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Author Details

Hemang Parikh
Health Informatics Institute, University of South Florida
2004
51
25
PMIDPaper TitleJournal TitlePublished Year
36314086Data Mining Framework for Discovering and Clustering Phenotypes of Atypical Diabetes.J Clin Endocrinol Metab2023
36314086Data Mining Framework for Discovering and Clustering Phenotypes of Atypical Diabetes.J Clin Endocrinol Metab2023
36867433Interaction Between Dietary Iron Intake and Genetically Determined Iron Overload: Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in the TEDDY Study.Diabetes Care2023
37115548Epigenetic Age in Peripheral Blood Among Children, Adolescent, and Adult Survivors of Childhood Cancer.JAMA Netw Open2023
37496087ISLET: individual-specific reference panel recovery improves cell-type-specific inference.Genome Biol2023
37496087ISLET: individual-specific reference panel recovery improves cell-type-specific inference.Genome Biol2023
37115548Epigenetic Age in Peripheral Blood Among Children, Adolescent, and Adult Survivors of Childhood Cancer.JAMA Netw Open2023
36867433Interaction Between Dietary Iron Intake and Genetically Determined Iron Overload: Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in the TEDDY Study.Diabetes Care2023
35780170High-throughput muscle fiber typing from RNA sequencing data.Skelet Muscle2022
35780170High-throughput muscle fiber typing from RNA sequencing data.Skelet Muscle2022
33404683First-appearing islet autoantibodies for type 1 diabetes in young children: maternal life events during pregnancy and the child's genetic risk.Diabetologia2021
33639916Relationship between insulin sensitivity and gene expression in human skeletal muscle.BMC Endocr Disord2021
33790023Transcriptional networks in at-risk individuals identify signatures of type 1 diabetes progression.Sci Transl Med2021
33404683First-appearing islet autoantibodies for type 1 diabetes in young children: maternal life events during pregnancy and the child's genetic risk.Diabetologia2021
33790023Transcriptional networks in at-risk individuals identify signatures of type 1 diabetes progression.Sci Transl Med2021
33639916Relationship between insulin sensitivity and gene expression in human skeletal muscle.BMC Endocr Disord2021
31728565Plasma ascorbic acid and the risk of islet autoimmunity and type 1 diabetes: the TEDDY study.Diabetologia2020
32029481Longitudinal Metabolome-Wide Signals Prior to the Appearance of a First Islet Autoantibody in Children Participating in the TEDDY Study.Diabetes2020
31728565Plasma ascorbic acid and the risk of islet autoimmunity and type 1 diabetes: the TEDDY study.Diabetologia2020
32029481Longitudinal Metabolome-Wide Signals Prior to the Appearance of a First Islet Autoantibody in Children Participating in the TEDDY Study.Diabetes2020
30936564An open resource for accurately benchmarking small variant and reference calls.Nat Biotechnol2019
30936564An open resource for accurately benchmarking small variant and reference calls.Nat Biotechnol2019
28634199Characterising <i>cis</i>-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues.Gut2018
28634199Characterising <i>cis</i>-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues.Gut2018
30352204Serum biomarkers of glucocorticoid response and safety in anti-neutrophil cytoplasmic antibody-associated vasculitis and juvenile dermatomyositis.Steroids2018
29724730Metabolic pathways and immunometabolism in rare kidney diseases.Ann Rheum Dis2018
30352204Serum biomarkers of glucocorticoid response and safety in anti-neutrophil cytoplasmic antibody-associated vasculitis and juvenile dermatomyositis.Steroids2018
29724730Metabolic pathways and immunometabolism in rare kidney diseases.Ann Rheum Dis2018
28759004A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.Nat Genet2017
28759004A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.Nat Genet2017
26772178svclassify: a method to establish benchmark structural variant calls.BMC Genomics2016
26772178svclassify: a method to establish benchmark structural variant calls.BMC Genomics2016
28172817Functional characterization of a chr13q22.1 pancreatic cancer risk locus reveals long-range interaction and allele-specific effects on DIS3 expression.Hum Mol Genet2016
28172817Functional characterization of a chr13q22.1 pancreatic cancer risk locus reveals long-range interaction and allele-specific effects on DIS3 expression.Hum Mol Genet2016
25035170Identification and validation of TGFBI as a promising prognosis marker of clear cell renal cell carcinoma.Urol Oncol2015
26338460Less pronounced response to exercise in healthy relatives to type 2 diabetic subjects compared with controls.J Appl Physiol (1985)2015
25035170Identification and validation of TGFBI as a promising prognosis marker of clear cell renal cell carcinoma.Urol Oncol2015
26338460Less pronounced response to exercise in healthy relatives to type 2 diabetic subjects compared with controls.J Appl Physiol (1985)2015
24648346CLPTM1L promotes growth and enhances aneuploidy in pancreatic cancer cells.Cancer Res2014
25233928Transcriptome analysis of pancreatic cancer reveals a tumor suppressor function for HNF1A.Carcinogenesis2014
25027329Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.Hum Mol Genet2014
25135760Smoking induces overexpression of immediate early genes in active Graves' ophthalmopathy.Thyroid2014
24648346CLPTM1L promotes growth and enhances aneuploidy in pancreatic cancer cells.Cancer Res2014
25233928Transcriptome analysis of pancreatic cancer reveals a tumor suppressor function for HNF1A.Carcinogenesis2014
25027329Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.Hum Mol Genet2014
25135760Smoking induces overexpression of immediate early genes in active Graves' ophthalmopathy.Thyroid2014
23295781A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk.Pancreas2013
24053169An integrated transcriptome and epigenome analysis identifies a novel candidate gene for pancreatic cancer.BMC Med Genomics2013
23295781A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk.Pancreas2013
23573233Characterization of SNPs associated with prostate cancer in men of Ashkenazic descent from the set of GWAS identified SNPs: impact of cancer family history and cumulative SNP risk prediction.PLoS One2013
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Harvard T.H. Chan School of Public Health
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Human Phenome Institute and Shanghai Cancer Center, Fudan University
Co-authored papers 3
National Cancer Institute, National Institutes of Health, Inc.
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VA Boston Healthcare System
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Spanish National Cancer Research Centre
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