Publications:

---

Acute liver failure associated with lamotrigine in children with epilepsy: A report of two cases and thoughts on pharmacogenomics.

Epilepsy & Behavior Reports

Deng, Jie J; Fu, Zheng-Ran ZR; Wang, Long L; Liu, Jun J; Chen, Chun-Hong CH; Fang, Fang F; Wang, Xiao-Ling XL

Publication Date: 2022

Variant appearance in text: rs10188577

PubMed Link: 36345310

Variant Present in the following documents:

• main.pdf

View BVdb publication page

---

Polymorphisms of the sodium voltage-gated channel, alpha subunit 1 (SCN1A -A3184G) gene among children with non-lesional epilepsy: a case-control study.

Italian Journal Of Pediatrics

Ghazala, Esraa E; Shahin, Doaa A DA; Wahba, Yahya Y

Publication Date: 2022-09-02

Variant appearance in text: rs10188577

PubMed Link: 36056404

Variant Present in the following documents:

• Main text
• 13052_2022_Article_1350.pdf

View BVdb publication page

---

Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population.

Annals Of Medicine

Alghamdi, Mansour A MA; Al-Eitan, Laith N LN; Asiri, Ashwag A; Rababa'h, Doaa M DM; Alqahtani, Sultan A SA; Aldarami, Mohammed S MS; Alsaeedi, Manar A MA; Almuidh, Raghad S RS; Alzahrani, Abdulbari A AA; Sakah, Ahmad H AH; El Nashar, Eman Mohamad EM; Otaif, Mansour Y MY; Abdel Ghaffar, Nawal F NF

Publication Date: 2022-12

Variant appearance in text: rs10188577

PubMed Link: 35801810

Variant Present in the following documents:

• Main text
• IANN_54_2096257.pdf

View BVdb publication page

---

Association Between SCN1A rs2298771, SCN1A rs10188577, SCN2A rs17183814, and SCN2A rs2304016 Polymorphisms and Responsiveness to Antiepileptic Drugs: A Meta-Analysis.

Frontiers In Neurology

Li, Mengmeng M; Zhong, Rui R; Lu, Yingxue Y; Zhao, Qian Q; Li, Guangjian G; Lin, Weihong W

Publication Date: 2020

Variant appearance in text: rs10188577

PubMed Link: 33519675

Variant Present in the following documents:

• Main text
• fneur-11-591828.pdf

View BVdb publication page

---

Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs10188577

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

---

Association of SCN1A gene polymorphism with antiepileptic drug responsiveness in the population of Thrace, Greece.

Archives Of Medical Science : Ams

Angelopoulou, Christina C; Veletza, Stavroula S; Heliopoulos, Ioannis I; Vadikolias, Konstantinos K; Tripsianis, Grigorios G; Stathi, Chrysa C; Piperidou, Charitomeni C

Publication Date: 2017-02-01

Variant appearance in text: rs10188577

PubMed Link: 28144265

Variant Present in the following documents:

• Main text
• AMS-13-27502.pdf

View BVdb publication page

---

Evaluating the Role of Genetic Variants on first-line antiepileptic drug response in North India: Significance of SCN1A and GABRA1 Gene Variants in Phenytoin Monotherapy and its Serum Drug Levels.

Cns Neuroscience & Therapeutics

Baghel, Ruchi R; Grover, Sandeep S; Kaur, Harpreet H; Jajodia, Ajay A; Rawat, Chitra C; Srivastava, Ankit A; Kushwaha, Suman S; Agarwal, Rachna R; Sharma, Sangeeta S; Kukreti, Ritushree R

Publication Date: 2016-09

Variant appearance in text: rs10188577

PubMed Link: 27245092

Variant Present in the following documents:

• Main text

View BVdb publication page

---