Ayça Aykut - Concepedia

Author

Ayça Aykut

Also Known As

A Aykut, A. Aykut, Aleksandra Jezela-Stanek, Ayca AYKUT, Ayca Aykut, Ayça AYKUT, Ayça Aykut, Ayça DURMUŞ AYKUT, Ayça Durmus Aykut

147

Publications

929

Citations

H-Index

Concepts

All Affiliations

Ege University Dokuz Eylül University Ankara University Izmir University Sağlık Bilimleri Üniversitesi

About

Ayça Aykut is an author at Ege University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	17	406
2	Public Health	3	3	99
3	Engineering	1	1	14
4	Allergy	1	1	24
5	Biostatistics	1	1	22

Ayça Aykut

Publications

714

Citations

H-Index

Page 1

	Year	Citations
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss Hüseyin Önay, Ayça Aykut, Güney Bademci, PLoS ONE GeneticsGenetic EpidemiologyDisease Gene IdentificationGenomicsMendelian Disorder	2015	64
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome Esther Pohl, Ayça Aykut, Filippo Beleggia, Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyHypofunctional Pax1 Mutation	2013	60
Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice Afrooz Rashnonejad, Gholamhossein Amini Chermahini, Cumhur Gündüz, Molecular Therapy	2019	55
Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes Aslı Ece Solmaz, Hüseyin Önay, Ayça Aykut, European Journal of Medical Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsBardet Biedl Syndrome	2015	45
Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics Ayça Aykut, Samim Özen, Damla Gökşen, European Journal of Pediatrics ObesityMetabolic SyndromeChildhood ObesityMetabolic DisorderMelanocortin 4	2020	37
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism Asude Durmaz, Ayça Aykut, Samim Özen, Journal of Clinical Research in Pediatric Endocrinology	2020	33
Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome Emin Karaca, Ayça Aykut, Biray Ertürk, Balkan Medical Journal	2017	26
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages Necil Kütükçüler, Ayça Aykut, Neslihan Edeer Karaca, Scandinavian Journal of Immunology Family MedicineImmunodeficienciesGeneticsImmunologyPathology	2018	24
Prenatal Evaluation of MicroRNA Expressions in Pregnancies with Down Syndrome Biray Ertürk, Emin Karaca, Ayça Aykut, BioMed Research International	2016	23
Biallelic TOR1A mutations cause severe arthrogryposis: A case requiring reverse phenotyping Ayça Aykut, Özgür Çoğulu, Ferda Özkınay European Journal of Medical Genetics Biallelic Tor1a MutationsGenetic DisorderGeneticsPathologySevere Arthrogryposis	2018	22

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