Joseph Glessner

Also affiliated with University of Pennsylvania

Biochemistry, Genetics and Molecular BiologyNeuroscience

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

4.7Author DataRank

Indexed papers

2in 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 2 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 48 papers — median percentile 48. Top paper: “Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains”.

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

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 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

A cross-disorder dosage sensitivity map of the human genome

medRxiv(2021)10.1101/2021.01.26.21250098

N/A

2.0DataRank · unranked

54 citations

Joseph Glessner, Eleonora Porcu, Lisa‐Marie Niestroj, Jacob C. Ulirsch, Georgios Kellaris +28 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

Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

Circulation(2021)10.1161/circulationaha.121.055562

N/A

1.2DataRank · unranked

49 citations

Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric Farber‐Eger +46 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

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Genome Research(2007)10.1101/gr.6861907

N/A

1.1DataRank · unranked

1896 citations

Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F.A. Grant +5 more

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

Genome biology(2024)10.1186/s13059-023-03136-z

N/A

0.629DataRank · unranked

16 citations

Rachel L. Kember, Anna Ulrich, Zhanna Balkhiyarova, Akram Alyass, Izzuddin M. Aris +95 more

Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

Arthritis & Rheumatology(2022)10.1002/art.42129

N/A

0.372DataRank · unranked

9 citations

Leslie A. Lange, Joseph Glessner, Jie Yang, Michael March, Charlly Kao +23 more

Clinical associations with a polygenic predisposition to benign lower white blood cell counts

Nature Communications(2024)10.1038/s41467-024-47804-5

N/A

0.312DataRank · unranked

7 citations

John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng +23 more

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Cell Reports(2021)10.1016/j.celrep.2021.110020

N/A

0DataRank · unranked

47 citations

Jennifer Nguyen, Timothy D. Arthur, Hiroko Matsui, Agnieszka D’Antonio‐Chronowska, Kelly A. Frazer +85 more

Genetic correlations between COVID-19 and a variety of traits and diseases

The Innovation(2021)10.1016/j.xinn.2021.100112

N/A

0DataRank · unranked

12 citations

Yun Li, Kenny Nguyen, Hui‐Qi Qu, Yichuan Liu, Joseph Glessner +3 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

Genetic architecture of asthma in African American patients

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.09.001

N/A

0DataRank · unranked

31 citations

Michael March, Frank Mentch, Hui‐Qi Qu, Yichuan Liu, Joseph Glessner +3 more

Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans

iScience(2022)10.1016/j.isci.2022.104650

N/A

0DataRank · unranked

11 citations

Joseph Glessner, Jingchun Qu, Steven Gilhool, Frank Mentch, Ian M. Campbell +4 more

Identification of Mitochondrial DNA Variants Associated With Risk of Neuroblastoma

JNCI Journal of the National Cancer Institute(2022)10.1093/jnci/djac012

N/A

0DataRank · unranked

10 citations

Yichuan Liu, Joseph Glessner, Cuiping Hou, Hui‐Qi Qu, Kenny Nguyen +6 more

Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing

Biomarker Research(2022)10.1186/s40364-022-00431-y

N/A

0DataRank · unranked

8 citations

Hui‐Qi Qu, Xiao Chang, Frank Mentch, Haijun Qiu, Kenny Nguyen +6 more

Trans-ethnic Genomic Informed Risk Assessment for Alzheimer’s disease: An International Hundred K+ Cohorts Consortium Study

medRxiv(2022)10.1101/2022.12.22.22283738

N/A

0DataRank · unranked

1 citations

Hui‐Qi Qu, John J. Connolly, Frank Mentch, Alexandre C. Pereira, Paulo A. Lotufo +19 more

Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes

Journal of Hepatology(2023)10.1016/j.jhep.2023.07.039

N/A

0DataRank · unranked

31 citations

Mylarappa Ningappa, Kim A. Ngo, Maliha Zahid, Juhoon So, Brandon W. Higgs +30 more

A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder–Associated Copy Number Variations

