Journal of Neurogenetics, Volume 31, Issue 1-2 (2017)

Browse this journal
Sample our Medicine, Dentistry, Nursing & Allied Health journals, sign in here to start your FREE access for 14 days

Journal of Neurogenetics, Volume 31, Issue 1-2 (2017)

See all volumes and issues
Vol 37, 2023 Vol 36, 2022 Vol 35, 2021 Vol 34, 2020 Vol 33, 2019 Vol 32, 2018 Volume 31, 2017 Vol 30, 2016 Vol 29, 2015 Vol 28, 2014 Vol 27, 2013 Vol 26, 2012 Vol 25, 2011 Vol 24, 2010 Vol 23, 2009 Vol 22, 2008 Vol 21, 2007 Vol 20, 2006 Vol 19, 2005 Vol 18, 2004 Vol 17, 2003 Vol 16, 2002 Vol 15, 2001 Vol 14, 2000 Vol 13, 1999-2000 Vol 12, 1998 Vol 11, 1996-1997 Vol 10, 1995-1996 Vol 9, 1993-1995 Vol 8, 1992-1993 Vol 7, 1990-1991 Vol 6, 1989-1990 Vol 5, 1989 Vol 4, 1987 Vol 3, 1986 Vol 2, 1985 Vol 1, 1983-1984
Download citations Download PDFs Download issue

Review

Review
Gene polymorphisms associated with temperament
Xiaoyan Qiu, Graeme B. Martin & Dominique Blache
Pages: 1-16
Published online: 16 May 2017
AbstractforGene polymorphisms associated with temperament | Full Text | References | PDF (1.6 MB)
  • 369 Views
  • 10 CrossRef citations
  • 0Altmetric

Short Communication

Rapid Communication
Drift diffusion model of reward and punishment learning in rare alpha-synuclein gene carriers
Ahmed A. Moustafa, Szabolcs Kéri, Bertalan Polner & Corey White
Pages: 17-22
Published online: 20 Mar 2017
AbstractforDrift diffusion model of reward and punishment learning in rare alpha-synuclein gene carriers | Full Text | References | PDF (879.4 KB)
  • 227 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Novel PNKP mutation in siblings with ataxia-oculomotor apraxia type 4
Nicoline Schiess, David S. Zee, Khurram A. Siddiqui, Miklos Szolics & Ayman W. El-Hattab
Pages: 23-25
Published online: 29 May 2017
AbstractforNovel PNKP mutation in siblings with ataxia-oculomotor apraxia type 4 | Full Text | References | PDF (563.8 KB) | Supplemental
  • 333 Views
  • 14 CrossRef citations
  • 0Altmetric
Rapid Communication
A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysis
Huma Tariq, Shahid Mukhtar & Sadaf Naz
Pages: 26-29
Published online: 13 May 2017
AbstractforA novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysis | Full Text | References | PDF (745.2 KB)
  • 253 Views
  • 9 CrossRef citations
  • 0Altmetric

Original Research Article

Article
Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype
Fanggeng Zou, Kirsty McWalter, Lindsay Schmidt, Amy Decker, Jonathan D. Picker, Sharyn Lincoln, David A. Sweetser, Lauren C. Briere, Chellamani Harini, Members of the Undiagnosed Diseases Network, Eric Marsh, Livija Medne, Raymond Y. Wang, Karen Leydiker, Andrew Mower, Gepke Visser, Inge Cuppen, Koen L. van Gassen, Jasper van der Smagt, Adeel Yousaf, Michael Tennison, Anita Shanmugham, Elizabeth Butler, Gabriele Richard & Dianalee McKnight
Pages: 30-36
Published online: 02 May 2017
AbstractforExpanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype | Full Text | References | PDF (1.4 MB)
  • 439 Views
  • 11 CrossRef citations
  • 0Altmetric
Article
Astroglial transcriptome dysregulation in early disease of an ALS mutant SOD1 mouse model
Sean J. Miller, Ping-wu Zhang, Jenna Glatzer & Jeffrey D. Rothstein
Pages: 37-48
Published online: 25 Dec 2016
AbstractforAstroglial transcriptome dysregulation in early disease of an ALS mutant SOD1 mouse model | Full Text | References | PDF (2.1 MB) | Supplemental
  • 3369 Views
  • 12 CrossRef citations
  • 0Altmetric
Open Access
Article
Quantitative analysis of visually induced courtship elements in Drosophila subobscura
Tomohiro Higuchi, Soh Kohatsu & Daisuke Yamamoto
Pages: 49-57
Published online: 19 Feb 2017
AbstractforQuantitative analysis of visually induced courtship elements in Drosophila subobscura | Full Text | References | PDF (1.4 MB)
  • 269 Views
  • 4 CrossRef citations
  • 0Altmetric

Explore articles

Explore the most recently published articles

Carbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation
Jasmine Policherla et al.
Brief Report | Published online: 15 Jul 2024
Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy
Shivani Sharma et al.
Article | Published online: 8 Jul 2024
Bill Pak: reflections on mentoring
Martin G. Burg
Comment | Published online: 8 Jul 2024
SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause
Annabelle Arlt et al.
Article | Published online: 8 Jul 2024
Open Access
View all latest articles