Ali Dursun - Concepedia

Author

Ali Dursun

Also Known As

A Dursun, A. Dursun, Ali DURSUN, Ali Dursun, Ali Emre Dursun, Dursun, Ali, William Newman, Yamaç Karaboncuk, İncilay Lay

141

Publications

Citations

H-Index

106

Concepts

All Affiliations

Hacettepe University Istanbul University Aksaray University Hacettepe University Hospital Kırıkkale University

About

Ali Dursun is an author at Hacettepe University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	28	1.1K
2	Public Health	5	5	183
3	Health Sciences	2	2	281
4	Natural Sciences	2	2	30
5	Arts	1	1	23

Ali Dursun

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg, Pediatric Research NutritionMetabolic DisorderPediatric HematologyTreatment EfficacyHematology	2006	266
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction Naiara Akizu, Vincent Cantagrel, Maha S. Zaki, Nature Genetics Cell AutophagyMitophagyBiallelic MutationsCerebellar AtrophyMendelian Disorder	2015	134
Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients Hong‐Zhi Gao, Keiko Kobayashi, Ayako Tabata, Human Mutation Argininosuccinate Synthetase GeneClassical Citrullinemia PatientsGenetic DisorderGeneticsAss Mutations	2003	83
Dry Eye Related to Commonly Used New Antidepressants Emel Koçer, Abdülkadir Koçer, Mustafa Özsütçü, Journal of Clinical Psychopharmacology New AntidepressantsOphthalmologyPsychiatryMedicinePsychotropic Medication	2015	77
Newborn PKU screening in Turkey: at present and organization for future. İ Özalp, Turgay Coşkun, H. Serap Kalkanoğlu, PubMed Pkenylketonuria ScreeningPersistent HyperphenylalaninemiaNeonatologyDiagnosisScreening Program	2001	65
The molecular basis of familial hypercholesterolaemia in Turkish patients Mert Sozen, Ros Whittall, Cihan Öner, Atherosclerosis Metabolic SyndromeLipid DisorderTurkish PatientsCardiovascular DiseaseHyperlipidemia	2005	43
Mutations in the <i>G6PC3</i> gene cause Dursun syndrome Siddharth Banka, William G. Newman, Rıza Köksal Özgül, American Journal of Medical Genetics Part A Atrial Septal DefectHeart FailureDursun SyndromeGenetic DisorderGenetics	2010	39
Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screening Mehmet Ali Karaca, Rıza Köksal Özgül, Özlem Ünal, European Journal of Pediatrics Genetic TestingTurkish PatientsFamily ScreeningGenetic DisorderMedicine	2015	37
A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutation Ali Dursun, Dilek Yalnızoğlu, Omer F. Gerdan, Clinical Dysmorphology Developmental AnomalyRare DiseasesMendelian DisorderFamily MembersGenetic Disorder	2016	36
Homozygous <i>GNAL</i> mutation associated with familial childhood-onset generalized dystonia Ikuo Masuho, Mingyan Fang, Chunyu Geng, Neurology Genetics	2016	35

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