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J. Ulirsch · SciRah

Researcher profile · Semantic Scholar

J. Ulirsch

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J. Ulirsch — researcher profile on SciRah

h-index: 35
Works: 74
Citations: 10K

Most-cited papers

FinnGen provides genetic insights from a well-phenotyped isolated population
M. Kurki, J. Karjalainen, P. Palta, Timo P. Sipilä +164 more
2023Nature3,914 citations Open access
Semantic Scholar
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
K. Aragam, T. Jiang, A. Goel, S. Kanoni +91 more
2021Nature Genetics639 citations Open access
Semantic Scholar
Genome-wide enhancer maps link risk variants to disease genes
Joseph Nasser, Drew T. Bergman, Charles P. Fulco, Philine Guckelberger +28 more
2021Nature569 citations Open access
Semantic Scholar
Lineage Tracing In Humans Enabled By Mitochondrial Mutations And Single Cell Genomics
Leif S. Ludwig, C. Lareau, J. Ulirsch, Elena Christian +16 more
2019Cell493 citations Open access
Semantic Scholar
Functionally-informed fine-mapping and polygenic localization of complex trait heritability
Omer Weissbrod, Farhad Hormozdiari, C. Benner, Ran Cui +10 more
2019Nature Genetics366 citations Open access
Semantic Scholar
The NORAD lncRNA assembles a topoisomerase complex critical for genome stability
M. Munschauer, Celina T. Nguyen, Klára Sirokmán, Christina R. Hartigan +10 more
2018Nature340 citations Open access
Semantic Scholar
Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases
Elle M. Weeks, J. Ulirsch, Nathan Cheng, Brian L. Trippe +23 more
2020Nature Genetics331 citations Open access
Semantic Scholar
A cross-disorder dosage sensitivity map of the human genome
Ryan L. Collins, J. Glessner, E. Porcu, Theodore J. Morley +30 more
2021medRxiv327 citations Open access
Semantic Scholar
Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits
J. Ulirsch, Satish K. Nandakumar, Li Wang, Felix C Giani +7 more
2016Cell320 citations Open access
Semantic Scholar
Genetic predisposition to mosaic Y chromosome loss in blood
D. Thompson, G. Genovese, J. Halvardson, J. Ulirsch +57 more
2019Nature307 citations Open access
Semantic Scholar
The Genetic Landscape of Diamond-Blackfan Anemia
J. Ulirsch, J. M. Verboon, S. Kazerounian, Michael H. Guo +38 more
2018bioRxiv231 citations Open access
Semantic Scholar
Interrogation of human hematopoiesis at single-cell and single-variant resolution
J. Ulirsch, C. Lareau, Erik L. Bao, Leif S. Ludwig +10 more
2018Nature Genetics190 citations Open access
Semantic Scholar
Genome-wide functional screen of 3’UTR variants uncovers causal variants for human disease and evolution
Dustin Griesemer, James R. Xue, S. Reilly, J. Ulirsch +12 more
2021bioRxiv143 citations Open access
Semantic Scholar
Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis
Leif S. Ludwig, C. Lareau, Erik L. Bao, Satish K. Nandakumar +9 more
2019Cell Reports143 citations Open access
Semantic Scholar
BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations.
Anindita Basak, M. Hančárová, J. Ulirsch, T. Balci +11 more
2015Journal of Clinical Investigation143 citations Open access
Semantic Scholar
Tractor uses local ancestry to enable inclusion of admixed individuals into GWAS and boost power
E. Atkinson, A. Maihofer, M. Kanai, Alicia R. Martin +10 more
2021Nature Genetics140 citations Open access
Semantic Scholar
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation
A. R. Kim, J. Ulirsch, S. Wilmes, E. Unal +17 more
2017Cell104 citations Open access
Semantic Scholar
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation
