Beena S. Suresh

Ooty, TN, India

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Microbiologically influenced corrosion dynamics and technological innovations in monitoring and control.

Microbiologically influenced corrosion dynamics and technological innovations in monitoring and control.

Journal: Journal of microbiological methods

Published: January 06, 2026

Meta-LLSTM: meta-learning enhanced learnable LSTM for retail sales forecasting.

Meta-LLSTM: meta-learning enhanced learnable LSTM for retail sales forecasting.

Journal: Scientific reports

Published: November 17, 2025

Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.

Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.

Journal: Orphanet journal of rare diseases

Published: April 18, 2024

A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage.

A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage.

Journal: Molecular genetics & genomic medicine

Published: August 13, 2023

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.

Journal: Brain : a journal of neurology

Published: April 26, 2023

Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.

Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.

Journal: Clinical genetics

Published: January 25, 2021

Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.

Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.

Journal: Frontiers in immunology

Published: September 30, 2020

Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family.

Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family.

Journal: Journal of clinical pathology

Published: August 24, 2020

Bain type of X-linked syndromic mental retardation in a male with a pathogenic variant in HNRNPH2.

Bain type of X-linked syndromic mental retardation in a male with a pathogenic variant in HNRNPH2.

Journal: American journal of medical genetics. Part A

Published: February 19, 2019

Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta.

Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta.

Journal: American journal of medical genetics. Part A

Published: October 19, 2018

A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV).

A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV).

Journal: Neuro-ophthalmology (Aeolus Press)

Published: April 16, 2018

In vitro studies on medicinal plants used against bacterial diabetic foot ulcer (BDFU) and urinary tract infected (UTI) causing pathogens.

In vitro studies on medicinal plants used against bacterial diabetic foot ulcer (BDFU) and urinary tract infected (UTI) causing pathogens.

Journal: Journal of parasitic diseases : official organ of the Indian Society for Parasitology

Published: July 08, 2014

Showing 1-12 of 15

Last Updated: 09/26/2026