Volume 38, Issue 4, 2024

 

Editorial

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Tribute to Dr. William L. Pak and the origins of the Cold Spring Harbor summer course on Drosophila neurobiology

Chun-Fang Wu

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The Origins of the Cold Spring Harbor Laboratory Summer Course on the Neurobiology of Drosophila

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The initial years of the Cold Spring Harbor Laboratory summer course on the neurobiology of Drosophila

W. L. Pak

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Memoir of the early years of the CSHL summer Drosophila neurobiology course: 1984-1985

Ralph J. Greenspan

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Tributes to Bill Pak

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Special section in honor of William L. Pak, a neurogenetics pioneer

Barry Ganetzky

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A tribute to Bill Pak, unsung hero of neurogenetics

Barry Ganetzky

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The pioneering use of the PDA phenotype by Bill Pak for screening a network of phototransduction genes and the associated signaling pathways

Baruch Minke

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Tribute to Dr. William L. Pak

Hiroyuki Matsumoto

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A memorial piece of my experience with Bill Pak

Mamiko Ozaki

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In honor of Bill Pak: my journey to the discovery of a rhodopsin gene

Joseph E. O’Tousa

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Personal essay of a rookie’s journey with Bill Pak and his legacy: tales and perspectives on PI-PLC, NorpA and cyclophilin, NinaA - William L. Pak, PhD., 1932–2023: in memoriam

Paulo A. Ferreira

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Bill Pak: reflections on mentoring

Martin G. Burg

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Enthusiasm meets opportunity: in memoriam of William L. Pak, 1932–2023

Randall Shortridge

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My recollections of the good old days in the Pak lab

Chun-Fang Wu

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Brief Report

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A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in GARS1

Dora Varvara, Serena Lattante, Stefania Magri, Francesca Balistreri, Francesca De Razza, Franco Taroni & Salvatore Mauro

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Original Research Articles

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Clinical application of whole-exome sequencing analysis in childhood epilepsy

Meral Gavaz, Elif S. Aslan & Selahattin Tekeş

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The roles of blur and eye convergence in distance estimation in larval zebrafish

Biswadeep Khan & Julie Lee Semmelhack

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Volume 38, Issue 3, 2024

 

Review Articles

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Neurobiology of egg-laying behavior in Drosophila: neural control of the female reproductive system

Mehrnaz Afkhami

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Oncogenic roles of long non-coding RNAs in essential glioblastoma signaling pathways

Mina Lashkarboloki, Amin Jahanbakhshi, Seyed Javad Mowla, Hassan Bjeije & Bahram M. Soltani

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Clinical potential of epigenetic and microRNA biomarkers in PTSD

Nathan J. Wellington, Ana P. Boucas, Jim Lagopoulos & Anna V. Kuballa

 

Original Research Articles

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Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy

Nilgun Karasu, Hamit Acer, Hilal Akalin, Burcu Turkgenc, Mikail Demir, Izem Olcay Sahin, Nuriye Gokce, Ayten Gulec, Asli Ciplakligil, Ayse Caglar Sarilar, Isa Cuce, Hakan Gumus, Huseyin Per, Mehmet Canpolat & Munis Dundar

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Epilepsy genetics in the paediatric population of the Eastern Anatolia region of Turkey

Oğuzhan Yarali, Özge Beyza Gündoğdu Öğütlü, Serdar Saritaş, Mustafa Can Guler, Filiz Keskin & Ayberk Türkyilmaz

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Targeted deletion of olfactory receptors in D. melanogaster via CRISPR/Cas9-mediated LexA knock-in

Runqi Zhang, Renny Ng, Shiuan-Tze Wu & Chih-Ying Su

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​Volume 38, Issue 2, 2024

 

Original Research Articles

 

Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy

Shivani Sharma, Anita Mahadevan, Gayathri Narayanappa, Monojit Debnath, Periyasamy Govindaraj, Sumanth Shivaram, Doniparthi V. Seshagiri, Ramesh Siram, Akhilesh Shroti, Parayil S. Bindu, Yasha T. Chickabasaviah, Arun B. Taly & Madhu Nagappa

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SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause

Annabelle Arlt, Esra Akova-Öztürk, Anja Schirmacher, Bernhard Schlüter, Stephan Rust, Gerd Meyer zu Hörste, Heinz Wiendl & Sarah Wiethoff

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Brief Report

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Carbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation

Jasmine Policherla, Fatema J. Serajee, Salman Rashid & A. H. M. Mahbubul Huq

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Volume 38, Issues 1, 2024

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Review Article

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Meta-analysis of the association between C9orf72 repeats and neurodegeneration diseases

Pingfei Jin, Yong Li & Yao Li

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Original Research Article

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Global research landscape on the contribution of de novo mutations to human genetic diseases over the past 20 years: bibliometric analysis

Jing Guan, Xiaonan Wu, Jiao Zhang, Jin Li, Hongyang Wang & Qiuju Wang

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Brief Report

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Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder

Asal Asghari Sarfaraz, Neda Jabbarpour, Mortaza Bonyadi & Mohammad Khalaj-Kondory​