Lili Milani

Biochemistry, Genetics and Molecular BiologyMedicine

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

10.1Author DataRank

Indexed papers

6in 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 6 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 cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Papers

Driven by 50 papers — median percentile 84. Top paper: “Rare coding variants in ten genes confer substantial risk for schizophrenia”.

Rare coding variants in ten genes confer substantial risk for schizophrenia

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

N/A

7.2DataRank · unranked

900 citations

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

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

Genome biology(2021)10.1186/s13059-021-02398-9

N/A

5.8DataRank · unranked

307 citations

Josine L. Min, Rebecca Richmond, Ake T. Lu, Maria Sobczyk, Gail Davies +95 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

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational study

The Lancet Public Health(2022)10.1016/s2468-2667(22)00042-1

N/A

4.6DataRank · unranked

169 citations

Anikó Lovik, Anna Bára Unnarsdóttir, Daniel L. McCartney, Helga Ask, Kadri Kõiv +44 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

Resource profile and user guide of the Polygenic Index Repository

Nature Human Behaviour(2021)10.1038/s41562-021-01119-3

Top 7%

3.0DataRank

Top 7%184 citations

Casper A.P. Burik, Grant Goldman, Nancy Wang, Hariharan Jayashankar, Michael Bennett +60 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

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

Nature Communications(2020)10.1038/s41467-020-17002-0

N/A

2.1DataRank · unranked

76 citations

Pamela M. Rist, Iyas Daghlas, Franco Giulianini, Padhraig Gormley, Verneri Anttila +95 more

Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.008

N/A

1.7DataRank · unranked

56 citations

Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson +64 more

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.010

N/A

1.6DataRank · unranked

76 citations

Maxim B. Freidin, Linda Broer, Berthe C. Oosterloo, Shuyang Yao, Yitian Zhou +65 more

Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure

Hypertension(2020)10.1161/hypertensionaha.120.14973

N/A

1.4DataRank · unranked

87 citations

Miina Ollikainen, Maheswary Muniandy, Tao Zhang, Jenny van Dongen, Guang Hao +47 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

Psychiatric disorders and subsequent risk of cardiovascular disease: a longitudinal matched cohort study across three countries

EClinicalMedicine(2023)10.1016/j.eclinm.2023.102063

Top 16%

1.3DataRank

Top 16%62 citations

Dorte Helenius Mikkelsen, Laura Birgit Luitva, Huan Song, Silva Kasela, Thor Aspelund +13 more

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Nature Human Behaviour(2023)10.1038/s41562-023-01528-6

N/A

1.3DataRank · unranked

59 citations

Felix R. Day, Nicola Barban, Felix C. Tropf, David M. Brazel, Diana van Heemst +92 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

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Nature Communications(2023)10.1038/s41467-023-36862-w

N/A

1.1DataRank · unranked

56 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +81 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

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

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0.665DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 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

Characterising the genetic architecture of changes in adiposity during adulthood using electronic health records

Nature Communications(2024)10.1038/s41467-024-49998-0

Top 30%

0.656DataRank

Top 30%19 citations

Habib Ganjgahi, Duncan S. Palmer, Kayesha Coley, Gregorio V. Linchangco, Qin Hui +19 more

GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets

Nature Communications(2025)10.1038/s41467-025-56719-8

N/A

0.631DataRank · unranked

66 citations

Philip E. Stuart, John Bowes, David Ellinghaus, Joanne Nititham, Jake Saklatvala +89 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

Genome-wide association study identifies five risk loci for pernicious anemia

Nature Communications(2021)10.1038/s41467-021-24051-6

N/A

0.596DataRank · unranked

52 citations

Maarja Lepamets, Mariann Koel, Erik Abner, Andres Metspalu, Mari Nelis +4 more

Genetic drivers and cellular selection of female mosaic X chromosome loss

Nature(2024)10.1038/s41586-024-07533-7

N/A

0.574DataRank · unranked

45 citations

Giulio Genovese, Yajie Zhao, Matti Pirinen, Seyedeh M. Zekavat, Katherine A. Kentistou +95 more

Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.12824

N/A

0.571DataRank · unranked

19 citations

Aïcha Soumaré, Joshua C. Bis, Ida Surakka, Tuuli Jürgenson, Pierre Joly +29 more

Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse

Nature Communications(2022)10.1038/s41467-022-31188-5

N/A

0.538DataRank · unranked

35 citations

Kristi Läll, Maarja Lepamets, Andres Metspalu, Mari Nelis, Lili Milani +8 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Molecular Psychiatry(2021)10.1038/s41380-021-01087-0

N/A

0.483DataRank · unranked

24 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02156-8

N/A

0.464DataRank · unranked

21 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +57 more

Recommendations for defining treatment outcomes in major psychiatric disorders using real-world data

