Lars G. Fritsche

Medicine

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

22.0Author DataRank

Indexed papers

17in 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 17 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 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

Papers

Driven by 71 papers — median percentile 68. Top paper: “A global reference for human genetic variation”.

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

A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

Nature Genetics(2021)10.1038/s41588-021-00921-z

N/A

8.0DataRank · unranked

1105 citations

Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Dominic Holland +95 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

4.0DataRank · unranked

141 citations

Ben Brumpton, Ömer Kabil, Jūlı́us Guðmundsson, Guðmar Þorleifsson, Joshua S. Weinstock +51 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 Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients

Cell Genomics(2023)10.1016/j.xgen.2023.100257

Top 10%

2.2DataRank

Top 10%98 citations

Lars G. Fritsche, Anita Pandit, Brett Vanderwerff, Snehal Patil, Ellen M. Schmidt +9 more

Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease

Gut(2021)10.1136/gutjnl-2020-323868

N/A

2.1DataRank · unranked

44 citations

David Ellinghaus, Simonas Juzėnas, François Cossais, Greta Burmeister, Gabriele Mayr +80 more

Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb

PLOS Genetics(2019)10.1371/journal.pgen.1008202

N/A

1.7DataRank · unranked

35 citations

Lauren J. Beesley, Peter VandeHaar, Robert B. Peng, Maxwell Salvatore, Matthew Zawistowski +13 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

1.6DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

PLoS Genetics(2020)10.1371/journal.pgen.1008725

Top 13%

1.6DataRank

Top 13%57 citations

Judith M. Vonk, Hansjörg Baurecht, Ingo Marenholz, Chao Tian, Joshua Hoffman +36 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

Largest GWAS (N=1,126,563) of Alzheimer’s Disease Implicates Microglia and Immune Cells

medRxiv(2020)10.1101/2020.11.20.20235275

N/A

1.5DataRank · unranked

43 citations

Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Arvid Rongve +52 more

The HUNT study: A population-based cohort for genetic research

Cell Genomics(2022)10.1016/j.xgen.2022.100193

Top 14%

1.5DataRank

Top 14%108 citations

Sarah E. Graham, Ida Surakka, Anne Heidi Skogholt, Mari Løset, Lars G. Fritsche +25 more

Single-cell multi-cohort dissection of the schizophrenia transcriptome

Science(2024)10.1126/science.adg5136

N/A

1.3DataRank · unranked

125 citations

Shahin Mohammadi, José Dávila-Velderrain, Sivan Subburaju, Daniel Reed Tso, Makayla Hourihan +196 more

ExPRSweb: An online repository with polygenic risk scores for common health-related exposures

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.001

Top 16%

1.3DataRank

Top 16%43 citations

Snehal Patil, Xiang Zhou, Bhramar Mukherjee, Lars G. Fritsche, Ying Ma

Massively parallel characterization of regulatory elements in the developing human cortex

Science(2024)10.1126/science.adh0559

N/A

1.2DataRank · unranked

61 citations

Sean Whalen, Marilyn Steyert, Ryan Ziffra, Pawel F. Przytycki, Fumitaka Inoue +197 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

Mitochondrial genome-wide association study of migraine – the HUNT Study

Cephalalgia(2020)10.1177/0333102420906835

Top 19%

1.1DataRank

Top 19%28 citations

John‐Anker Zwart, Anne Heidi Skogholt, Maiken E. Gabrielsen, Laurent F. Thomas, Lars G. Fritsche +13 more

A Phenome-Wide Association Study (PheWAS) of COVID-19 Outcomes by Race Using the Electronic Health Records Data in Michigan Medicine

Journal of Clinical Medicine(2021)10.3390/jcm10071351

Top 20%

1.0DataRank

Top 20%30 citations

Tian Gu, Jasmine A. Mack, Swaraaj Prabhu Sankar, Snehal Patil, Thomas S. Valley +7 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

Characteristics Associated With Racial/Ethnic Disparities in COVID-19 Outcomes in an Academic Health Care System

