Jayesh Sheth - Concepedia

Author

Jayesh Sheth

Institute of Human Genetics ORCID

Also Known As

Anita Nadkarni, J J Sheth, J Sheth, J. J. Sheth, J. Sheth, Jayesh J Sheth, Jayesh J. Sheth, Jayesh Sheth, Sheth, Jayesh

159

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Institute of Human Genetics Amrita Institute of Medical Sciences and Research Centre Centre For Human Genetics KLE Society Hospital Institute of Genetics and Hospital for Genetic Diseases

About

Jayesh Sheth is an author at Institute of Human Genetics specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	15	397
2	Public Health	5	5	156
3	Education	1	1	15
4	Engineering	1	1	11
5	Natural Sciences	1	1	12

Jayesh Sheth

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Ring chromosome 9 in a dysmorphic child Jayesh Sheth, Rajesh Joshi, Frenny Sheth The Indian Journal of Pediatrics	2007	73
Does vitamin D play a significant role in type 2 diabetes? Jayesh Sheth, Ankna Shah, Frenny Sheth, BMC Endocrine Disorders	2015	69
Burden of Lysosomal Storage Disorders in India: Experience of 387 Affected Children from a Single Diagnostic Facility Jayesh Sheth, Mehul Mistri, Frenny Sheth, JIMD Reports	2013	60
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation Jayesh Sheth, Riddhi Bhavsar, Mehul Mistri, BMC Medical Genetics	2019	60
Maternal one‐carbon metabolism, <i>MTHFR</i> and <i>TCN2</i> genotypes and neural tube defects in India Koumudi Godbole, Panjalingam Gayathri, Smita Ghule, Birth Defects Research Part A Clinical and Molecular Teratology	2011	59
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility G Vinci, Raja Brauner, Attila Tar, Fertility and Sterility InfertilityDevelopmental BiologyTspyl1 GeneCytogeneticsGenetic Disorder	2009	57
The association of dyslipidemia and obesity with glycated hemoglobin Jayesh Sheth, Ankna Shah, Frenny Sheth, Clinical Diabetes and Endocrinology	2015	55
Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India Mehul Mistri, Parag Tamhankar, Frenny Sheth, PLoS ONE Hexa GeneNeurological DisorderGeneticsPathologyMolecular Genetics	2012	44
The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region Uppala Radhakrishna, Jean‐Louis Blouin, Hamid Mehenni, American Journal of Medical Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsClouston Syndrome	1997	43
Genomewide Scan for Nonsyndromic Cleft Lip and Palate in Multigenerational Indian Families Reveals Significant Evidence of Linkage at 13q33.1-34 Uppala Radhakrishna, Uppala Ratnamala, Mathew Gaines, The American Journal of Human Genetics Developmental BiologyNonsyndromic Cleft LipGenetic DisorderGeneticsGenetic Epidemiology	2006	37

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