +1262 more

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

An esophagus cell atlas reveals dynamic rewiring during active eosinophilic esophagitis and remission

Nature Communications(2024)10.1038/s41467-024-47647-0

N/A

1.3DataRank · unranked

57 citations

John J. Garber, Amiko Uchida, Ariel Lefkovith, Grace T. Carter, Praveen Vimalathas +14 more

Prediction of Autism Risk From Family Medical History Data Using Machine Learning: A National Cohort Study From Denmark

Biological Psychiatry Global Open Science(2021)10.1016/j.bpsgos.2021.04.007

Top 17%

1.2DataRank

Top 17%34 citations

Jesper Wulff, Amy E. Kalkbrenner, Christine Ladd‐Acosta, M. Danielle Fallin, Esben Agerbo +4 more

Distinct Tissue-Specific Roles for the Disease-Associated Autophagy Genes ATG16L2 and ATG16L1

The Journal of Immunology(2019)10.4049/jimmunol.1800419

N/A

1.2DataRank · unranked

32 citations

Kara L. Conway, Abdifatah S. Omar, Moshe Biton, Adam L. Haber, Noga Rogel +8 more

Induction of a colitogenic phenotype in Th1-like cells depends on interleukin-23 receptor signaling

Immunity(2022)10.1016/j.immuni.2022.08.007

N/A

1.2DataRank · unranked

49 citations

David DeTomaso, Alexandra Schnell, Youjin Lee, Jackson Nyman, Danielle Dionne +15 more

A Roadmap for the Human Gut Cell Atlas

Nature Reviews Gastroenterology & Hepatology(2023)10.1038/s41575-023-00784-1

Top 17%

1.2DataRank

Top 17%51 citations

Kylie R. James, Mandeep Kaur, Sebastian Pott, Zhixin Li, Albert Burger +37 more

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 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

Temporal development of the gut microbiome in early childhood from the TEDDY study

Nature(2018)10.1038/s41586-018-0617-x

N/A

1.1DataRank · unranked

2041 citations

Nadim J. Ajami, Jacqueline L. O’Brien, Diane S. Hutchinson, Daniel P. Smith, Matthew C. Wong +28 more

CRISPR-Cas9 Knockin Mice for Genome Editing and Cancer Modeling

Cell(2014)10.1016/j.cell.2014.09.014

N/A

1.1DataRank · unranked

2034 citations

Sidi Chen, Yang Zhou, Michael J. Yim, Lukasz Swiech, Hannah R. Kempton +17 more

A single-cell survey of the small intestinal epithelium

Nature(2017)10.1038/nature24489

N/A

1.1DataRank · unranked

1850 citations

Moshe Biton, Noga Rogel, Rebecca H. Herbst, Karthik Shekhar, Indresh Singh +18 more

Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance

Journal of Medical Genetics(2014)10.1136/jmedgenet-2014-102478

N/A

1.1DataRank · unranked

25 citations

Sarah Metrustry, Nigel Arden, Anne C Bay-Jensen, Marian Beekman, Anton J. M. de Craen +28 more

Rewiring of the cellular and inter-cellular landscape of the human colon during ulcerative colitis

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/455451

N/A

1.1DataRank · unranked

19 citations

Moshe Biton, Keri M. Sullivan, Grace Burgin, Daniel B. Graham, Rebecca H. Herbst +24 more

Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis

Cell(2019)10.1016/j.cell.2019.06.029

N/A

1.1DataRank · unranked

1412 citations

Moshe Biton, Keri M. Sullivan, Grace Burgin, Daniel B. Graham, Rebecca H. Herbst +28 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

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 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

The Human and Mouse Enteric Nervous System at Single-Cell Resolution

Cell(2020)10.1016/j.cell.2020.08.003

N/A

0.948DataRank · unranked

556 citations

Christopher S. Smillie, Nicholas Van Wittenberghe, Maria Ericsson, Gabriel K. Griffin, David S. Fischer +14 more

Remodeling of colon plasma cell repertoire within ulcerative colitis patients

Journal of Experimental Medicine(2023)10.1084/jem.20220538

N/A

0.939DataRank · unranked

31 citations

Basak Eraslan, Andrew Hudak, Eric M. Brown, Dallis Sergio, Toni Marie Delorey +13 more

Raman2RNA: Live-cell label-free prediction of single-cell RNA expression profiles by Raman microscopy

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.30.470655

N/A

0.911DataRank · unranked

18 citations

Shreya Gaddam, Taylor James-Sorenson, Emanuelle Grody, Johain R. Ounadjela, Baoliang Ge +10 more

The enteric nervous system of the human and mouse colon at a single-cell resolution

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/746743

N/A

0.905DataRank · unranked

24 citations

Christopher S. Smillie, Nicholas Van Wittenberghe, Maria Ericsson, Gabriel K. Griffin, Danielle Dionne +11 more

Pathogen Cell-to-Cell Variability Drives Heterogeneity in Host Immune Responses

Cell(2015)10.1016/j.cell.2015.08.027

N/A

0.878DataRank · unranked

347 citations

Nathan Haseley, Douglas Brown, Cristina Penaranda, John J. Trombetta, Rahul Satija +7 more

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature Genetics(2013)10.1038/ng.2543