JAMA Network Open(2020)10.1001/jamanetworkopen.2020.25197

N/A

0.826DataRank · unranked

246 citations

Jasmine A. Mack, Maxwell Salvatore, Swaraaj Prabhu Sankar, Thomas S. Valley, Karandeep Singh +6 more

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Nature Genetics(2020)10.1038/s41588-020-0611-8

N/A

0.825DataRank · unranked

243 citations

D. Timothy Bishop, Stuart MacGregor, Mitchell J. Machiela, Alexander Stratigos, Paola Ghiorzo +95 more

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Cell Genomics(2023)10.1016/j.xgen.2022.100241

N/A

0.710DataRank · unranked

113 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +83 more

A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.003

N/A

0.677DataRank · unranked

90 citations

Lars G. Fritsche, Bhramar Mukherjee, Sehee Kim, Seunggeun Lee, Wenjian Bi

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

Cell Genomics(2022)10.1016/j.xgen.2022.100210

N/A

0.670DataRank · unranked

86 citations

Roy Elzur, Wei Zhou, Kuan-Han Wu, Humaira Rasheed, Kristin Tsuo +91 more

Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools

Brain(2021)10.1093/brain/awab267

N/A

0.633DataRank · unranked

67 citations

Guy Hindley, Bendik Slagsvold Winsvold, Kevin S. O’Connell, Oleksandr Frei, Alexey Shadrin +35 more

COVID-19 Outcomes by Cancer Status, Site, Treatment, and Vaccination

Cancer Epidemiology Biomarkers & Prevention(2023)10.1158/1055-9965.epi-22-0607

Top 32%

0.614DataRank

Top 32%13 citations

Miriam M. Hu, Lauren J. Beesley, Alison M. Mondul, Celeste Leigh Pearce, Christopher R. Friese +3 more

A phenome-wide association study (PheWAS) of COVID-19 outcomes by race using the electronic health records data in Michigan Medicine

medRxiv(2020)10.1101/2020.06.29.20141564

Top 34%

0.581DataRank

Top 34%4 citations

Tian Gu, Jasmine A. Mack, Swaraaj Prabhu Sankar, Snehal Patil, Thomas S. Valley +7 more

Correction: Systemic Complement Activation in Age-Related Macular Degeneration

PLoS ONE(2008)10.1371/annotation/32b9bc31-ed6d-4d31-9ce0-480407017bad

N/A

0.571DataRank · unranked

44 citations

Peter Charbel Issa, Maja Walier, Stefanie Janzer, Beatrix Pollok-Kopp, Florian Börncke +8 more

Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

Nature Genetics(2024)10.1038/s41588-024-01764-0

N/A

0.561DataRank · unranked

41 citations

Georgios Voloudakis, Robert P. Igo, Tyler G. Kinzy, Christopher Halladay, Tim B. Bigdeli +94 more

A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans

Communications Biology(2024)10.1038/s42003-024-06101-z

N/A

0.470DataRank · unranked

22 citations

Ailin Falkmo Hansen, Brooke N. Wolford, Laurent F. Thomas, Humaira Rasheed, Anica Simić +19 more

Patterns of repeated diagnostic testing for COVID‐19 in relation to patient characteristics and outcomes

Journal of Internal Medicine(2020)10.1111/joim.13213

N/A

0.449DataRank · unranked

19 citations

Zhangchen Zhao, Swaraaj Prabhu Sankar, Maxwell Salvatore, Tian Gu, Lars G. Fritsche +5 more

To weight or not to weight? The effect of selection bias in 3 large electronic health record-linked biobanks and recommendations for practice

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae098

N/A

0.416DataRank · unranked

15 citations

Ritoban Kundu, Xu Shi, Christopher R. Friese, Seunggeun Lee, Lars G. Fritsche +5 more

Cancer PRSweb – an Online Repository with Polygenic Risk Scores (PRS) for Major Cancer Traits and Their Phenome-wide Exploration in Two Independent Biobanks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.22.915751

Top 47%

0.389DataRank

Top 47%4 citations

Snehal Patil, Lauren J. Beesley, Peter VandeHaar, Maxwell Salvatore, Robert B. Peng +4 more

Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration

Human Molecular Genetics(2023)10.1093/hmg/ddad189

N/A

0.385DataRank · unranked

12 citations

Matthew Zawistowski, Lars G. Fritsche, Xiaowei Zhan, Jennifer L. Bragg‐Gresham, Kari Branham +9 more

Using Multi-Modal Electronic Health Record Data for the Development and Validation of Risk Prediction Models for Long COVID Using the Super Learner Algorithm

Journal of Clinical Medicine(2023)10.3390/jcm12237313

Top 50%

0.357DataRank

Top 50%6 citations

Wei Hao, Xu Shi, Lars G. Fritsche, Maxwell Salvatore, Andrew J. Admon +3 more

Characterizing and Predicting Post-Acute Sequelae of SARS CoV-2 infection (PASC) in a Large Academic Medical Center in the US

medRxiv(2022)10.1101/2022.10.21.22281356

Top 51%

0.344DataRank

Top 51%4 citations

Weijia Jin, Andrew J. Admon, Bhramar Mukherjee, Lars G. Fritsche

Estimating COVID-19 Vaccination and Booster Effectiveness Using Electronic Health Records From an Academic Medical Center in Michigan

AJPM Focus(2022)10.1016/j.focus.2022.100015

N/A

0.312DataRank · unranked

7 citations

Tian Gu, Abram L. Wagner, Bhramar Mukherjee, Lars G. Fritsche, Emily Roberts

Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT

medRxiv(2021)10.1101/2021.09.20.21262960

N/A

0.208DataRank · unranked

3 citations

Ailin Falkmo Hansen, Sarah E. Graham, Sarah A. Gagliano Taliun, Kuan-Han Wu, Wei Zhou +14 more

On Cross-ancestry Cancer Polygenic Risk Scores

medRxiv(2021)10.1101/2021.02.24.21252351

N/A

0.208DataRank · unranked

3 citations

Ying Ma, Daiwei Zhang, Maxwell Salvatore, Seunggeun Lee, Xiang Zhou +2 more

LabWAS: novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks

medRxiv(2020)10.1101/2020.04.08.19011478

Top 65%

0.196DataRank

Top 65%2 citations

Joshua S. Weinstock, Lisa A. Bastarache, Daniel B. Larach, Lars G. Fritsche, Ellen M. Schmidt +6 more

ExPRSweb - An Online Repository with Polygenic Risk Scores for Common Health-related Exposures

medRxiv(2022)10.1101/2022.01.13.22269176

Top 66%

0.183DataRank

Top 66%1 citations

Snehal Patil, Xiang Zhou, Bhramar Mukherjee, Lars G. Fritsche, Ying Ma

Incorporating functional annotation with bilevel continuous shrinkage for polygenic risk prediction

Research Square(2023)10.21203/rs.3.rs-2759690/v1

N/A

0.104DataRank · unranked

1 citations

Na Yeon Kim, Lars G. Fritsche, Bhramar Mukherjee, Seunggeun Lee, Yongwen Zhuang

To weight or not to weight? Studying the effect of selection bias in three large EHR-linked biobanks

medRxiv(2024)10.1101/2024.02.12.24302710

Top 78%

0.104DataRank

Top 78%1 citations

Ritoban Kundu, Xu Shi, Christopher R. Friese, Seunggeun Lee, Lars G. Fritsche +5 more

Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population

medRxiv(2020)10.1101/2020.09.04.20187401

N/A

0DataRank · unranked

0 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +22 more

Assessing the added value of linking electronic health records to improve the prediction of self-reported COVID-19 testing and diagnosis

PLoS ONE(2022)10.1371/journal.pone.0269017

N/A

0DataRank · unranked

2 citations

Jonathan Boss, Maxwell Salvatore, Jennifer A. Smith, Lars G. Fritsche, Bhramar Mukherjee +1 more

The Construction of Multi-ethnic Polygenic Risk Score using Transfer Learning

medRxiv(2022)10.1101/2022.03.08.22272114

N/A

0DataRank · unranked

7 citations

Lars G. Fritsche, Jennifer A. Smith, Bhramar Mukherjee, Seunggeun Lee, Zhangchen Zhao

