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Year Number of Results
1974 1
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1979 1
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1989 1
1990 3
1991 2
1992 2
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1999 3
2000 4
2001 3
2002 5
2003 2
2004 3
2005 4
2006 5
2007 4
2008 2
2009 2
2010 1
2011 3
2012 5
2013 4
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2019 6
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91 results

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Page 1
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell Models.
Houdayer C, Phillips AM, Chabbert M, Bourreau J, Maroofian R, Houlden H, Richards K, Saadi NW, Dad'ová E, Van Bogaert P, Rupin M, Keren B, Charles P, Smol T, Riquet A, Pais L, O'Donnell-Luria A, VanNoy GE, Bayat A, Møller RS, Olofsson K, Jamra RA, Syrbe S, Dasouki M, Seaver LH, Sullivan JA, Shashi V, Alkuraya FS, Poss AF, Spence JE, Schnur RE, Forster IC, Mckenzie CE, Simons C, Wang M, Snell P, Kothur K, Buckley M, Roscioli T, Elserafy N, Dauriat B, Procaccio V, Henrion D, Lenaers G, Colin E, Verbeek NE, Van Gassen KL, Legendre C, Bonneau D, Reid CA, Howell KB, Ziegler A, Legros C. Houdayer C, et al. Among authors: forster ic. Ann Neurol. 2025 Sep;98(3):573-589. doi: 10.1002/ana.27277. Epub 2025 Jun 5. Ann Neurol. 2025. PMID: 40468825 Free PMC article.
Mono and biallelic variants in HCN2 cause severe neurodevelopmental disorders.
Houdayer C, Phillips AM, Chabbert M, Bourreau J, Maroofian R, Houlden H, Richards K, Saadi NW, Dad'ová E, Van Bogaert P, Rupin M, Keren B, Charles P, Smol T, Riquet A, Pais L, O'Donnell-Luria A, VanNoy GE, Bayat A, Møller RS, Olofsson K, Abou Jamra R, Syrbe S, Dasouki M, Seaver LH, Sullivan JA, Shashi V, Alkuraya FS, Poss AF, Spence JE, Schnur RE, Forster IC, Mckenzie CE, Simons C, Wang M, Snell P, Kothur K, Buckley M, Roscioli T, Elserafy N, Dauriat B, Procaccio V, Henrion D, Lenaers G, Colin E, Verbeek NE, Van Gassen KL, Legendre C, Bonneau D, Reid CA, Howell KB, Ziegler A, Legros C. Houdayer C, et al. Among authors: forster ic. medRxiv [Preprint]. 2024 Mar 22:2024.03.19.24303984. doi: 10.1101/2024.03.19.24303984. medRxiv. 2024. PMID: 38562733 Free PMC article. Preprint.
Retinal Dysfunction in a Mouse Model of HCN1 Genetic Epilepsy.
Zhao D, Pinares-Garcia P, McKenzie CE, Bleakley LE, Forster IC, Wong VHY, Nguyen CTO, Scheffer IE, Reid CA, Bui BV. Zhao D, et al. Among authors: forster ic. J Neurosci. 2023 Mar 22;43(12):2199-2209. doi: 10.1523/JNEUROSCI.1615-22.2022. Epub 2023 Feb 22. J Neurosci. 2023. PMID: 36813574 Free PMC article.
Corrigendum to "Biophysical analysis of an HCN1 epilepsy variant suggests a critical role for S5 helix Met-305 in voltage sensor to pore domain coupling" [Prog. Biophys. Mol. Biol. 166 (2021) 156-172].
Hung A, Forster IC, Mckenzie CE, Berecki G, Petrou S, Kathirvel A, Soh MS, Reid CA. Hung A, et al. Among authors: forster ic. Prog Biophys Mol Biol. 2022 Aug;172:90. doi: 10.1016/j.pbiomolbio.2022.05.003. Epub 2022 May 21. Prog Biophys Mol Biol. 2022. PMID: 35606165 No abstract available.
Impaired Color Recognition in HCN1 Epilepsy: A Single Case Report.
Mckenzie CE, Ho CJ, Forster IC, Soh MS, Phillips AM, Chang YC, Scheffer IE, Reid CA, Tsai MH. Mckenzie CE, et al. Among authors: forster ic. Front Neurol. 2022 Mar 10;13:834252. doi: 10.3389/fneur.2022.834252. eCollection 2022. Front Neurol. 2022. PMID: 35359652 Free PMC article.
91 results