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Dr ARSHIA ANGURAL

vidwan id: 432832
Female

Assistant Professor, Department of Medical Genetics
JSS Academy of Higher Education & Research

Expertise

  • Biology

Publications

Total Articles 17
Books 0
Proceedings 0

Publications

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Scopus

Citations 79
h-index 5

CrossRef

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Citations 69
h-index 5
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Professional Recognition

2019

International Travel Scheme (ITS) (travel grant)

DST-SERB

Community & Membership

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Bio

A biotechnologist with a Clinical Genetics research background, having an ultimate objective of contributing towards the betterment of human society, my research work is focused on delineation and understanding the underpinning molecular factors and their pathophysiology responsible for precipitating human genetic diseases, especially rare diseases, using state-of-the art techniques including Sequencing technologies (Sanger Sequencing and NGS) and LC-MS/MS.

Personal Details

  • Female
  • Assistant Professor , JSS Academy of Higher Education & Research
  • JSS Medical College and Hospital
Ph.D.
Other Institute 2020
Assistant Professor Jun 2022 – Present
JSS Academy of Higher Education & Research | Department of Medical Genetics

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Co-Authors (13)

Akila

Prof Akila Prashant

JSS Medical College, Mysore

Ankit

Dr Ankit Mahajan

Jammu University

Himanshu

Dr Himanshu Gupta

GLA University, Mathura

Indu

Dr Indu Sharma

Assam University

K

Prof K Satyamoorthy

Shri Dharmasthala Manjunatheshwara University

Manoj Kumar

Dr Manoj Kumar Dhar

Jammu University

Parvinder

Dr Parvinder Kumar

Jammu University

Saadi Abdul

Dr Saadi Abdul Vahab

Manipal Academy of Higher Education, Manipal

Siddharth

Mr Siddharth Birla

JSS Academy of Higher Education & Research

Swarkar

Prof Swarkar Sharma

Central University of Jammu

Kumarasamy

Dr Kumarasamy Thangaraj

CSIR-Centre for Cellular and Molecular Biology

Vinod

Dr Vinod Singh

Shri Mata Vaishno Devi University

Scholarly Work

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Scholarly Publications

Birth Defects: A Call for Action.

Open Access
other
Authors: Angural, A., Birla, S., Srinivas, A., Prasanth, A. and Hattur, B.G.

Cost-effective Whole Exome Sequencing discovers pathogenic variant causing Neurofibromatosis type 1 in a family from Jammu and Kashmir, India.

Open Access
Article
Authors: Spolia, A., Angural, A., Sharma, V., Shipra, Razdan, S., Dhar, M.K., Mahajan, A., Verma, V., Pandita, K.K., Sharma, S., Rai, E.

Redefining the polypill: pros and cons in cardiovascular precision medicine

Open Access
Review
Authors: Siddharth Birla ., Arshia Angural ., Arya Madathumchalil ., Ritika V. Shende ., Sharvani V. Shastry ., Manjappa Mahadevappa ., Sunil Kumar Shambhu ., Prashant Vishwanath ., Akila Prashant .,

Genetic Characterisation of Pantothenate Kinase Associated Neurodegeneration (PKAN) in a Consanguineous Family from Jammu and Kashmir, India

Open Access
Article
Authors: Spolia, A., Shipra, Angural, A., Singh, H., Verma, V., Pandita, K.K., Sharma, S., Rai, E.

Missense Variation in TPP1 Gene causes Neuronal Ceroid Lipofuscinosis Type 2 in a Family from Jammu and Kashmir-India

Open Access
other
Authors: Angural, A., Ponnusamy, K., Langeh, D., Kumari, M., Spolia, A., Rai, E., Sharma, A., Pandita, K.K., Sharma, S.

Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir – India

Open Access
Review
Authors: Angural A.;Spolia A.;Mahajan A.;Verma V.;Sharma A.;Kumar P.;Dhar M.K.;Pandita K.K.;Rai E.;Sharma S.

A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications.

Open Access
Article
Authors: Angural, A., Sharma, I., Pandoh, P., Sharma, V., Spolia, A., Rai, E., Singh, V., Razdan, S., Pandita, K.K., Sharma, S.

Replication of MACF1 gene variant rs2296172 with type 2 diabetes susceptibility in the Bania population group of Punjab, India

Open Access
article
Authors: Sharma, V., Sethi, I., Sharma, I., Singh, G., Mahajan, A., Angural, A., Bhanwer, A.J.S., Dhar, M. K., Pandita, K. K., Singh, V., Rai, E., Sharma, S.