Synergistic association of STX 1A and VAMP 2 with cryptogenic epilepsy in North Indian population-Reference-Cited by-同舟云学术

Synergistic association of STX 1A and VAMP 2 with cryptogenic epilepsy in North Indian population

Published:2016-06-14 Issue:7 Volume:6 Page:
ISSN:2162-3279
Container-title:Brain and Behavior
language:en
Short-container-title:Brain Behav

Author:

Baghel Ruchi¹,Grover Sandeep¹²,Kaur Harpreet¹,Jajodia Ajay¹,Parween Shama¹,Sinha Juhi¹,Srivastava Ankit¹,Srivastava Achal Kumar³,Bala Kiran⁴,Chandna Puneet⁵,Kushwaha Suman⁴,Agarwal Rachna⁴,Kukreti Ritushree¹

Affiliation:

1. Council of Scientific and Industrial Research (CSIR) Institute of Genomics and Integrative Biology (IGIB) Mall Road Delhi 110 007 India

2. Division of Pneumonology‐Immunology Department of Paediatrics Charité University Medical Centre Berlin Germany

3. Neurology Department Neuroscience Centre All India Institute of Medical Sciences (AIIMS) New Delhi India

4. Institute of Human Behavior & Allied Sciences (IHBAS) Dilshad Garden Delhi 110 095 India

5. AceProbe Technologies (India) Pvt. Ltd. New Delhi India

Funder

Indian Council of Medical Research

Council for Scientific and Industrial Research

Publisher

Wiley

Subject

Behavioral Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/brb3.490

Reference32 articles.

1. Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder

2. Research Highlights: Highlights from the latest articles focusing on a new gene set for better drug response prediction of epilepsy patients

3. Epilepsy as a Neurodevelopmental Disorder

4. Regulators of synaptic transmission: Roles in the pathogenesis and treatment of epilepsy

5. Proposal for revised clinical and electroencephalographic classification of epileptic seizures. From the Commission on Classification and Terminology of the International League Against Epilepsy;Epilepsy, C.o.C.a.T.o.t.I.L.A;Epilepsia,1981

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1. Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder;European Journal of Human Genetics;2023-04-07

2. Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy;European Journal of Human Genetics;2022-12-23

3. Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy;2022-04-21

4. Distinct Epileptogenic Mechanisms Associated with Seizures in Wolf-Hirschhorn Syndrome;Molecular Neurobiology;2022-03-12

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