Publications by authors named "Hande Caglayan"

Claim this Profile

Mentions over time

Mentions by platform

Video Views

282

Total Likes

141

Extended Reach

294,558

Social Features

65
E
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori, S Hande Caglayan

medRxiv· September 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes.
Özlem Yalçın Çapan, Zuhal Yapıcı, Mehmet Özbil, Hande S Çağlayan

Seizure· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Developmental and epileptic encephalopathy 82 (DEE82) with novel compound heterozygous mutations of GOT2 gene.
Özlem Yalçın Çapan, Dilşad Türkdoğan, Sertaç Atalay, Hande S Çağlayan

Seizure· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies.
Johanna Krüger, Julian Schubert, Josua Kegele, Audrey Labalme, Miaomiao Mao, Hande Caglayan

EBioMedicine· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
Sathiya N Manivannan, Jolien Roovers, Noor Smal, Candace T Myers, Dilsad Turkdogan, Hande S Caglayan

Brain· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Possible role of skeletal muscle mutation in apnea during seizure.
Dilşad Türkdoğan, Emma Matthews, Sunay Usluer, Aslı Gündoğdu, Kayıhan Uluç

Epilepsia Open· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
Herbert Schulz, Ann-Kathrin Ruppert, Federico Zara, Francesca Madia, Michele Iacomino, Hande Caglayan

Epilepsia· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.
Patrick May, Simon Girard, Merle Harrer, Dheeraj R Bobbili, Julian Schubert, Hande Caglayan

Lancet Neurol· August 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo variants in neurodevelopmental disorders with epilepsy.
Henrike O Heyne, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Caglayan

Nat Genet· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.
Ergul Berber, Mehmet Ozbil, Christine Brown, Zafer Baslar, S Hande Caglayan

Blood Transfus· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE).
Sunay Usluer, Melek Aslı Kayserili, Aslı Gündoğdu Eken, Uluc Yiş, Costin Leu

Eur J Paediatr Neurol· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Silvia Masnada, Ulrike B S Hedrich, Elena Gardella, Julian Schubert, Charu Kaiwar, Hande S Caglayan

Brain· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies.
Katrine Johannesen, Carla Marini, Siona Pfeffer, Rikke S Møller, Thomas Dorn, Hande Caglayan

Neurology· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.
Cyril Mignot, Celina von Stülpnagel, Caroline Nava, Dorothée Ville, Damien Sanlaville

J Med Genet· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations.
Sunay Usluer, Seda Salar, Mutluay Arslan, Uluç Yiş, Bülent Kara

Seizure· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pitfalls in genetic testing: the story of missed SCN1A mutations.
Tania Djémié, Sarah Weckhuysen, Sarah von Spiczak, Gemma L Carvill, Johanna Jaehn, Hande S Caglayan

Mol Genet Genomic Med· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Hande S Caglayan

Nat Genet· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.
Arvid Suls, Johanna A Jaehn, Angela Kecskés, Yvonne Weber, Sarah Weckhuysen, Hande S Caglayan

Am J Hum Genet· November 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A common VWF exon 28 haplotype in the Turkish population.
Ergul Berber, Funda Pehlevan, Mehmet Akin, Ozlem Yalcin Capan, Kaan Kavakli

Clin Appl Thromb Hemost· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel mutation in the sodium channel α1 subunit gene in a child with Dravet syndrome in Turkey.
Mutluay Arslan, Uluç Yiş, Hande Cağlayan, Rıdvan Akin

Neural Regen Res· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Double trouble: Duchenne muscular dystrophy and hemophilia.
Muge Gokce, Fatma Gümrük, Göknur Haliloğlu, Esra Serdaroğlu, Hande Cağlayan

Pediatr Blood Cancer· March 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Hum Mol Genet· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Presentation of an unusual patient with Lafora disease.
Selim Gökdemir, Hande Cağlayan, Meral Kızıltan, Naci Karaağaç, Cem Leblebici

Epileptic Disord· March 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.

Epilepsia· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis