Volume 31, 2017

Table of Contents

Latest Issue:

Volume 31, Issue 4, 2017

Special Issue: Neurogenetics in Spain

Special Issue Articles

Editorial

Neurogenetics in Spain

Alberto Ferrús (Guest Editor

Original Research Articles

Orb2 as modulator of Brat and their role at the neuromuscular junction

Elena Santana & Sergio Casas-Tintó

Overexpression of Drosophila frataxin triggers cell death in an iron-dependent manner

Oliver Edenharter, Janik Clement, Stephan Schneuwly, & Juan A. Navarro

Review Articles

The pigmented epithelium, a bright partner against photoreceptor degeneration

Joaquín Letelier, Paola Bovolenta & Juan R. Martínez-Morales

Aberrant Wnt signaling: a special focus in CNS diseases

Mercedes Arnés & Sergio Casas Tintó

Local translation of the Down syndrome cell adhesion molecule (DSCAM) mRNA in the vertebrate central nervous system

María Luz Montesinos

Untangling the wiring of the Drosophila visual system: developmental principles and molecular strategies

Haritz Plazaola-Sasieta, Alejandra Fernández-Pineda, Qi Zhu & Marta Morey

Neurogenetics of Drosophila circadian clock: expect the unexpected

Patricia Jarabo & Francisco A. Martin

Molecular bases of anorexia nervosa, bulimia nervosa and binge eating disorder: shedding light on the darkness

Germán Cuesto, Claude Everaerts, Leticia G. León, & Angel Acebes

Novel genetic approaches to behavior in Drosophila

Fernando Martín & Esther Alcorta

Interaction of sex chromosome complement, gonadal hormones and neuronal steroid synthesis on the sexual differentiation of mammalian neurons

Maria Julia Cambiasso, Carla Daniela Cisternas, Isabel Ruiz-Palmero, Maria Julia Scerbo, Maria Angeles Arevalo, Iñigo Azcoitia & Luis M. Garcia-Segura


Computational prediction of the phenotypic effects of genetic variants: basic concepts and some application examples in Drosophila nervous system genes

Alejandro Sánchez-Gracia, Sara Guirao-Rico, Silvia Hinojosa-Alvarez & Julio Rozas

Regular Submissions

Letters to the Editor

RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing

Cassie L. Albury, Zachary Gerring, Lyn R. Griffiths, Dale R. Nyhol & Astrid J. Rodriguez-Acevedo

Response from Original Authors - RE: Six novel rare nonsynonymous mutations for migraine without aura identified by exome sequencing

Xiao-Ping Wang, Zhi-Xiang Xu, Xiao-Jing Sun & Xingguang Luo

Original Research Articles

Generation and characterization of new alleles of quiver (qvr) that encodes an extracellular modulator of the Shaker potassium channel

Hongyu Ruan, Atsushi Ueda, Xiaomin Xing, Xuxuan Wan, Benjamin Strub, Spencer Mukai, Kaan Certel, David Green, Kyle Belozerov, Wei-Dong Yao, Wayne Johnson, Jim Jung-Ching Lin, Arthur J. Hilliker & Chun-Fang Wu

Overexpression of U1 snRNA induces decrease of U1 spliceosome function associated with Alzheimer’s disease

Zhi Cheng, Yingchun Shang, Shan Gao & Tao Zhang

Association of transcription factor 4 (TCF4) gene mRNA level with schizophrenia, its psychopathology, intelligence and cognitive impairments

Fatemeh Alizadeh, Javad Tavakkoly-Bazzaz, Ali Bozorgmehr, Asa’ad Azarnezhad, Mina Tabrizi & Esmaeil Shahsavand Ananloo

Corrigendum

Correction to: Albury et al., RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing

Volume 31, Issue 3, 2017

Special Issue: Zebrafish: From Genes and Neurons to Circuits, Behavior and Disease

Special Issue Articles

Editorial

Zebrafish: from genes and neurons to circuits, behavior and disease

Guest Editors Anand Chandrasekhar, Su Guo, Ichiro Masai, & Teresa Nicolson; Editor-in-Chief Chun-Fang Wu

Review Articles

The power of projectomes: genetic mosaic labeling in the larval zebrafish brain reveals organizing principles of sensory circuits

Estuardo Robles

Genetic approaches to retinal research in zebrafish

Stephanie Niklaus & Stephan C. F. Neuhauss

Neurotoxicity of cGMP in the vertebrate retina: from the initial research on rd mutant mice to zebrafish genetic approaches

Maria Iribarne & Ichiro Masai

The genetics of hair-cell function in zebrafish

Teresa Nicolson

Light on a sensory interface linking the cerebrospinal fluid to motor circuits in vertebrate

Lydia Djenoune & Claire Wyart

Original Research Articles

Role of branchiomotor neurons in controlling food intake of zebrafish larvae

James R. Allen, Kiran D. Bhattacharyya, Emilia Asante, Badr Almadi, Kyle Schafer, Jeremy Davis, Jane Cox, Mark Voigt, John A. Viator,

& Anand Chandrasekhar

Heritable natural variation of an anxiety-like behavior in larval zebrafish

Mahendra Wagle , Juliana Nguyen, Shinwoo Lee, Noah Zaitlen, & Su Guo

Regular Submissions

Short Communication

Primary familial brain calcifications linked with a novel SLC20A2 gene mutation in a Chinese family

Tao-Mian MiWei MaoYan-Ning CaiCai-Xia YangChao-Dong WangEr-He XuHui Zhang, & Piu Chan

Original Articles

Obsessive–compulsive disorder, which genes? Which functions? Which pathways? An integrated holistic view regarding OCD and its complex genetic etiology

Ali BozorgmehrMohammad Ghadirivasfi, & Esmaeil Shahsavand Ananloo

LGMD2E is the most common type of sarcoglycanopathies in the Iranian population

Afagh Alavi, Sara Esmaeili, Yalda Nilipour, Shahriar Nafissi, Seyed Hasan Tonekaboni, Gholamreza Zamani, Mahmoud Reza Ashrafi, Kimia Kahrizi, Hossein Najmabadi, & Fatemeh Jazayeri

Loss of control over the ethanol consumption: differential transcriptional regulation in prefrontal cortex

Carolina de Paiva Lima, Daniel Almeida da Silva e Silva, Samara Damasceno, Andrea Frozino Ribeiro, Cristiane S. Rocha, Alexandre H. Berenguer de Matos, Diego Correia, Roseli Boerngen-Lacerda, & Ana Lúcia Brunialti Godard

Volume 31, Issue 1-2, 2017

Review

Gene polymorphisms associated with temperament

Xiaoyan Qiu, Graeme B. Martin, & Dominique Blache

Short Communications

Drift diffusion model of reward and punishment learning in rare alpha-synuclein gene carriers

Ahmed A. Moustafa, Szabolcs Kéri, Bertalan Polner, & Corey White

Novel PNKP mutation in siblings with ataxia-oculomotor apraxia type 4

Nicoline Schiess, Davis S. Zee, Khurram A. Siddiqui, Miklos Szolics, & Ayman W. El-Hattab

A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysis

Huma Tariq, Shahid Mukthar, & Sadaf Naz

Original Research Articles

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

Astroglial transcriptome dysregulation in early disease of an ALS mutant SOD1 mouse model

Sean J. Miller, Ping-wu Zhang, Jenna Glatzer, & Jeffrey D. Rothstein

Quantitative analysis of visually induced courtship elements in Drosophila subobscura

Tomohiro Higuchi, Soh Kohatsu, & Daisuke Yamamoto

 
 

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