Anindita Basak, M. Munschauer, C. Lareau, Kara E Montbleau +17 more
2020Nature Genetics97 citations Open access
Semantic Scholar
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
M. Kurki, J. Karjalainen, P. Palta, Timo P. Sipilä +164 more
2023Nature95 citations Open access
Semantic Scholar
Incidence and Predictors of Neck and Widespread Pain after Motor Vehicle Collision among US Litigants and Non-Litigants
S. Mclean, J. Ulirsch, G. Slade, A. Soward +9 more
2013Pain95 citations Open access
Semantic Scholar
Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs
Qing-Bo S. Wang, David R. Kelley, J. Ulirsch, M. Kanai +33 more
2020Nature Communications91 citations Open access
Semantic Scholar
Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells
Felix C Giani, Claudia Fiorini, Aoi Wakabayashi, Leif S. Ludwig +17 more
2015Cell Stem Cell89 citations Open access
Semantic Scholar
Pain and somatic symptoms are sequelae of sexual assault: Results of a prospective longitudinal study
J. Ulirsch, L. Ballina, A. Soward, C. Rossi +8 more
2014European Journal of Pain88 citations
Semantic Scholar
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
L. Raffield, J. Ulirsch, Rakhi P. Naik, Samuel Lessard +21 more
2018PLoS Genetics71 citations Open access
Semantic Scholar
Polymorphisms in the glucocorticoid receptor co-chaperone FKBP5 predict persistent musculoskeletal pain after traumatic stress exposure
A. Bortsov, Jennifer E. Smith, L. Diatchenko, A. Soward +14 more
2013Pain71 citations Open access
Semantic Scholar
Detecting genome-wide directional effects of transcription factor binding on polygenic disease risk
Yakir A. Reshef, H. Finucane, David R. Kelley, Alexander Gusev +15 more
2017Nature Genetics68 citations Open access
Semantic Scholar
Improving fine-mapping by modeling infinitesimal effects
Ran Cui, Roy A. Elzur, M. Kanai, J. Ulirsch +5 more
2023bioRxiv67 citations Open access
Semantic Scholar
Direct characterization of cis-regulatory elements and functional dissection of complex genetic associations using HCR-FlowFISH
S. Reilly, Sager J. Gosai, A. Gutierrez, Ava Mackay-Smith +12 more
2021Nature Genetics67 citations Open access
Semantic Scholar
No Man is an Island: living in a disadvantaged neighborhood influences chronic pain development after motor vehicle collision, and this effect is moderated by common genetic variation influencing HPA axis function
J. Ulirsch, M. Weaver, A. Bortsov, A. Soward +8 more
2014Pain65 citations Open access
Semantic Scholar
Insight into GATA1 transcriptional activity through interrogation of cis elements disrupted in human erythroid disorders
Aoi Wakabayashi, J. Ulirsch, Leif S. Ludwig, Claudia Fiorini +5 more
2016Proceedings of the National Academy of Sciences of the United States of America61 citations Open access
Semantic Scholar
Vimentin DNA methylation predicts survival in breast cancer
J. Ulirsch, Cheng Fan, G. Knafl, Ming J. Wu +3 more
2012Breast Cancer Research and Treatment60 citations Open access
Semantic Scholar
HRI coordinates translation necessary for protein homeostasis and mitochondrial function in erythropoiesis
Shu-Ping Zhang, Alejandra Macias-Garcia, J. Ulirsch, J. Velazquez +4 more
2019eLife59 citations Open access
Semantic Scholar
Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features
John P. Ray, Carl G. de Boer, Charles P. Fulco, C. Lareau +12 more
2020Nature Communications55 citations Open access
Semantic Scholar
Altered Chromatin Occupancy of Master Regulators Underlies Evolutionary Divergence in the Transcriptional Landscape of Erythroid Differentiation
J. Ulirsch, J. Lacy, X. An, N. Mohandas +2 more
2014PLoS Genetics49 citations Open access
