Aarno Palotie

Also affiliated with University of Helsinki, Massachusetts General Hospital, Research Institute for Music Theater Studies, Institute for Molecular Medicine Finland

Biochemistry, Genetics and Molecular BiologyEnvironmental ScienceEarth and Planetary Sciences

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

39.6Author DataRank

Indexed papers

7in 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 7 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.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 97 papers — median percentile 97. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

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

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534

Top 2%

9.1DataRank

Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 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

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111

Top 3%

6.7DataRank

Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 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

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

The GENCODE exome: sequencing the complete human exome

European Journal of Human Genetics(2011)10.1038/ejhg.2011.28

Top 5%

4.1DataRank

Top 5%64 citations

Felix Kokocinski, Maria S Calafato, Carol E Scott, Priit Palta, Eleanor Drury +9 more

Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

Nature(2020)10.1038/s41586-020-2786-7

N/A

4.1DataRank · unranked

151 citations

Satish K. Nandakumar, Xiaotian Liao, Alexander G. Bick, Juha Karjalainen, Marcin Tabaka +79 more

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

Nature Communications(2022)10.1038/s41467-022-29143-5

N/A

3.9DataRank · unranked

196 citations

Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke +33 more

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Nature Genetics(2022)10.1038/s41588-022-01156-2

N/A

3.7DataRank · unranked

195 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu +95 more

Genome-wide association study identifies 48 common genetic variants associated with handedness

Nature Human Behaviour(2020)10.1038/s41562-020-00956-y

N/A

3.7DataRank · unranked

157 citations

Joyce Y. Tung, Nicholas Eriksson, Eva Albrecht, Fazil Alıev, Ole A. Andreassen +95 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

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

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

Genome Research(2010)10.1101/gr.106534.110

N/A

2.6DataRank · unranked

61 citations

Kati Kristiansson, Verneri Anttila, Michael Inouye, Chris Barnes, Loukas Moutsianas +6 more

Genome-wide risk prediction of common diseases across ancestries in one million people

Cell Genomics(2022)10.1016/j.xgen.2022.100118

N/A

2.3DataRank · unranked

93 citations

Sini Kerminen, Yen‐Chen Anne Feng, Masahiro Kanai, Kristi Läll, Laurent F. Thomas +15 more

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set

Cephalalgia(2016)10.1177/0333102414566820

N/A

1.6DataRank · unranked

61 citations

Verneri Anttila, Tobias Freilinger, Maija Wessman, Mari A Kaunisto, Mikko Kallela +10 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

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

Nature Communications(2022)10.1038/s41467-022-31436-8

N/A

1.4DataRank · unranked

61 citations

Olli Pietiläinen, Mykyta Artomov, Matthew Tegtmeyer, Vera Valakh, Leevi Lehtonen +40 more

Combined effects of genotype and childhood adversity shape variability of DNA methylation across age

Translational Psychiatry(2021)10.1038/s41398-020-01147-z

N/A

1.4DataRank · unranked

50 citations

Elleke Tissink, Johanna Tuhkanen, Jade Martins, Yvonne Awaloff, Amanda J. Drake +19 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

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

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

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nature Communications(2021)10.1038/s41467-021-22339-1

N/A

1.1DataRank · unranked

51 citations

Akhil Pampana, Sarah E. Graham, Sanni Ruotsalainen, James A. Perry, Paul S. de Vries +95 more

Genomic prediction of alcohol-related morbidity and mortality

Translational Psychiatry(2020)10.1038/s41398-019-0676-2

N/A

1.1DataRank · unranked

30 citations

Nina Mars, Teemu Palviainen, Jukka Koskela, Joel Rämö, Pietari Ripatti +10 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

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature Genetics(2012)10.1038/ng.2274

N/A

1.0DataRank · unranked

897 citations

Marie-France Hivert, Robert A Scott, Jonna L Grimsby, Nabila Bouatia-Naji, Han Chen +211 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

