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Author Details

Brendan J Keating
Perelman School of Medicine, University of Pennsylvania
2003
157
50
PMIDPaper TitleJournal TitlePublished Year
36732776LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genes.BioData Min2023
37598688Immune response after pig-to-human kidney xenotransplantation: a multimodal phenotyping study.Lancet2023
37488288Pig-to-human heart xenotransplantation in two recently deceased human recipients.Nat Med2023
37507685Gut microbiota analyses of inflammatory bowel diseases from a representative Saudi population.BMC Gastroenterol2023
37158713Family-base rare variant association analysis in Saudi Arabian hydrocephalus subjects using whole exome sequencing.J Neurosurg Sci2023
37151104Unsupervised mRNA-seq classification of heart transplant endomyocardial biopsies.Clin Transplant2023
36973604Whole-exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk.Funct Integr Genomics2023
36846987Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.J Am Heart Assoc2023
36846569Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls.Front Mol Neurosci2023
34974452The Impact of Donor and Recipient Genetic Variation on Outcomes After Solid Organ Transplantation: A Scoping Review and Future Perspectives.Transplantation2022
35393535Donor and recipient polygenic risk scores influence the risk of post-transplant diabetes.Nat Med2022
36539902Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci.Hum Genomics2022
35968930Testing the application of polygenic risk scores in the transplant setting - Relevance for precision medicine.Clin Transl Med2022
36204191Impact of <i>CYP3A5</i> Status on the Clinical and Financial Outcomes Among African American Kidney Transplant Recipients.Transplant Direct2022
35317953Whole transcriptome profiling of prospective endomyocardial biopsies reveals prognostic and diagnostic signatures of cardiac allograft rejection.J Heart Lung Transplant2022
33401139Noninvasive biomarkers for prediction and diagnosis of heart transplantation rejection.Transplant Rev (Orlando)2021
33713608Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.Am J Hum Genet2021
33677556Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.Eur Heart J2021
33735480Early detection of SARS-CoV-2 and other infections in solid organ transplant recipients and household members using wearable devices.Transpl Int2021
34805493Design and Methods of the Validating Injury to the Renal Transplant Using Urinary Signatures (VIRTUUS) Study in Children.Transplant Direct2021
34041755Exome sequencing in high and low fetal haemoglobin Arab-Indian haplotype sickle cell disease.Br J Haematol2021
32454123Genome-wide non-HLA donor-recipient genetic differences influence renal allograft survival via early allograft fibrosis.Kidney Int2020
31937769Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.Nat Commun2020
33134492Rejection-associated Mitochondrial Impairment After Heart Transplantation.Transplant Direct2020
32662547Pharmacogenomics in kidney transplant recipients and potential for integration into practice.J Clin Pharm Ther2020
32783273Joint testing of donor and recipient genetic matching scores and recipient genotype has robust power for finding genes associated with transplant outcomes.Genet Epidemiol2020
32506790Genomics and Liver Transplantation: Genomic Biomarkers for the Diagnosis of Acute Cellular Rejection.Liver Transpl2020
32400091Polygenic risk score of non-melanoma skin cancer predicts post-transplant skin cancer across multiple organ types.Clin Transplant2020
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
31787968Current and Future Approaches for Monitoring Responses to Anti-complement Therapeutics.Front Immunol2019
31803228Genome-Wide Study Updates in the International Genetics and Translational Research in Transplantation Network (iGeneTRAiN).Front Genet2019
30085400Polygenic risk score as a determinant of risk of non-melanoma skin cancer in a European-descent renal transplant cohort.Am J Transplant2019
31488014Exome sequencing of Saudi Arabian patients with ADPKD.Ren Fail2019
30953600Tacrolimus troughs and genetic determinants of metabolism in kidney transplant recipients: A comparison of four ancestry groups.Am J Transplant2019
30773281Contribution of non-HLA incompatibility between donor and recipient to kidney allograft survival: genome-wide analysis in a prospective cohort.Lancet2019
30920136The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.Am J Transplant2019
30801552Genetic Variants Associated With Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome-wide Association Studies.Transplantation2019
30882026Non-HLA Genetic Factors and Their Influence on Heart Transplant Outcomes: A Systematic Review.Transplant Direct2019
30456907Development and evaluation of a transfusion medicine genome wide genotyping array.Transfusion2019
29321517Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study.J Hum Genet2018
29967039Gene-Centric Analysis of Preeclampsia Identifies Maternal Association at <i>PLEKHG1</i>.Hypertension2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
28115737Cannabis use and risk of schizophrenia: a Mendelian randomization study.Mol Psychiatry2018
29363220Applying genomics in heart transplantation.Transpl Int2018
29665793Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations.BMC Nephrol2018
29654215<i>NPHP1</i> (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD.J Am Soc Nephrol2018
29735024Immunologic Monitoring to Personalize Immunosuppression After Liver Transplant.Gastroenterol Clin North Am2018
27344648Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder.JIMD Rep2017
28196478Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing.BMC Med Genet2017
29106476Correcting the Standard Errors of 2-Stage Residual Inclusion Estimators for Mendelian Randomization Studies.Am J Epidemiol2017
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Joel N Hirschhorn
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Cameron D Palmer
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Yvonne T van der Schouw
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Cecilia E Kim
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Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
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Struan F A Grant
Center for Spatial and Functional Genomics, The Children's Hospital of Philadelphia
Co-authored papers 11
Juan P Casas
Co-authored papers 11
Michele K Evans
National Institute on Aging
Co-authored papers 10
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 10
Release 1.2