Author

Ramesh Reddy

Observed name: Reddy, Ramesh

Institutions: First Affiliated Hospital Zhejiang University, Zhejiang University

Observed institutions: University of Vermont, Jawaharlal Nehru Centre for Advanced Scientific Research, McGill University Health Centre, First Affiliated Hospital Zhejiang University, Research Institute of the McGill University Health Centre, McGill University, Zhejiang University

OpenAlex ID: A5055987052

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles

2018 · Ngoc Minh Phuong Nguyen, Zhao-Jia Ge, et al. · The American Journal of Human Genetics · 115

Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7

2012 · Ramesh Reddy, Elie Akoury, et al. · European Journal of Human Genetics · 77

An idiopathic epilepsy syndrome linked to 3q13.3‐q21 and missense mutations in the extracellular calcium sensing receptor gene

2008 · Ashish Kapoor, Parthasarathy Satishchandra, et al. · Annals of Neurology · 76

Comprehensive genotype–phenotype correlations between NLRP7 mutations and the balance between embryonic tissue differentiation and trophoblastic proliferation

2014 · Ngoc Minh Phuong Nguyen, Li Zhang, et al. · Journal of Medical Genetics · 40

A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3

2009 · Rinki Ratnapriya, Parthasarthy Satishchandra, et al. · Human Genetics · 40

The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

2016 · Ramesh Reddy, Ngoc M P Nguyen, et al. · European Journal of Human Genetics · 34

Recurrent Pregnancy Loss in a Woman With NLRP7 Mutation

2013 · Lucia Brown, Sharon Mount, et al. · International Journal of Gynecological Pathology · 21

Molecular Genetics of the Usher Syndrome in Lebanon: Identification of 11 Novel Protein Truncating Mutations by Whole Exome Sequencing

2014 · Ramesh Reddy, Somayyeh Fahiminiya, et al. · PLoS ONE · 11

Erratum: The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

2016 · Ramesh Reddy, Ngoc M P Nguyen, et al. · European Journal of Human Genetics · 5

Associations with Single Rare Heterozygous NLRP7 Variants for Chinese Patients with Sporadic Gestational Trophoblastic Diseases

2020 · Peiwen Zhang, Xinying Yu, et al. · Research Square

Erratum: The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions

2020 · Nunez, Kristin P, Reddy, Ramesh, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)

Works count: 11

Citation count: 419

H-index: 8

I10-index: 8