Biological Psychiatry(2023)10.1016/j.biopsych.2023.10.011

N/A

0DataRank · unranked

4 citations

Hui‐Qi Qu, Yichuan Liu, Joseph Glessner, Håkon Håkonarson, Xiao Chang

Trans‐ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study

Alzheimer s & Dementia(2023)10.1002/alz.13378

N/A

0DataRank · unranked

8 citations

Hui‐Qi Qu, John J. Connolly, Frank Mentch, Alexandre C. Pereira, Paulo A. Lotufo +19 more

The molecular genetic landscape of human brain size variation

Cell Reports(2023)10.1016/j.celrep.2023.113439

N/A

0DataRank · unranked

6 citations

Travis T. Mallard, Jacob W. Vogel, Young A Lee, Varun Warrier, Gareth Ball +19 more

TOPORS as a novel causal gene for Joubert syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63303

N/A

0DataRank · unranked

6 citations

Hui‐Qi Qu, Sinéad Cullina, Morgan L. McManus, Elaine H. Zackai, Joseph Glessner +3 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0DataRank · unranked

7 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development

Molecular Cancer(2023)10.1186/s12943-023-01828-5

N/A

0DataRank · unranked

1 citations

Hui‐Qi Qu, Xiao Chang, Frank Mentch, Haijun Qiu, Xiang Wang +5 more

High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations

Translational research(2023)10.1016/j.trsl.2023.11.004

N/A

0DataRank · unranked

1 citations

Joseph Glessner, Jingchun Qu, Yichuan Liu, Deborah Watson, Xiao Chang +6 more

High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCs

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.26.546614

N/A

0DataRank · unranked

4 citations

Jonathan E. Perdomo, Munir E. Khan, Brianna Disanza, Gregory G. Cajka, Sunyimeng Lei +12 more

KOLF2.1J iPSCs carry CNVs associated with neurodevelopmental disorders

Cell stem cell(2024)10.1016/j.stem.2024.02.007

N/A

0DataRank · unranked

18 citations

Jonathan E. Perdomo, Munir E. Khan, Thomas Roulé, Brianna Disanza, Gregory G. Cajka +12 more

Identification of genetic variants associated with clinical features of sickle cell disease

Scientific Reports(2024)10.1038/s41598-024-70922-5

N/A

0DataRank · unranked

5 citations

Xiao Chang, Frank Mentch, Kim Smith‐Whitley, Anita Bhandari, Cindy Norris +3 more

The copy number variant architecture of psychopathology and cognitive development in the ABCD ® study

medRxiv(2024)10.1101/2024.05.14.24307376

N/A

0DataRank · unranked

2 citations

Kevin Y. Sun, Benjamin Jung, Ran Barzilay, Tyler M. Moore, Laura Almasy +8 more

Copy number variations contribute to malignant tumor development in children with serious birth defects

Molecular Oncology(2024)10.1002/1878-0261.13718

N/A

0DataRank · unranked

0 citations

Joseph Glessner, Hui‐Qi Qu, Xiao Chang, Haijun Qiu, Tiancheng Wang +3 more

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

UNC Libraries(2024)10.17615/c75g-gz70

N/A

0DataRank · unranked

0 citations

Maties Torrent, Struan F.A. Grant, Jonathan A. Mitchell, Joseph M. Kindler, Emily Oken +95 more

Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis

Nature Communications(2025)10.1038/s41467-025-58310-7

N/A

0DataRank · unranked

13 citations

Mrinal K. Sarkar, Michael March, Amir Hossein Saeidian, Frank Mentch, Chen-Lin Hsieh +16 more

Developing Predictive Models for Periodontitis Progression Using Artificial Intelligence: A Longitudinal Cohort Study

Journal Of Clinical Periodontology(2025)10.1111/jcpe.14194

N/A

0DataRank · unranked

12 citations

Lannawill Caruth, Ganesh Chandrasekaran, Andrew J. Cucchiara, Michael J. Kallan, Lynn Martin +9 more