Semantic Scholar
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms
Michael H. Guo, Satish K. Nandakumar, J. Ulirsch, S. Zekavat +18 more
2016Proceedings of the National Academy of Sciences of the United States of America38 citations Open access
Semantic Scholar
Functional characterization of T2D-associated SNP effects on baseline and ER stress-responsive β cell transcriptional activation
Shubham Khetan, S. Kales, R. Kursawe, Alexandria Jillette +5 more
2021Nature Communications35 citations Open access
Semantic Scholar
Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation
Nour J Abdulhay, Claudia Fiorini, J. M. Verboon, Leif S. Ludwig +16 more
2019Journal of Experimental Medicine32 citations Open access
Semantic Scholar
Inducible Gata1 suppression expands megakaryocyte-erythroid progenitors from embryonic stem cells.
J. Noh, Shilpa Gandre-Babbe, Yuhuan Wang, V. Hayes +13 more
2015Journal of Clinical Investigation31 citations Open access
Semantic Scholar
Developmentally-Faithful and Effective Human Erythropoiesis in Immunodeficient and Kit Mutant Mice
Claudia Fiorini, Nour J Abdulhay, Sean Mcfarland, M. Munschauer +3 more
2017American journal of hematology/oncology27 citations Open access
Semantic Scholar
μ-Opioid receptor gene A118G polymorphism predicts pain recovery after sexual assault.
L. Ballina, J. Ulirsch, A. Soward, C. Rossi +9 more
2013Journal of Pain25 citations Open access
Semantic Scholar
A Congenital Anemia Reveals Distinct Targeting Mechanisms for Master Transcription Factor GATA1.
Leif S. Ludwig, C. Lareau, Erik L. Bao, Nan Liu +28 more
2022Blood24 citations Open access
Semantic Scholar
The Genetic Landscape of Diamond-Blackfan Anemia.
J. Ulirsch, J. M. Verboon, S. Kazerounian, Michael H. Guo +38 more
2019American Journal of Human Genetics24 citations Open access
Semantic Scholar
RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation
Danya J. Martell, Hope E. Merens, A. Caulier, Claudia Fiorini +14 more
2023Developmental Cell20 citations Open access
Semantic Scholar
Publisher Correction: The NORAD lncRNA assembles a topoisomerase complex critical for genome stability
M. Munschauer, Celina T. Nguyen, Klára Sirokmán, Christina R. Hartigan +10 more
2018Nature20 citations Open access
Semantic Scholar
Gene-centric functional dissection of human genetic variation uncovers regulators of hematopoiesis
Satish K. Nandakumar, Sean Mcfarland, L. M. Mateyka, C. Lareau +12 more
2018bioRxiv19 citations Open access
Semantic Scholar
Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia
O. Steinberg-Shemer, J. Ulirsch, S. Noy-Lotan, T. Krasnov +5 more
2017Cold Spring Harbor molecular case studies19 citations Open access
Semantic Scholar
Association of Epidemiologic Factors and Genetic Variants Influencing HPA Axis Function with Post-Concussive Symptoms after Minor Motor Vehicle Collision
Lauriane Auvergne, A. Bortsov, J. Ulirsch, D. Peak +7 more
2016Psychosomatic Medicine19 citations Open access
Semantic Scholar
Genome-wide maps of enhancer regulation connect risk variants to disease genes
Joseph Nasser, Drew T. Bergman, Charles P. Fulco, Philine Guckelberger +26 more
2020bioRxiv14 citations Open access
Semantic Scholar
Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia
J. Lacy, J. Ulirsch, R. Grace, Meghan C. Towne +5 more
2016Cold Spring Harbor molecular case studies13 citations Open access
Semantic Scholar
Confounding in ex vivo models of Diamond-Blackfan anemia.
J. Ulirsch, C. Lareau, Leif S. Ludwig, N. Mohandas +2 more
2017Blood9 citations Open access
Semantic Scholar

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