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Author Details

Krzysztof Kiryluk
Columbia University
2006
156
44
PMIDPaper TitleJournal TitlePublished Year
36302597Genomic Disorders in CKD across the Lifespan.J Am Soc Nephrol2023
36309125On the way to translate GWAS into kidney disease mechanisms.Kidney Int2023
36302597Genomic Disorders in CKD across the Lifespan.J Am Soc Nephrol2023
37746849Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.Genet Med2023
37689782Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.Nat Commun2023
37471101Anti-PLA2R Antibody Levels and Clinical Risk Factors for Treatment Nonresponse in Membranous Nephropathy.Clin J Am Soc Nephrol2023
37214819Polygenic risk affects the penetrance of monogenic kidney disease.medRxiv2023
37337107Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.Nat Genet2023
37333123The chromatin landscape of healthy and injured cell types in the human kidney.bioRxiv2023
36758113Clinical and Genetic Characteristics of CKD Patients with High-Risk APOL1 Genotypes.J Am Soc Nephrol2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
37120605Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.Nat Commun2023
36995132Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.J Am Soc Nephrol2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37181728A metadata framework for computational phenotypes.JAMIA Open2023
36737471Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.Sci Rep2023
37169873CARMA is a new Bayesian model for fine-mapping in genome-wide association meta-analyses.Nat Genet2023
37227924Global Incidence of IgA Nephropathy by Race and Ethnicity: A Systematic Review.Kidney3602023
36782330BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data.Genome Biol2023
37746849Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.Genet Med2023
37689782Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.Nat Commun2023
37120605Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.Nat Commun2023
37214819Polygenic risk affects the penetrance of monogenic kidney disease.medRxiv2023
37181728A metadata framework for computational phenotypes.JAMIA Open2023
37337107Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.Nat Genet2023
37169873CARMA is a new Bayesian model for fine-mapping in genome-wide association meta-analyses.Nat Genet2023
37333123The chromatin landscape of healthy and injured cell types in the human kidney.bioRxiv2023
37227924Global Incidence of IgA Nephropathy by Race and Ethnicity: A Systematic Review.Kidney3602023
37471101Anti-PLA2R Antibody Levels and Clinical Risk Factors for Treatment Nonresponse in Membranous Nephropathy.Clin J Am Soc Nephrol2023
36995132Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.J Am Soc Nephrol2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36782330BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data.Genome Biol2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
36737471Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.Sci Rep2023
36758113Clinical and Genetic Characteristics of CKD Patients with High-Risk APOL1 Genotypes.J Am Soc Nephrol2023
36309125On the way to translate GWAS into kidney disease mechanisms.Kidney Int2023
33993232Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis.Rheumatology (Oxford)2022
35595084Multiancestral polygenic risk score for pediatric asthma.J Allergy Clin Immunol2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35450416Clinical Predictors and Prognosis of Recurrent IgA Nephropathy in the Kidney Allograft.Glomerular Dis2022
35765100Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.Genome Med2022
36161695Incorporating genetics services into adult kidney disease care.Am J Med Genet C Semin Med Genet2022
35618394Glomerular Diseases of the Kidney Allograft: Toward a Precision Medicine Approach.Semin Nephrol2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36062073Cystatin C is associated with adverse COVID-19 outcomes in diverse populations.iScience2022
35988936Kidney disease progression and collider bias in GWAS.Kidney Int2022
36531879Clinicopathologic Significance of Predominant Lambda Light Chain Deposition in IgA Nephropathy.Kidney Int Rep2022
33993232Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis.Rheumatology (Oxford)2022
33818625IgA vasculitis with nephritis: update of pathogenesis with clinical implications.Pediatr Nephrol2022
34571062Improving Clinical Trials for Anticomplement Therapies in Complement-Mediated Glomerulopathies: Report of a Scientific Workshop Sponsored by the National Kidney Foundation.Am J Kidney Dis2022
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Collaborators

Ali G Gharavi
Columbia University College of Physicians and Surgeons
Co-authored papers 71
Vivette D D'Agati
Columbia University Irving Medical Center
Co-authored papers 18
Maddalena Marasa
Columbia University College of Physicians and Surgeons
Co-authored papers 18
Nan Chen
Co-authored papers 15
Ning Shang
Columbia University Irving Medical Center
Co-authored papers 15
Chunhua Weng
Columbia University Irving Medical Center
Co-authored papers 15
Richard P Lifton
The Rockefeller University
Co-authored papers 13
Sumit Mohan
Vagelos College of Physicians and Surgeons, Columbia University
Co-authored papers 12
Matthew G Sampson
Co-authored papers 11
George Hripcsak
Columbia University
Co-authored papers 11
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 11
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
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Guillaume Butler-Laporte
McGill University
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Iftikhar J Kullo
Mayo Clinic
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David R Crosslin
University of Washington Medical Center
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Jordan G Nestor
Columbia University
Co-authored papers 9
Eimear E Kenny
Icahn School of Medicine at Mount Sinai, NY Institute for Genomic Health
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David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 9
Elizabeth W Karlson
Brigham and Women's Hospital
Co-authored papers 8
Hila Milo Rasouly
Center for Precision Medicine and Genomics, Columbia University Irving Medical Center
Co-authored papers 8
Bahram Namjou
Cincinnati Children's Hospital
Co-authored papers 8
Daniele Cusi
Institute of Biomedical Technologies, National Research Council of Italy
Co-authored papers 8
Ruth J F Loos
Co-authored papers 8
John Brent Richards
Lady Davis Institute for Medical Research, Jewish General Hospital
Co-authored papers 8
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 8
Gundula Povysil
Institute for Genomic Medicine, Columbia University Medical Center
Co-authored papers 8
Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 7
Zina Moldoveanu
Co-authored papers 7
Friedhelm Hildebrandt
Boston Children's Hospital
Co-authored papers 7
Matthias Kretzler
University of Michigan ann arbor
Co-authored papers 6
Release 1.2