Akademisyen
SERDAR CEYLANER
Profesör
Lokman Hekim Üniversitesi Tıp Fakültesi Dahili Tıp Bilimleri Bölümü
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Atıf etkisi
OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 93 + YÖKSİS · ortak yazar kaydı: 115- i10-indeks
- 71
- Toplam atıf
- 1.978 Türkiye’de üst %3,4
- Makale başına
- 9,5
- FWCI
- 0,71 1,00 = dünya ortalaması
- Dünyada üst %1
- 0
- Dünyada üst %10
- 9
En çok atıf alan makaleleri
Nasıl hesaplanır?
h-indeks ve atıflar, bu akademisyenin YÖKSİS makalelerinden OpenAlex’te eşleşenlerin atıf sayılarından hesaplanır (Google Scholar, WoS veya Scopus değildir). Eşleşmeyen makalelerin atıfı dahil değildir. Ortak yazarların YÖKSİS kayıtlarında bu akademisyenin YÖK kimliğiyle etiketlenen 115 makale (729 atıf) yalnızca atıf, h-indeks ve i10 hesabına katılır; makale sayıları, yüzdelik dilimler ve sıralamalar kendi YÖKSİS listesinden hesaplanır. OpenAlex yazar profilindeki h-indeks: 23.
Alan sıralaması
YÖKSİS ?-
Ana dal Sağlık Bilimleri Temel AlanıPuan sırası #1.061/ 39.749 üst %2,7 Üniversitede #8/ 264Puan 75,8 dergi 74,8 · OA ek 1
- Makale sırası2.412/39.749
- Scopus sırası824/39.749
- WoS sırası770/39.749
- YÖKSİS97
- Scopus92
- WoS93
-
Yan dal Tıbbi GenetikPuan sırası #15/ 250 üst %6,0 Üniversitede #1/ 2Puan 75,8 dergi 74,8 · OA ek 1
- Makale sırası26/250
- Scopus sırası13/250
- WoS sırası11/250
- YÖKSİS97
- Scopus92
- WoS93
Dizinler ve atıf yüzdelikleri
?Diğer sayımlar
Scopus (SJR)
- YÖKSİS satırı 92
WoS (JCR)
- YÖKSİS satırı 92
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Yayını olan dergiler
55 dergi
- Journal of Pediatric Endocrinology and Metabolism 17
- American Journal of Medical Genetics, Part A 6
- JCRPE Journal of Clinical Research in Pediatric Endocrinology 6
- Prenatal Diagnosis 6
- Turkish Journal of Pediatrics 6
- Journal of Pediatric Research 3
- Brain and Development 2
- Clinical Dysmorphology 2
- Journal of Child Neurology 2
- Taiwanese Journal of Obstetrics and Gynecology 2
- ISSN 1292-3140 1
- ISSN 1302-8723 1
- ISSN 2090-6668 1
- ISSN 2919-4042 1
- 7666393 1
- Acta Orthopaedica et Traumatologica Turcica 1
- American Journal of Obstetrics and Gynecology 1
- Anatolian Journal of Cardiology 1
- Annals of Indian Academy of Neurology 1
- Australian and New Zealand Journal of Obstetrics and Gynaecology 1
- Brain 1
- Clinica Chimica Acta 1
- Clinical Case Reports (discontinued) 1
- Clinical Genetics 1
- Clinical Pediatrics 1
- Congenital Anomalies (discontinued) 1
- Current Opinion in Biotechnology 1
- Digestive Diseases and Sciences 1
- Epilepsy and Behavior Case Reports 1
- European Journal of Medical Genetics 1
- European Journal of Pediatrics 1
- Fertility and Sterility 1
- Fetal Diagnosis and Therapy 1
- Hormone Research in Paediatrics 1
- Human Fertility 1
- Human Mutation 1
- International Journal of Diabetes in Developing Countries 1
- International Journal of Gynecology and Obstetrics 1
- Journal of Bone Oncology 1
- Journal of Genetics 1
- Journal of Investigative Dermatology 1
- Journal of Maternal-Fetal and Neonatal Medicine 1
- Journal of Obstetrics and Gynaecology 1
- Journal of Pediatric and Adolescent Gynecology 1
- Journal of Pediatric Orthopaedics Part B 1
- Journal of Pediatric Surgery 1
- Marmara Medical Journal 1
- Molecular Reproduction and Development 1
- Neuromuscular Disorders 1
- Pediatric Blood and Cancer 1
- Pediatric Infectious Disease Journal 1
- Pediatric Neurology 1
- Pediatrics International 1
- Transplantation Proceedings 1
- Tumori 1
Daralt
Makale listesi
- 2023 Non-Metastatic Ewing's Sarcoma Family of Tumors of Bone in Adolescents and Adults YÖKSİS SJR Q3 JCR Q3 OpenAlex 77.1%
- 2022 Vitamin D receptor gene polymorphisms in pediatric patients with leukemia-lymphoma: Does it have an impact on malignancy? YÖKSİS TR Index SJR Q4 OpenAlex 15.8%
- 2021 Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis. YÖKSİS SJR Q1 JCR Q1 OpenAlex 88.8%
- 2020 Mitochondrial membrane protein–associated neurodegeneration: A case series of six children YÖKSİS SJR Q3 JCR Q4 OpenAlex 62.0%
- 2019 Association of vitamin D receptor gene polymorphisms with osteosarcoma risk and prognosis YÖKSİS SJR Q2 JCR Q3 OpenAlex 76.4%
- 2018 Twenty-seven mutations with three novel pathologenic variants causing biotinidase deficiency: a report of 203 patients from the southeastern part of Turkey YÖKSİS SJR Q2 JCR Q3 OpenAlex 65.7%
- 2018 Siblings with Ethylmalonic Encephalopathy: Case Report YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 4.1%
- 2018 A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 1.3%
- 2018 “Double Hit” Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 4.6%
- 2018 Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty YÖKSİS TR Index SJR Q2 JCR Q3 OpenAlex üst %10 OpenAlex 91.4%
- 2018 Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I YÖKSİS OpenAlex 61.9%
- 2017 A case of Riley Ruvalcaba syndrome with a novel PTEN mutation accompanied by diffuse testicular microlithiasis and precocious puberty YÖKSİS SJR Q2 JCR Q4 OpenAlex 57.9%
- 2017 A novel mutation in the desmoplakin gene in two female siblings with a rare form of dilated cardiomyopathy: Carvajal syndrome YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 70.2%
- 2017 Improved metabolic control in tetrahydrobiopterin (BH4), responsive phenylketonuria with sapropterin administered in two divided doses vs. a single daily dose YÖKSİS SJR Q2 JCR Q4 OpenAlex 62.7%
- 2017 A novel frameshift mutation of malonyl‐CoA decarboxylase deficiency: clinical signs and therapy response of a late‐diagnosed case YÖKSİS SJR Q4 JCR Q3 OpenAlex 63.2%
- 2017 Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1 YÖKSİS SJR Q3 OpenAlex 56.0%
- 2017 Impaired glucose tolerance in fanconi-bickel syndrome: eight patients with two novel mutations YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 70.2%
- 2017 Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign YÖKSİS TR Index SJR Q2 JCR Q3
- 2017 Microcephaly and developmental delay caused by short-chain acyl-coa dehydrogenase deficiency YÖKSİS TR Index SJR Q3 JCR Q4
- 2017 The variable clinical phenotype of three patients with hepatic glycogen synthase deficiency YÖKSİS SJR Q2 JCR Q4 OpenAlex üst %10 OpenAlex 90.2%