N/A

0.862DataRank · unranked

313 citations

Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel +43 more

Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases

Nature Genetics(2023)10.1038/s41588-023-01443-6

N/A

0.853DataRank · unranked

293 citations

Jacob C. Ulirsch, Nathan Y. Cheng, Brian L. Trippe, Rebecca S. Fine, Jenkai Miao +23 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

Calcitonin Gene-Related Peptide Negatively Regulates Alarmin-Driven Type 2 Innate Lymphoid Cell Responses

Immunity(2019)10.1016/j.immuni.2019.09.005

N/A

0.823DataRank · unranked

241 citations

Patrick R. Burkett, Samantha J. Riesenfeld, Se-Jin Kim, Elena Christian, Raja-Elie E. Abdulnour +12 more

Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics

Nature Genetics(2022)10.1038/s41588-022-01187-9

N/A

0.820DataRank · unranked

235 citations

Kushal K. Dey, Daniel T. Montoro, Rahul Mohan, Steven Gazal, Jesse M. Engreitz +4 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

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

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

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

Author response: The Human Cell Atlas

(2017)10.7554/elife.27041.011

Top 29%

0.700DataRank

Top 29%14 citations

Sarah A. Teichmann, Matthew E. Hurles, Ido Amit, Kerstin Lindblad‐Toh, Bernd Bodenmiller +60 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

Spatial host-microbiome sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.07.18.500470

N/A

0.614DataRank · unranked

13 citations

Martin Stražar, Preben Bo Mortensen, Prisca Liberali, Sanja Vicković, Britta Lötstedt

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

Multi-modal skin atlas identifies a multicellular immune-stromal community associated with altered cornification and specific T cell expansion in atopic dermatitis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.29.563503

N/A

0.564DataRank · unranked

11 citations

Gökçen Eraslan, Maria Beatrice Alora, Juan Manuel Leyva-Castillo, Sean Kim, Heather Choe +24 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

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

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

T helper cells modulate intestinal stem cell renewal and differentiation

bioRxiv (Cold Spring Harbor Laboratory)(2017)10.1101/217133

N/A

0.368DataRank · unranked

5 citations

Adam L. Haber, Semir Beyaz, Noga Rogel, Indresh Singh, Karthik Shekhar +26 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Pathogen Cell-to-Cell Variability Drives Heterogeneity in Host Immune Responses

Cell(2015)10.1016/j.cell.2015.09.044

N/A

0.241DataRank · unranked

4 citations

Nathan Haseley, Douglas Brown, Cristina Penaranda, John J. Trombetta, Rahul Satija +8 more

356 COMMON VARIANTS IN SKELETAL DYSPLASIA GENES ARE ASSOCIATED WITH OSTEOARTHRITIS

Osteoarthritis and Cartilage(2011)10.1016/s1063-4584(11)60383-x

N/A

0.210DataRank · unranked

3 citations

M. Irving, Katharina Domschke, Unnur Styrkarsdottir, Y. Zhu, Aravinda Chakravarti +34 more

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Communications Biology(2022)10.1038/s42003-022-03769-z

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0.165DataRank · unranked

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Research Square(2022)10.21203/rs.3.rs-1416969/v1

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0.104DataRank · unranked

1 citations

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medRxiv(2021)10.1101/2021.02.12.21250941

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0DataRank · unranked

8 citations

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medRxiv(2021)10.1101/2021.07.13.21260299

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0DataRank · unranked

5 citations

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medRxiv(2021)10.1101/2021.10.04.21264526

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0DataRank · unranked

2 citations

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medRxiv(2021)10.1101/2021.05.21.21257530

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0DataRank · unranked

1 citations

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

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0DataRank · unranked

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UNC Libraries(2021)10.17615/8vy9-q427

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0DataRank · unranked

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

Frontiers in Genetics(2021)10.3389/fgene.2021.711624

N/A

0DataRank · unranked

17 citations

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

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Brain(2021)10.1093/brain/awab260

N/A

0DataRank · unranked

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UCL Discovery (University College London)(2020)10.17615/snbr-qh40

N/A

0DataRank · unranked

0 citations

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

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0DataRank · unranked

29 citations

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Psychological Medicine(2022)10.1017/s0033291721004554

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The Lancet Digital Health(2022)10.1016/s2589-7500(22)00099-1

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0DataRank · unranked

18 citations

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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

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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

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medRxiv(2022)10.1101/2022.06.08.22276164

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medRxiv(2022)10.1101/2022.11.09.22281216

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0DataRank · unranked

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

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18 citations

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Nature Communications(2022)10.1038/s41467-022-32343-8

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

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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

UNC Libraries(2020)10.17615/2bje-6g29

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0DataRank · unranked

0 citations

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

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

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0DataRank · unranked

28 citations

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medRxiv(2025)10.1101/2025.09.19.25334095

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

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3-generation family histories of mental, neurologic, cardiometabolic, birth defect, asthma, allergy, and autoimmune conditions associated with autism: an open-source catalogue of findings

medRxiv(2023)10.1101/2023.11.03.23298042

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Psychological Medicine(2024)10.1017/s0033291724001053

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9 citations

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

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8 citations

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Autism Research(2024)10.1002/aur.3232

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Linda Ejlskov, Morten Overgaard, Zeal Jinwala, Viktor Kim, Erik Thorlund Parner +7 more

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bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.14.480403

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medRxiv(2024)10.1101/2024.09.23.24314234

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0DataRank · unranked

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UNC Libraries(2024)10.17615/6vpf-k171

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bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.16.649031

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