The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

EBioMedicine(2023)10.1016/j.ebiom.2023.104630

N/A

1.0DataRank · unranked

28 citations

Fahrisa I. Maisha, Satu Strausz, Vilma Lammi, Brian E. Cade, Anniina Tervi +88 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

Deep learning of left atrial structure and function provides link to atrial fibrillation risk

Nature Communications(2024)10.1038/s41467-024-48229-w

N/A

0.931DataRank · unranked

38 citations

Paolo Di Achille, Seung Hoan Choi, Joel Rämö, Shaan Khurshid, Mahan Nekoui +14 more

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Nature Genetics(2022)10.1038/s41588-021-00990-0

N/A

0.900DataRank · unranked

402 citations

Bendik Slagsvold Winsvold, Sanni Ruotsalainen, Gyða Björnsdóttir, Aster V. E. Harder, Lisette J. A. Kogelman +68 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

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

Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

Stroke(2023)10.1161/strokeaha.123.043052

N/A

0.706DataRank · unranked

27 citations

Anni Kauko, Sarah E. Tom, Hannele Laivuori, Teemu Niiranen, Natalie A. Bello +86 more

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

Työväentutkimus Vuosikirja(2020)10.1161/circgen.119.002725

N/A

0.700DataRank · unranked

105 citations

Pietari Ripatti, Joel Rämö, Nina Mars, Yu Fu, Jake Lin +15 more

Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

Nature Communications(2023)10.1038/s41467-023-35974-7

N/A

0.680DataRank · unranked

22 citations

Jaakko Tyrmi, Nilüfer Rahmioğlu, Krina T. Zondervan, Christian M. Becker, FinnGen +95 more

Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

Nature Genetics(2024)10.1038/s41588-023-01607-4

N/A

0.663DataRank · unranked

82 citations

Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jacqueline I. Goldstein +23 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

The impact of rare protein coding genetic variation on adult cognitive function

Nature Genetics(2023)10.1038/s41588-023-01398-8

N/A

0.628DataRank · unranked

65 citations

Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh +76 more

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Nature Genetics(2024)10.1038/s41588-024-01975-5

N/A

0.601DataRank · unranked

54 citations

Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin +55 more

Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

Nature Communications(2022)10.1038/s41467-022-32885-x

N/A

0.578DataRank · unranked

46 citations

Wei Zhou, Tuomo Kiiskinen, Aki S. Havulinna, Amanda Elliott, Juha Karjalainen +9 more

Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction

Nature Communications(2024)10.1038/s41467-024-53595-6

N/A

0.533DataRank · unranked

14 citations

Sudhanshu Shekhar, Daniel F. Levey, Péter Straub, Julia Kraft, Georgia Panagiotaropoulou +35 more

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

medRxiv(2021)10.1101/2021.06.15.21258641

N/A

0.500DataRank · unranked

11 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, María T. Abreu +95 more

Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics

Neuropsychopharmacology(2021)10.1038/s41386-021-01023-4

N/A

0.489DataRank · unranked

25 citations

Chia‐Yen Chen, Tian Ge, Yan Xia, David W. Hill, Joey W. Trampush +66 more

Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

Nature Communications(2024)10.1038/s41467-024-50295-z

N/A

0.489DataRank · unranked

25 citations

Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie +4 more

High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

Nature Communications(2024)10.1038/s41467-024-53634-2

N/A

0.477DataRank · unranked

23 citations

Pekka Nieminen, Priyanka Kumari, Emma Juuri, Tiit Nikopensius, Kitt Paraiso +24 more

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.123.004320

N/A

0.413DataRank · unranked

10 citations

Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N. Morrill, Yan V. Sun +54 more

An efficient and accurate frailty model approach for genome-wide survival association analysis controlling for population structure and relatedness in large-scale biobanks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.31.358234

N/A

0.385DataRank · unranked

12 citations

Wei Zhou, Tuomo Kiiskinen, Aki S. Havulinna, Amanda Elliott, Juha Karjalainen +9 more

Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders

Molecular Psychiatry(2024)10.1038/s41380-024-02516-6

N/A

0.360DataRank · unranked

10 citations

Jaana Suvisaari, Markku Lähteenvuo, Tarjinder Singh, Ari Ahola‐Olli, Lea Urpa +33 more

Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection

medRxiv(2023)10.1101/2023.01.28.23285140

N/A

0.312DataRank · unranked

7 citations

Giulio Genovese, Yajie Zhao, Matti Pirinen, Maryam M. Zekavat, Katherine A. Kentistou +39 more

Identifying Nootropic Drug Targets via Large-Scale Cognitive GWAS and Transcriptomics

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.06.934752

N/A

0.312DataRank · unranked

7 citations

Chen Chia-Yen, Xia Yan, W. David Hill, Joey W. Trampush, Jin Yu +64 more

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 more

Narcolepsy as a potential risk factor for Schizophrenia

Translational Psychiatry(2025)10.1038/s41398-025-03259-w

N/A

0.248DataRank · unranked

3 citations

Anniina Tervi, Samuel E. Jones, FinnGen, Aarno Palotie, Mark Daly +95 more

Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

medRxiv(2023)10.1101/2023.11.27.23297542

N/A

0.241DataRank · unranked

4 citations

Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie +3 more

Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk

Nature Genetics(2025)10.1038/s41588-025-02397-7

N/A

0.241DataRank · unranked

4 citations

Joel Rämö, Cody R. Hou, Sean J. Jurgens, Shaan Khurshid, Victor Nauffal +12 more

Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts

EClinicalMedicine(2024)10.1016/j.eclinm.2024.102956

N/A

0.214DataRank · unranked

3 citations

Lindsay Wilson, Daniel F. Levey, Livia Parodi, Ewout W. Steyerberg, Sylvia Richardson +95 more

Genome-wide association study of 1,391 plasma metabolites in 6,136 Finnish men identifies 303 novel signals and provides biological insights into human diseases

medRxiv(2021)10.1101/2021.10.19.21265094

N/A

0.208DataRank · unranked

3 citations

Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke +32 more

Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

Alzheimer s Research & Therapy(2024)10.1186/s13195-023-01376-6

N/A

0.208DataRank · unranked

3 citations

Jeannette Simino, Lianna Li, Fan Jiang, Joshua C. Bis, Gail Davies +62 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

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Nature Medicine(2021)10.1038/s41591-021-01371-0

N/A

0DataRank · unranked

193 citations

Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang +95 more

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

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

N/A

0DataRank · unranked

0 citations

Kung‐Yee Liang, Per Hoffman, Stefan Herms, Gary Donohoe, Luba Kalaydjieva +94 more

Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

UNC Libraries(2020)10.17615/xs3t-3334

N/A

0DataRank · unranked

0 citations

Annette L. Fitzpatrick, Luigi Ferrucci, Paul M. Ridker, Bertram Müller-Myhsok, Arezoo Assareh +95 more

New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk

Research at the University of Copenhagen (University of Copenhagen)(2020)10.17615/07fz-zt78

N/A

0DataRank · unranked

0 citations

Stavroula Kanoni, Ghazaleh Fatemifar, Tiina Laatikainen, Cristina Menni, Yingchang Lu +95 more

Distinct and shared genetic architectures of Gestational diabetes mellitus and Type 2 Diabetes Mellitus

medRxiv(2023)10.1101/2023.02.16.23286014

N/A

0DataRank · unranked

10 citations

Raymond K. Walters, Matti Pirinen, Mitja Kurki, Nella Junna, Jonathan T. Goldstein +9 more

Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health

medRxiv(2023)10.1101/2023.06.26.23291721

N/A

0DataRank · unranked

8 citations

Jack Li, Debraj Bose, Jeffrey Okamoto, Annie Kwon, Anne Jackson +14 more

Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

medRxiv(2020)10.1101/2020.11.15.20227868

N/A

0DataRank · unranked

4 citations

Tuomo Kiiskinen, Juha Karjalainen, Kristi Krebs, Mitja Kurki, Aki S. Havulinna +17 more