The construction of cross-population polygenic risk scores using transfer learning

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.010

N/A

0DataRank · unranked

87 citations

Lars G. Fritsche, Jennifer A. Smith, Bhramar Mukherjee, Seunggeun Lee, Zhangchen Zhao

COVID-19 outcomes by cancer status, type, treatment, and vaccination

medRxiv(2022)10.1101/2022.04.19.22274047

N/A

0DataRank · unranked

0 citations

Miriam M. Hu, Lauren J. Beesley, Alison M. Mondul, Celeste Leigh Pearce, Christopher R. Friese +3 more

A Case-Crossover Phenome-wide Association Study (PheWAS) for Understanding Post-COVID-19 Diagnosis Patterns

medRxiv(2022)10.1101/2022.07.07.22277394

N/A

0DataRank · unranked

0 citations

Xu Shi, Chen Chen, Lars G. Fritsche, Bhramar Mukherjee, Spencer R. Haupert

Genome-wide association study of cardiac troponin I in the general population

Human Molecular Genetics(2021)10.1093/hmg/ddab124

N/A

0DataRank · unranked

20 citations

Helge Røsjø, Anne Richmond, Magnus Nakrem Lyngbakken, Sarah E. Graham, Ailin Falkmo Hansen +25 more

A Novel Variant in APOB Gene Causes Extremely Low LDL-C Without Known Adverse Effects

JACC Case Reports(2020)10.1016/j.jaccas.2020.03.016

N/A

0DataRank · unranked

2 citations

Whitney Hornsby, Linda Farhat, Melvyn Rubenfire, Lars G. Fritsche, Kristian Hveem +5 more

Phenotype risk scores (PheRS) for pancreatic cancer using time-stamped electronic health record data: Discovery and validation in two large biobanks

Journal of Biomedical Informatics(2020)10.1016/j.jbi.2020.103652

N/A

0DataRank · unranked

31 citations

Lauren J. Beesley, Lars G. Fritsche, David A. Hanauer, Xu Shi, Alison M. Mondul +3 more

Utility of family history in disease prediction in the era of polygenic scores

medRxiv(2021)10.1101/2021.06.25.21259158

N/A

0DataRank · unranked

1 citations

Ida Surakka, Sarah E. Graham, Jonas B. Nielsen, Wei Zhou, Maiken E. Gabrielsen +11 more

COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study

Osteoarthritis and Cartilage Open(2023)10.1016/j.ocarto.2023.100424

N/A

0DataRank · unranked

8 citations

Sigrid Børte, Lene Bjerke Laborie, Hege Kristiansen, Annette Schäfer, Amy E. Martinsen +25 more

Understanding the Patterns of Serological Testing for COVID-19 Pre- and Post-Vaccination Rollout in Michigan

Journal of Clinical Medicine(2021)10.3390/jcm10194341

N/A

0DataRank · unranked

4 citations

Stephen Salerno, Xu Shi, Seunggeun Lee, Bhramar Mukherjee, Lars G. Fritsche +1 more

Uncovering associations between pre-existing conditions and COVID-19 Severity: A polygenic risk score approach across three large biobanks

PLoS Genetics(2023)10.1371/journal.pgen.1010907

N/A

0DataRank · unranked

9 citations

Kisung Nam, Jiacong Du, Ritoban Kundu, Maxwell Salvatore, Xu Shi +4 more

Design and analysis heterogeneity in observational studies of COVID-19 booster effectiveness: A review and case study

Science Advances(2023)10.1126/sciadv.adj3747

N/A

0DataRank · unranked

4 citations

Xu Shi, Lars G. Fritsche, Maxwell Salvatore, Abram L. Wagner, Emily T. Martin +2 more

New insights into the genetic etiology of 57 essential and non-essential trace elements in humans

medRxiv(2023)10.1101/2023.04.25.23289097

N/A

0DataRank · unranked

4 citations

Ailin Falkmo Hansen, Brooke N. Wolford, Laurent F. Thomas, Humaira Rasheed, Anica Simić +19 more

