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Samarth Bhatt

Malaviya National Institute of Technology Jaipur(IN)

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78

Papers

2.6K

Citations

20

h-index

29

i10-index

Samarth Bhatt is an academic researcher from Malaviya National Institute of Technology Jaipur. The author has contributed to research in topics: Genomic variations and chromosomal abnormalities & Chromosomal and Genetic Variations & Prenatal Screening and Diagnostics. The author has an h-index of 20, co-authored 67 publications.

ORCID: 0000-0001-5706-4572

Research Topics

Genomic variations and chromosomal abnormalities Chromosomal and Genetic Variations Prenatal Screening and Diagnostics Genetics and Neurodevelopmental Disorders Genomics and Chromatin Dynamics

Papers by this author

works

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

2009 · The American Journal of Human Genetics · 513 citations

https://doi.org/10.1016/j.ajhg.2009.05.005

Paweł Stankiewicz Partha Sen Samarth Bhatt Mekayla A. Storer

BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma

2017 · Clinical Epigenetics · 129 citations

https://doi.org/10.1186/s13148-017-0367-x

Darlene A. Kertes Samarth Bhatt Hayley S. Kamin David A. Hughes

Chromosome distribution in human sperm – a 3D multicolor banding-study

2008 · Molecular Cytogenetics · 87 citations

https://doi.org/10.1186/1755-8166-1-25

Marina Manvelyan Friederike Hunstig Samarth Bhatt Kristin Mrasek

Heteromorphic variants of chromosome 9

2013 · Molecular Cytogenetics · 47 citations

https://doi.org/10.1186/1755-8166-6-14

Nadezda Kosyakova Ani Grigorian Thomas Liehr Marina Manvelyan

Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon

2008 · Molecular Cytogenetics · 32 citations

https://doi.org/10.1186/1755-8166-1-9

Marina Manvelyan Friederike Hunstig Kristin Mrasek Samarth Bhatt

Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability

2016 · Orphanet Journal of Rare Diseases · 28 citations

https://doi.org/10.1186/s13023-016-0439-6

Valerie V. Maduro Barbara N. Pusey Praveen F. Cherukuri Paul Atkins

Research topics

topics

Genomic variations and chromosomal abnormalities

Chromosomal and Genetic Variations

Prenatal Screening and Diagnostics

Genetics and Neurodevelopmental Disorders

Genomics and Chromatin Dynamics

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