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Academician

EMRAH KAYGUSUZ

Doktor Öğretim Üyesi

Bilecik Şeyh Edebali Üniversitesi

Research topics OpenAlex
Articles 10 YÖKSİS 10 · OpenAlex 0 Total citations 147 h-index 6 · OpenAlex OpenAlex coverage %70 matched 7 / 10 Q1 articles 6 Scopus · WoS Q1 3 Co-authors 75 2 Turkish institutions

Citation impact

Citation counts of the articles matched in OpenAlex, citing publications from Crossref and the Stanford/Elsevier list. Sources are shown separately and never added up.

OpenAlex YÖKSİS articles matched in OpenAlex: 7 + YÖKSİS · co-author record: 2
h-index 6 Percentile in Türkiye: 60 #145 of 657 at their university by h-index
i10-index
5
Total citations
147
Top 31% in Türkiye
Per article
16.3
FWCI
1.16
1.00 = world average
World top 1%
0
World top 10%
0

Most cited articles

  1. Mutations in CKAP2L, the Human Homolog of the Mouse Radmis Gene, Cause Filippi Syndrome 2014 50 citations
  2. An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan 2020 37 citations
  3. De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway 2022 20 citations
How is this computed?

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. 2 articles (7 citations) tagged with this academic’s YÖK author id in co-authors’ YÖKSİS records count only towards citations, h-index and i10; article counts, percentiles and rankings use their own YÖKSİS list. h-index on the OpenAlex author profile: 6.

Citing publications Crossref 20 publications citing 7 DOI-bearing articles · 3 Türkiye-affiliated
  • 2019 3
  • 2020 4
  • 2021 8
  • 2022 3
  • 2025 2
  1. DOI 10.1007/s00018-025-05950-z 2025
  2. DOI 10.1093/ijlct/ctaf127 2025
  3. A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family TR Syeda Farwa Naqvi et al. · Genetic Testing and Molecular Biomarkers · 2022
  4. DOI 10.1155/2022/3769948 2022
  5. DOI 10.1002/ajmg.a.62702 2022
  6. Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ TR Ehtisham Ul Haq Makhdoom et al. · Genes · 2021
  7. Identification of a novel pathogenic variant in CKAP2L and literature review in a child with Filippi syndrome and congenital talipes equinovarus TR Taner Karakaya et al. · American Journal of Medical Genetics Part A · 2021
  8. DOI 10.3389/fped.2021.695133 2021
  9. DOI 10.3390/genes12101494 2021
  10. DOI 10.1158/0008-5472.can-20-1968 2021
  11. DOI 10.1111/dmcn.15060 2021
  12. DOI 10.3389/fcell.2021.640753 2021
  13. DOI 10.3390/genes12040594 2021
  14. DOI 10.3892/etm.2020.8522 2020
  15. DOI 10.1155/2020/3876834 2020
  16. DOI 10.3390/ijms22010197 2020
  17. DOI 10.1186/s12957-020-02042-z 2020
  18. DOI 10.1002/stem.2993 2019
  19. DOI 10.1186/s12859-019-2944-9 2019
  20. DOI 10.1097/mcd.0000000000000267 2019
Where does this list come from?

Extracted from the reference lists in Crossref’s public March 2026 data file; 20.3% of the file has been processed, so the list may be incomplete. Crossref citations are never added to or compared with the OpenAlex citation counts; the two sources have different coverage.

Works 10

YÖKSİS and OpenAlex records: index distribution, journals published in, a filterable article list and the other output types.

Indexes and citation percentiles

?
TR Index 0 articles
OpenAlex citation percentile
Top 1%0
Top 10%0
Avg · n 8 %74.3
Other counts

Scopus (SJR)

  • Excluding abstracts 7 Q1 5 Q2 1 Q3 1
  • YÖKSİS rows 9

WoS (JCR)

  • Excluding abstracts 7 Q1 3 Q2 3 Q3 1
  • YÖKSİS rows 9

Articles

Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.

10articles

Journals with publications

8 journals

Narrow down

Scopus (SJR)
Q16 Q21 Q31 Q40
WoS (JCR)
Q13 Q24 Q31 Q40
TR Index
0articles

Article list

  1. 2025 Synergistic MDM2-STAT3 Inhibition Demonstrates Strong Anti-Leukemic Efficacy in Acute Lymphoblastic Leukemia INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES DOI 10.3390/ijms26178648 YÖKSİS SJR Q1 JCR Q1 OpenAlex 79.0%
  2. 2022 De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway HUMAN GENETICS AND GENOMICS ADVANCES DOI 10.1016/j.xhgg.2022.100111 YÖKSİS SJR Q1 JCR Q2 OpenAlex 82.9%
  3. 2021 Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ Genes DOI 10.3390/genes12050731 YÖKSİS SJR Q2 JCR Q2 OpenAlex 80.6%
  4. 2021 A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome Clinical Genetics DOI 10.1111/cge.14028 2 YÖKSİS records YÖKSİS SJR Q1 JCR Q2 OpenAlex 48.8%
  5. 2021 Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state Journal of Medical Genetics DOI 10.1136/jmedgenet-2021-107769 YÖKSİS SJR Q1 JCR Q1 OpenAlex 83.8%
  6. 2020 An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan Molecular Genetics & Genomic Medicine DOI 10.1002/mgg3.1408 YÖKSİS SJR Q3 JCR Q3 OpenAlex 83.1%
  7. 2020 De novo pathogenic variants in CSNK2B cause a new intellectual disability-craniodigital syndrome distinguished from Poirier-Bienvenu neurodevelopmental syndrome EUROPEAN JOURNAL OF HUMAN GENETICS YÖKSİS SJR Q1 JCR Q2
  8. 2019 De novo mutation of CSNK2B encoding beta subunit of casein kinase 2 causes Filippi syndrome EUROPEAN JOURNAL OF HUMAN GENETICS YÖKSİS
  9. 2019 Identification of a founder mutation in Pakistani families affected with Jawad syndrome 35th Ernst Klenk Symposium in Molecular Medicine YÖKSİS
  10. 2014 Mutations in CKAP2L, the Human Homolog of the Mouse Radmis Gene, Cause Filippi Syndrome The American Journal of Human Genetics DOI 10.1016/j.ajhg.2014.10.008 YÖKSİS SJR Q1 JCR Q1 OpenAlex 87.3%