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

medRxiv(2023)10.1101/2023.09.24.23295485

N/A

0DataRank · unranked

0 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +56 more

High heritability of ascending aortic diameter and multi-ethnic prediction of thoracic aortic disease.

medRxiv(2020)10.1101/2020.05.29.20102335

N/A

0DataRank · unranked

9 citations

Ke Xiao, Heliodoro Tejeda, Julie A. Lynch, Sanni Ruotsalainen, Tiffany R. Bellomo +17 more

Polygenic risk, susceptibility genes, and breast cancer over the life course

medRxiv(2020)10.1101/2020.04.17.20069229

N/A

0DataRank · unranked

11 citations

Elisabeth Widén, Sini Kerminen, Tuomo J Meretoja, Matti Pirinen, Priit Palta +7 more

Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.007

N/A

0DataRank · unranked

62 citations

Debraj Bose, Annie Kwon, Sarah C. Hanks, Anne Jackson, Heather M. Stringham +24 more

Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

PLoS Genetics(2020)10.1371/journal.pgen.1008682

N/A

0DataRank · unranked

53 citations

Michael Wainberg, Juha Karjalainen, Tuomo Kiiskinen, Guhan Venkataraman, Susanna Lemmelä +9 more

Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

Blood(2024)10.1182/blood.2023023326

N/A

0DataRank · unranked

24 citations

Joel Rämö, Sean J. Jurgens, Teemu Niiranen, Simone Sanna‐Cherchi, Kenneth A. Bauer +7 more

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Brain(2020)10.1093/brain/awaa171

N/A

0DataRank · unranked

81 citations

Eduardo Pérez‐Palma, Daniel P. Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus +86 more

GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

Nature Communications(2020)10.1038/s41467-020-17718-z

N/A

0DataRank · unranked

141 citations

Ben Brumpton, Ömer Kabil, Jūlı́us Guðmundsson, Guðmar Þorleifsson, Joshua S. Weinstock +51 more

Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants

Nature Communications(2026)10.1038/s41467-025-64880-3

N/A

0DataRank · unranked

0 citations

Joonas Kartau, FinnGen, Aarno Palotie, Matti Pirinen, International Headache Genetics Consortium +1 more

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

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0 citations

Deborah J. Thompson, Hannes Helgason, Timothy M. Frayling, Hilary K. Finucane, Patrick Sulem +211 more

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Cell Genomics(2024)10.1016/j.xgen.2024.100630

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5 citations

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medRxiv(2024)10.1101/2024.07.09.24310146

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1 citations

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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more

Mapping and characterization of structural variation in 17,795 human genomes

UNC Libraries(2024)10.17615/bjv3-ys88

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S.S. Rich, Elizabeth L. Appelbaum, Ryan M. Layer, Subra Kugathasan, Scott M. Damrauer +95 more

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UNC Libraries(2024)10.17615/14dq-dd86

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0DataRank · unranked

0 citations

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Nature Communications(2025)10.1038/s41467-025-58686-6

N/A

0DataRank · unranked

11 citations

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medRxiv(2025)10.64898/2025.12.03.25341518

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0 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.30.927822

N/A

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15 citations

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Molecular Psychiatry(2022)10.1038/s41380-022-01828-9

N/A

0DataRank · unranked

69 citations

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European Journal of Human Genetics(2022)10.1038/s41431-022-01046-5

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16 citations

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medRxiv(2021)10.1101/2021.12.15.21267719

N/A

0DataRank · unranked

1 citations

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medRxiv(2022)10.1101/2022.10.31.22281753

N/A

0DataRank · unranked

2 citations

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medRxiv(2022)10.1101/2022.11.30.22282752

N/A

0DataRank · unranked

0 citations

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Science(2023)10.1126/science.abn9257

N/A

0DataRank · unranked

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N/A

0DataRank · unranked

86 citations

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