PubMed (OMIM) for id: 3785

Year	Number of Results
1968	1
1978	1
1979	1
1980	2
1982	1
1984	1
1988	1
1989	1
1991	1
1992	2
1993	1
1994	2
1998	5
1999	1
2000	2
2001	1
2003	3
2004	1
2005	1
2006	1
2007	2
2009	2
2012	2
2013	1
2024	0

1

Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.

Kato M, Yamagata T, Kubota M, Arai H, Yamashita S, Nakagawa T, Fujii T, Sugai K, Imai K, Uster T, Chitayat D, Weiss S, Kashii H, Kusano R, Matsumoto A, Nakamura K, Oyazato Y, Maeno M, Nishiyama K, Kodera H, Nakashima M, Tsurusaki Y, Miyake N, Saito K, Hayasaka K, Matsumoto N, Saitsu H. Kato M, et al. Epilepsia. 2013 Jul;54(7):1282-7. doi: 10.1111/epi.12200. Epub 2013 Apr 26. Epilepsia. 2013. PMID: 23621294 Free article.

2

Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.

Saitsu H, Kato M, Koide A, Goto T, Fujita T, Nishiyama K, Tsurusaki Y, Doi H, Miyake N, Hayasaka K, Matsumoto N. Saitsu H, et al. Ann Neurol. 2012 Aug;72(2):298-300. doi: 10.1002/ana.23620. Ann Neurol. 2012. PMID: 22926866 No abstract available.

3

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P. Weckhuysen S, et al. Ann Neurol. 2012 Jan;71(1):15-25. doi: 10.1002/ana.22644. Ann Neurol. 2012. PMID: 22275249

4

Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures.

Kurahashi H, Wang JW, Ishii A, Kojima T, Wakai S, Kizawa T, Fujimoto Y, Kikkawa K, Yoshimura K, Inoue T, Yasumoto S, Ogawa A, Kaneko S, Hirose S. Kurahashi H, et al. Neurology. 2009 Oct 13;73(15):1214-7. doi: 10.1212/WNL.0b013e3181bc0158. Neurology. 2009. PMID: 19822871

5

Genetics of epilepsy syndromes starting in the first year of life.

Deprez L, Jansen A, De Jonghe P. Deprez L, et al. Neurology. 2009 Jan 20;72(3):273-81. doi: 10.1212/01.wnl.0000339494.76377.d6. Neurology. 2009. PMID: 19153375 Review.

6

Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations.

Wuttke TV, Jurkat-Rott K, Paulus W, Garncarek M, Lehmann-Horn F, Lerche H. Wuttke TV, et al. Neurology. 2007 Nov 27;69(22):2045-53. doi: 10.1212/01.wnl.0000275523.95103.36. Epub 2007 Sep 13. Neurology. 2007. PMID: 17872363

7

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.

Heron SE, Cox K, Grinton BE, Zuberi SM, Kivity S, Afawi Z, Straussberg R, Berkovic SF, Scheffer IE, Mulley JC. Heron SE, et al. J Med Genet. 2007 Dec;44(12):791-6. doi: 10.1136/jmg.2007.051938. Epub 2007 Aug 3. J Med Genet. 2007. PMID: 17675531 Free PMC article.

8

Andreas Rett and benign familial neonatal convulsions revisited.

Zimprich F, Ronen GM, Stögmann W, Baumgartner C, Stögmann E, Rett B, Pappas C, Leppert M, Singh N, Anderson VE. Zimprich F, et al. Neurology. 2006 Sep 12;67(5):864-6. doi: 10.1212/01.wnl.0000234066.46806.90. Neurology. 2006. PMID: 16966552

9

Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).

Bassi MT, Balottin U, Panzeri C, Piccinelli P, Castaldo P, Barrese V, Soldovieri MV, Miceli F, Colombo M, Bresolin N, Borgatti R, Taglialatela M. Bassi MT, et al. Neurogenetics. 2005 Dec;6(4):185-93. doi: 10.1007/s10048-005-0012-2. Epub 2005 Oct 19. Neurogenetics. 2005. PMID: 16235065 Free article.

10

A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.

Borgatti R, Zucca C, Cavallini A, Ferrario M, Panzeri C, Castaldo P, Soldovieri MV, Baschirotto C, Bresolin N, Dalla Bernardina B, Taglialatela M, Bassi MT. Borgatti R, et al. Neurology. 2004 Jul 13;63(1):57-65. doi: 10.1212/01.wnl.0000132979.08394.6d. Neurology. 2004. PMID: 15249611

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