The Lancet Psychiatry(2025)10.1016/s2215-0366(25)00061-6

N/A

0.406DataRank · unranked

14 citations

Sophie E. Smart, Guðmundur Einarsson, Anders Kämpe, Lina Jönsson, Maris Alver +25 more

Resource Profile and User Guide of the Polygenic Index Repository

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.08.443158

Top 52%

0.336DataRank

Top 52%5 citations

Casper A.P. Burik, Grant Goldman, Nancy Wang, Hariharan Jayashankar, Michael Bennett +37 more

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

medRxiv(2024)10.1101/2024.07.13.24310361

N/A

0.312DataRank · unranked

7 citations

Tuuli Jürgenson, Guðmundur Einarsson, Brittany L. Mitchell, Arvid Harder, Luis M. García‐Marín +18 more

Genome-wide meta-analyses of non-response to antidepressants identify novel loci and potential drugs

Research Square(2024)10.21203/rs.3.rs-5418279/v1

N/A

0.277DataRank · unranked

4 citations

Tuuli Jürgenson, Guðmundur Einarsson, Brittany L. Mitchell, Arvid Harder, Luis M. García‐Marín +21 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

0.241DataRank · unranked

4 citations

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

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.123505

N/A

0.208DataRank · unranked

3 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

Critical Care Explorations(2023)10.1097/cce.0000000000000997

N/A

0.104DataRank · unranked

1 citations

Garen Manvelian, Alida Coppi, Amy Damask, Michael Cantor, Manuel A. R. Ferreira +35 more

Mechanistic endotyping of the ROS/cGMP disease cluster in the Estonian Biobank

Mechanistic endotyping of the ROS/cGMP disease cluster in the Estonian Biobank10.58647/rexpo.23000033.v1

N/A

0DataRank · unranked

0 citations

Jaanika Kronberg, Alexandra Petraina, Mayra Pacheco Pachado, Mari Nelis, Lili Milani +5 more

Genetic and Functional Characterization of ANGPTL7 as a Therapeutic Target for Glaucoma

Research Square(2021)10.21203/rs.3.rs-858876/v1

N/A

0DataRank · unranked

0 citations

Gaurang Patel, Lauren Gurski, Ariane Ayer, Trikaladarshi Persaud, Matthew Still +49 more

Differences in local population history at the finest level: the case of the Estonian population

European Journal of Human Genetics(2020)10.1038/s41431-020-0699-4

N/A

0DataRank · unranked

83 citations

Francesco Montinaro, Alena Kushniarevich, Georgi Hudjashov, Flora Jay, Lauri Saag +16 more

Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics

Science Translational Medicine(2020)10.1126/scitranslmed.aay6570

N/A

0DataRank · unranked

117 citations

Kristi Krebs, Chia‐Yen Chen, Ruth Boxall, Jenny C. Censin, Teresa Ferreira +15 more

Targeted profiling of 5-(hydroxy)methylcytosine in genomic DNA from human livers: Next-generation sequencing of target enriched DNA reveals unexpectedly high interindividual variability of cytosine methylation and hydroxymethylation

2014 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)(2014)10.1109/bibm.2014.6999389

N/A

0DataRank · unranked

0 citations

Magnus Ingelman-Sundberg, Mart Kals, Lili Milani, Maxim Ivanov

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

N/A

0DataRank · unranked

0 citations

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

HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases

Communications Biology(2023)10.1038/s42003-023-05496-5

N/A

0DataRank · unranked

33 citations

Joseph Farjoun, Tomoko Nakanishi, Tianyuan Lu, Erik Abner, Yiheng Chen +17 more

HLA allele-calling using whole-exome sequencing identifies 129 novel associations in 11 autoimmune diseases: a multi-ancestry analysis in the UK Biobank

medRxiv(2023)10.1101/2023.01.15.23284570

N/A

0DataRank · unranked

1 citations

Yossi Farjoun, Tomoko Nakanishi, Tianyuan Lu, Erik Abner, Yiheng Chen +17 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

UNC Libraries(2024)10.17615/9849-hx54

N/A

0DataRank · unranked

0 citations

M. FORNAGE, J.I. Rotter, Michael R. Brown, L.-P. Lyytikäinen, B. Kühnel +95 more

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

UNC Libraries(2024)10.17615/fg4z-2k83

N/A

0DataRank · unranked

0 citations

L. C. M., André Goedegebure, Antti Mäkitie, Sullivan P.F, Shaohua Yao +62 more

Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architecture

medRxiv(2025)10.1101/2025.07.16.25331639

N/A

0DataRank · unranked

1 citations

Piotr Jahołkowski, Alexey Shadrin, Elise Koch, Laura Birgit Luitva, Dorte Helenius Mikkelsen +27 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

Lili Milani

Indexed papers

Top data-sharing exemplar

Papers