Genome-wide association study and HLA genotyping for beryllium disease susceptibility in a European descent population

Gene(2025)10.1016/j.gene.2025.149820

N/A

0DataRank · unranked

1 citations

Tasha E. Fingerlin, Sean Jacobson, Margaret M. Mroz, Kenneth D. Rosenman, Milton D. Rossman +10 more

Genetic analysis of two bladder exstrophy populations of South Asian and North American origin

Journal of Pediatric Urology(2025)10.1016/j.jpurol.2025.04.018

N/A

0DataRank · unranked

1 citations

Dana Weiß, Austin Thompson, Rakesh Joshi, Jaishri Ramji, Aseem R. Shukla +10 more

Deep learning algorithms reveal genomic markers for anxiety disorder in a large cohort of children with down syndrome

Molecular Psychiatry(2025)10.1038/s41380-025-03065-2

N/A

0DataRank · unranked

1 citations

Hui‐Qi Qu, Xiao Chang, Frank Mentch, Haijun Qiu, Shahram Torkamandi +6 more

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Nature Communications(2020)10.1038/s41467-019-13624-1

N/A

0DataRank · unranked

87 citations

Joseph Glessner, Bradley P. Coe, Jin Li, Maedeh Mohebnasab, Xiao Chang +36 more

Common genetic variants on 5p14.1 associate with autism spectrum disorders

UNC Libraries(2020)10.17615/g04w-kk07

N/A

0DataRank · unranked

63 citations

Ami Klin, Rosetta Chiavacci, Cuiping Hou, Hongmei Dong, Lisa I. Sonnenblick +27 more

Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans

Translational Psychiatry(2020)10.1038/s41398-020-01064-1

N/A

0DataRank · unranked

19 citations

Yichuan Liu, Frank Mentch, Joseph Glessner, Hui‐Qi Qu, Kenny Nguyen +3 more

Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma

JNCI Journal of the National Cancer Institute(2020)10.1093/jnci/djaa024

N/A

0DataRank · unranked

11 citations

Marina Bakay, Yichuan Liu, Joseph Glessner, Komal S. Rathi, Cuiping Hou +8 more

Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality

Frontiers in Physiology(2020)10.3389/fphys.2020.538701

N/A

0DataRank · unranked

26 citations

Mylarappa Ningappa, Joseph Glessner, Jun Min, Chethan Ashokkumar, Sarangarajan Ranganathan +29 more

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

UNC Libraries(2020)10.17615/a03d-0d18

N/A

0DataRank · unranked

1 citations

Daniel L. Dries, Kiang Liu, Xiaofeng Zhu, Charleston W. K. Chiang, Adebowale Adeyemo +27 more

Machine learning reduced gene/non-coding RNA features that classify Schizophrenia patients accurately and highlight insightful gene clusters

medRxiv(2020)10.1101/2020.06.08.20125906

N/A

0DataRank · unranked

2 citations

Hui‐Qi Qu, Xiao Chang, Lifeng Tian, Joseph Glessner, Patrick Sleiman +2 more

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

UNC Libraries(2020)10.17615/dvnt-qn64

N/A

0DataRank · unranked

0 citations

Dexter Hadley, Mingyao Li, Ingrid Lindquist, Brett S. Abrahams, Edward I. Herman +27 more

The landscape of recombination in African Americans

UNC Libraries(2020)10.17615/hgd9-hc10

N/A

0DataRank · unranked

0 citations

W. Ryan Diver, Sarah G. Buxbaum, Sue A. Ingles, Sonja I. Berndt, Boerwinkle, Eric +27 more

Individual common variants exert weak effects on the risk for autism spectrum disorders

UNC Libraries(2020)10.17615/8394-9h82

Top 100%

0DataRank

Top 100%0 citations

Emily L. Crawford, Joseph Glessner, John R. Gilbert, Nadia Bolshakova, Gillberg, Christopher +27 more

Joseph Glessner

Indexed papers

Top data-sharing exemplar

Papers