- Q1 7
- Q2 6
- Q3 4
- Q4 5
Academician
MUHSİN ELMAS
DOÇENT
İSTANBUL MEDİPOL ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Research topics OpenAlex
- Genetic Neurodegenerative Diseases2
- Genetics and Neurodevelopmental Disorders2
- Connective tissue disorders research1
- Inflammasome and immune disorders1
- Lysosomal Storage Disorders Research1
- Neurogenetic and Muscular Disorders Research1
- Metabolism and Genetic Disorders1
- Trypanosoma species research and implications1
- Bone and Dental Protein Studies1
- RNA modifications and cancer1
- Carbohydrate Chemistry and Synthesis1
- Mitochondrial Function and Pathology1
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Academic summary
YÖKSİS and OpenAlex counted separately.
Articles
40
YÖKSİS40
OpenAlex0
Projects
5
Books
1
Proceedings
39
Citation impact
OpenAlex YÖKSİS articles matched in OpenAlex: 10
h-index
4
Percentile in Türkiye: 58
Without large collaborations: h 3 · 1 papers
#222 of 572 at their university by h-index
- i10-index
- 4
- Total citations
- 199 Top 22% in Türkiye
- Per article
- 19.9
- FWCI
- 1.56 1.00 = world average
- World top 1%
- 0
- World top 10%
- 2
Most cited articles
- The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population
- The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice
h-index and citations are computed from the citation counts of this academic’s YÖKSİS articles matched in OpenAlex (not Google Scholar, WoS or Scopus). Unmatched articles are not included.
Field ranking
YÖKSİS ?-
Main field Sağlık Bilimleri Temel AlanıPoints rank #16,956/ 43,834 top 38.7%Score 12.3 journal 11.8 · OA add 0.5
- Article rank11,096/43,834
- Scopus rank22,916/43,834
- WoS rank22,731/43,834
- YÖKSİS40
- Scopus5
- WoS5
-
Side field Tıbbi GenetikPoints rank #136/ 280 top 48.6%Score 12.3 journal 11.8 · OA add 0.5
- Article rank93/280
- Scopus rank174/280
- WoS rank173/280
- YÖKSİS40
- Scopus5
- WoS5
Index quartiles
?- Q1 4
- Q2 0
- Q3 6
- Q4 11
3 articles
- Top 1% 0
- Top 10% 2
- Avg 55.8%
- n 10
Other counts
Scopus (SJR)
- YÖKSİS rows 23
WoS (JCR)
- YÖKSİS rows 22
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Journals with publications
29 journals
- 1658-807X 6
- Journal of Pediatric Genetics 3
- 1302-4612 2
- American Journal of Human Genetics 2
- Egyptian Journal of Medical Human Genetics 2
- 0137-7183 1
- 1301-1987 1
- 2149-3189 1
- 2155-9627 1
- 2458-8733 1
- 2548-0316 1
- 2574-1241 1
- 2582-1091 1
- 2643-3885 1
- Brain and Development 1
- Clinical Dysmorphology 1
- Clinical Medicine Insights: Case Reports 1
- Eklem Hastaliklari ve Cerrahisi 1
- Functional and Integrative Genomics 1
- Indian Journal of Human Genetics 1
- International Journal of Surgery Case Reports 1
- Journal of Indian Association of Pediatric Surgeons 1
- Journal of Molecular Neuroscience 1
- Journal of the American Academy of Dermatology 1
- Meta Gene 1
- Molecular Biology Reports 1
- Molecular Syndromology 1
- Movement Disorders 1
- Turkiye Klinikleri Journal of Medical Sciences 1
Article list
- 2022 Neurodevelopment and Genetic Evaluation of Sotos Syndrome Cases with a Novel Mutation: a Single-Center Experience YÖKSİS SJR Q2 JCR Q3
- 2022 Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium YÖKSİS SJR Q2 JCR Q3 OpenAlex 74.7%
- 2022 CDH1 Gene Expression Alterations in Prostate Cancer Cell Lines After DAC And TSA Applications YÖKSİS
- 2022 Genetic and Clinical Approach To Microcephaly: A 5-Year Single Center Experience YÖKSİS SJR Q1 JCR Q4
- 2022 A female case of 5,10-methenyltetrahydrofolate synthetase deficiency with novel neuro-imaging abnormalities YÖKSİS SJR Q2 JCR Q3
- 2022 The road from mutation to next generation phenotyping: contribution of deep learning technology (Face2Gene) to diagnosis neurofibromatosis type 1 YÖKSİS TR Index
- 2021 High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 95.3%
- 2021 The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice YÖKSİS SJR Q1 JCR Q1 OpenAlex 73.7%
- 2021 Genotype to Phenotype: Identification of Mucopolysaccharidosis Type IIIB (Sanfilippo's B) Case Using Whole Exome Sequencing YÖKSİS SJR Q1 JCR Q4 OpenAlex 42.2%
- 2021 A Rare De Novo Reciprocal Translocation 46,XX,rec(7;13)(p22;q32) Karyotype YÖKSİS
- 2021 A Rare De Novo Robertsonian Translocation 45, XX, rob (13;13) (q10; q10) Karyotype Carrying in a Normal Woman; But Recurrent Abortions YÖKSİS
- 2021 Miyotonik distrofi hastalarının ctg tekrar sayıları ile genotip ve klinik bulguların değerlendirilmesi: Tek merkez deneyimi YÖKSİS SJR Q4 JCR Q4
- 2021 Afyonkarahisar bölgesinde ailesel akdeniz ateşli çocukların demografik, klinik, laboratuvar ve genetik özelliklerinin değerlendirilmesi YÖKSİS
- 2021 Down sendromlu olgularda prenatal bulgular YÖKSİS OpenAlex 9.6%
- 2020 Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience YÖKSİS SJR Q3 JCR Q4
- 2020 Investigation of clinical and genetic data of pectus excavatum in dysmorphological children: a single-center experience YÖKSİS TR Index
- 2020 Association of vitamin D level and CYP27B1 gene polymorphism with multiple sclerosis in Turkish population YÖKSİS OpenAlex 46.8%
- 2020 Two different homozygous mutations in two Turkish siblings: DGUOK and HPS5 YÖKSİS OpenAlex 56.6%
- 2020 Understanding What You Have Found: A Family With a Mutation in the LAMA1 Gene With Literature Review YÖKSİS SJR Q4 JCR Q3
- 2020 Spor eğitimi alan kişilerin eklem hipermobilitesi, yaşam kalitesi ve sosyodemografik verilerinin araştırılması: prospektif randomize kontrollü çalışma YÖKSİS