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Author Details
Full Name
Hemang Parikh
Affiliation
Health Informatics Institute, University of South Florida
ORCID
Career Start Year
2004
Papers
51
H Index
25
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36314086
Data Mining Framework for Discovering and Clustering Phenotypes of Atypical Diabetes.
J Clin Endocrinol Metab
2023
36314086
Data Mining Framework for Discovering and Clustering Phenotypes of Atypical Diabetes.
J Clin Endocrinol Metab
2023
36867433
Interaction Between Dietary Iron Intake and Genetically Determined Iron Overload: Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in the TEDDY Study.
Diabetes Care
2023
37115548
Epigenetic Age in Peripheral Blood Among Children, Adolescent, and Adult Survivors of Childhood Cancer.
JAMA Netw Open
2023
37496087
ISLET: individual-specific reference panel recovery improves cell-type-specific inference.
Genome Biol
2023
37496087
ISLET: individual-specific reference panel recovery improves cell-type-specific inference.
Genome Biol
2023
37115548
Epigenetic Age in Peripheral Blood Among Children, Adolescent, and Adult Survivors of Childhood Cancer.
JAMA Netw Open
2023
36867433
Interaction Between Dietary Iron Intake and Genetically Determined Iron Overload: Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in the TEDDY Study.
Diabetes Care
2023
35780170
High-throughput muscle fiber typing from RNA sequencing data.
Skelet Muscle
2022
35780170
High-throughput muscle fiber typing from RNA sequencing data.
Skelet Muscle
2022
33404683
First-appearing islet autoantibodies for type 1 diabetes in young children: maternal life events during pregnancy and the child's genetic risk.
Diabetologia
2021
33639916
Relationship between insulin sensitivity and gene expression in human skeletal muscle.
BMC Endocr Disord
2021
33790023
Transcriptional networks in at-risk individuals identify signatures of type 1 diabetes progression.
Sci Transl Med
2021
33404683
First-appearing islet autoantibodies for type 1 diabetes in young children: maternal life events during pregnancy and the child's genetic risk.
Diabetologia
2021
33790023
Transcriptional networks in at-risk individuals identify signatures of type 1 diabetes progression.
Sci Transl Med
2021
33639916
Relationship between insulin sensitivity and gene expression in human skeletal muscle.
BMC Endocr Disord
2021
31728565
Plasma ascorbic acid and the risk of islet autoimmunity and type 1 diabetes: the TEDDY study.
Diabetologia
2020
32029481
Longitudinal Metabolome-Wide Signals Prior to the Appearance of a First Islet Autoantibody in Children Participating in the TEDDY Study.
Diabetes
2020
31728565
Plasma ascorbic acid and the risk of islet autoimmunity and type 1 diabetes: the TEDDY study.
Diabetologia
2020
32029481
Longitudinal Metabolome-Wide Signals Prior to the Appearance of a First Islet Autoantibody in Children Participating in the TEDDY Study.
Diabetes
2020
30936564
An open resource for accurately benchmarking small variant and reference calls.
Nat Biotechnol
2019
30936564
An open resource for accurately benchmarking small variant and reference calls.
Nat Biotechnol
2019
28634199
Characterising <i>cis</i>-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues.
Gut
2018
28634199
Characterising <i>cis</i>-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues.
Gut
2018
30352204
Serum biomarkers of glucocorticoid response and safety in anti-neutrophil cytoplasmic antibody-associated vasculitis and juvenile dermatomyositis.
Steroids
2018
29724730
Metabolic pathways and immunometabolism in rare kidney diseases.
Ann Rheum Dis
2018
30352204
Serum biomarkers of glucocorticoid response and safety in anti-neutrophil cytoplasmic antibody-associated vasculitis and juvenile dermatomyositis.
Steroids
2018
29724730
Metabolic pathways and immunometabolism in rare kidney diseases.
Ann Rheum Dis
2018
28759004
A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.
Nat Genet
2017
28759004
A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.
Nat Genet
2017
26772178
svclassify: a method to establish benchmark structural variant calls.
BMC Genomics
2016
26772178
svclassify: a method to establish benchmark structural variant calls.
BMC Genomics
2016
28172817
Functional characterization of a chr13q22.1 pancreatic cancer risk locus reveals long-range interaction and allele-specific effects on DIS3 expression.
Hum Mol Genet
2016
28172817
Functional characterization of a chr13q22.1 pancreatic cancer risk locus reveals long-range interaction and allele-specific effects on DIS3 expression.
Hum Mol Genet
2016
25035170
Identification and validation of TGFBI as a promising prognosis marker of clear cell renal cell carcinoma.
Urol Oncol
2015
26338460
Less pronounced response to exercise in healthy relatives to type 2 diabetic subjects compared with controls.
J Appl Physiol (1985)
2015
25035170
Identification and validation of TGFBI as a promising prognosis marker of clear cell renal cell carcinoma.
Urol Oncol
2015
26338460
Less pronounced response to exercise in healthy relatives to type 2 diabetic subjects compared with controls.
J Appl Physiol (1985)
2015
24648346
CLPTM1L promotes growth and enhances aneuploidy in pancreatic cancer cells.
Cancer Res
2014
25233928
Transcriptome analysis of pancreatic cancer reveals a tumor suppressor function for HNF1A.
Carcinogenesis
2014
25027329
Imputation 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 Genet
2014
25135760
Smoking induces overexpression of immediate early genes in active Graves' ophthalmopathy.
Thyroid
2014
24648346
CLPTM1L promotes growth and enhances aneuploidy in pancreatic cancer cells.
Cancer Res
2014
25233928
Transcriptome analysis of pancreatic cancer reveals a tumor suppressor function for HNF1A.
Carcinogenesis
2014
25027329
Imputation 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 Genet
2014
25135760
Smoking induces overexpression of immediate early genes in active Graves' ophthalmopathy.
Thyroid
2014
23295781
A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk.
Pancreas
2013
24053169
An integrated transcriptome and epigenome analysis identifies a novel candidate gene for pancreatic cancer.
BMC Med Genomics
2013
23295781
A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk.
Pancreas
2013
23573233
Characterization 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 One
2013
1 - 50 of 102
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