Design and Analysis Heterogeneity in Observational Studies of COVID-19 Booster Effectiveness: A Review and Case Study

medRxiv(2023)10.1101/2023.06.22.23291692

N/A

0DataRank · unranked

0 citations

Xu Shi, Lars G. Fritsche, Maxwell Salvatore, Abram L. Wagner, Emily T. Martin +2 more

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Nature Communications(2020)10.1038/s41467-020-17315-0

N/A

0DataRank · unranked

37 citations

Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu +45 more

The Effect of Genetic Variants Associated With Age-Related Macular Degeneration Varies With Age

Investigative Ophthalmology & Visual Science(2020)10.1167/iovs.61.14.17

N/A

0DataRank · unranked

12 citations

Laura Lorés‐Motta, Lebriz Altay, Lars G. Fritsche, Anneke I. den Hollander, Sascha Fauser +1 more

Cluster Analysis and Genotype–Phenotype Assessment of Geographic Atrophy in Age-Related Macular Degeneration

Ophthalmology Retina(2021)10.1016/j.oret.2021.07.006

N/A

0DataRank · unranked

8 citations

Neal L. Oden, Elvira Agrón, Traci E. Clemons, Alice K. Henning, Lars G. Fritsche +3 more

Improving prediction models of amyotrophic lateral sclerosis (ALS) using polygenic, pre-existing conditions, and survey-based risk scores in the UK Biobank

Journal of Neurology(2024)10.1007/s00415-024-12644-2

N/A

0DataRank · unranked

5 citations

Jonathan Boss, Kelly M. Bakulski, Stephen A. Goutman, Eva L. Feldman, Lars G. Fritsche +2 more

Incorporating functional annotation with bilevel continuous shrinkage for polygenic risk prediction

BMC Bioinformatics(2024)10.1186/s12859-024-05664-2

N/A

0DataRank · unranked

3 citations

Na Yeon Kim, Lars G. Fritsche, Bhramar Mukherjee, Seunggeun Lee, Yongwen Zhuang

Assessing the Clinical Utility of Published Prostate Cancer Polygenic Risk Scores in a Large Biobank Data Set

European Urology Oncology(2024)10.1016/j.euo.2024.04.017

N/A

0DataRank · unranked

2 citations

Helen H. Sun, Udit Singhal, Fredrick R. Schumacher, Erika Trapl, Johnie Rose +9 more

Expanding biobank pharmacogenomics through machine learning calls of structural variation

Genetics(2025)10.1093/genetics/iyaf088

N/A

0DataRank · unranked

0 citations

Amy L. Pasternak, Lars G. Fritsche, Emily M. Bertucci, Snehal Patil, Michael Boehnke +5 more

Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2

iScience(2021)10.1016/j.isci.2021.103196

N/A

0DataRank · unranked

17 citations

Brooke N. Wolford, Haocheng Lu, Wenying Liang, Jinjian Sun, Wei Zhou +20 more

A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.016

N/A

0DataRank · unranked

17 citations

Peter VandeHaar, Lars G. Fritsche, Sebastian Zöllner, Michael Boehnke, Laura J. Scott +2 more

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Scientific Reports(2020)10.1038/s41598-020-58510-9

N/A

0DataRank · unranked

63 citations

Susette Lauwen, Christina Kiel, Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey +95 more

Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT

Communications Biology(2022)10.1038/s42003-022-03529-z

N/A

0DataRank · unranked

39 citations

Sarah E. Graham, Kuan-Han H. Wu, Ailin Falkmo Hansen, Sarah A. Gagliano Taliun, Wei Zhou +14 more

A Case-Crossover Phenome-wide association study (PheWAS) for understanding Post-COVID-19 diagnosis patterns

Journal of Biomedical Informatics(2022)10.1016/j.jbi.2022.104237

N/A

0DataRank · unranked

11 citations

Xu Shi, Chen Chen, Lars G. Fritsche, Bhramar Mukherjee, Spencer R. Haupert

Lars G. Fritsche

Indexed papers

Top data-sharing exemplar

Papers