Projects 5

  1. 2021 Akut Lenfoblastik Lösemide MDM2 ve STAT3'ün Kombine Hedeflenmesinin Yeni Bir Tedavi Yaklaşımı Olarak Araştırılması -Tübitak 3501 · Tamamlandı 2021-12-01 – 2024-04-01
  2. 2012 Paradigm of the centrosomal and cell cycle regulator proteins in embryonic development Diğer (Uluslararası) · Tamamlandı 2012-12-24 – 2014-01-10
  3. 2017 Role of Wnt signaling in the etiology of Filippi syndrome and ectrodactyly ectodermal dysplasia Diğer (Uluslararası) · Tamamlandı 2017-01-01 – 2019-12-31
  4. 2014 Molecular basis of disturbed neurogenesis in primary microcephaly Diğer (Uluslararası) · Tamamlandı 2014-01-01 – 2016-12-31
  5. 2021 Akut lenfoblastik lösemide MDM2 ve STAT3'ün Kombine Hedeflenmesinin Yeni Bir Tedavi Yaklaşımı Olarak Araştırılması -Tübitak 3501 · Tamamlandı 2021-12-01 – 2024-04-01

Books 2

  1. 2022 Describing genetic basis and disease pathogenesis of Filippi syndrome Cinius ISBN 978-625-6940-06-2 Bilimsel Kitap
  2. 2021 Identification of RBBP8 mutation in Pakistani families affected with Jawad Syndrome Cinius Yayınları ISBN 978-625-804-153-8 Bilimsel Kitap

Proceedings 11 See all (11) →

  1. 2017 Identification of Founder Mutation in Pakistani Families Affected With Jawad Syndrome 5th International Congress of the Molecular Biology Association of Turkey
  2. 2017 Identification of Founder Mutation in Pakistani Families Affected with Jawad Syndrome 14th Horizons in Molecular Biology and 11th Career Fair
  3. 2015 Filippi syndrome is aheterogenic disorder with a high proportion of CKAP2L mutations 31st Ernst Klenk Symposium in Molecular Medicine
  4. 2019 Pathogenic consequences of impaired Wnt signaling and DNA damage response delineates Filippi syndrome 35th Ernst Klenk Symposium in Molecular Medicine
  5. 2017 Identification of a founder mutation in Pakistani families affected with Jawad syndrome Arbeitsgemeinschaft Für Gen-Diagnostik e.V.

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Collaboration network

From the author lists of YÖKSİS publication records. Duplicate records of a work count once; institutions are co-authors’ current YÖKSİS affiliations.

Co-authors
75
With an akaturk profile
3
Turkish institutions
2
Co-authored works
%70

Academic co-authors 3

  1. ERHAN APTULLAHOĞLU Doçent · Bilecik Şeyh Edebali Üniversitesi same university 1
  2. GÖKHAN YİĞİT Öğretim Görevlisi (ders Vermekle Görevli) · Siirt Üniversitesi 1
  3. İLKNUR SUR ERDEM Doçent · Erciyes Üniversitesi 1

National collaboration 2 institutions

Within own university1 joint works · Bilecik Şeyh Edebali Üniversitesi

  1. Erciyes Üniversitesi 1 works · 1 academics
  2. Siirt Üniversitesi 1 works · 1 academics

Other co-authors (incl. international) 72

Italian Undiagnosed Diseases Network 1

Peter Nürnberg 6Muhammad Sajid Hussain 5Angelika Noegel 4Birgit Budde 3Holger Thiele 3Janine Altmüller 3Maria Asif 3Sigrid Tinschert 3Stefan Höning 3Uzma Abdullah 3Ehtisham Ul Haq Makhdoom 2Maria Iqbal 2Muhammad Jameel 2Muhammad Tariq 2Shahid Mahmood Baig 2ARWA ISHAQ KHAYYATAgatino BattagliaAmbrin FatimaAngelika Anna NoegelAnna C.E. HurstAnna NickelsenAyaz KhanBernd WollnikBirgit Susanne BuddeChiara De LucaChristian BeckerChristian NienbergDaana DaanaDirk LindenblattF. BrancatiGhulam HussainHagar MorShakedHammad YousafHaseeb AnwarIdan SegalIlyas AhmedIram AnjumJ. JoseJamshaid Mahmood BaigJennifer Hochscherf

Show all (72)

Juliann M. SavattK. NiefindKnut BrockmannLiza DouievLudwig EichingerLynn PaisMarwan ShinawiMohammad Reza ToliatMuhammad Jawad HassanMuhammad Mohsin Ali KhanMuhammad SherNadra Nasser SamraNatasha L. RudyNaveed Altaf MalikNicole FleischerPaola FortugnoPeter BurfeindPeter KrawitzPrerana WagleSaadia Maryam SaadiSajida RasoolSarah FischerSheffer ShefferSheraz KhanSilke KaulfussSusan M. WhiteSusanne MotamenySyeda Seema WaseemTzung-Chien HsiehWolfgang HöhneYun LiZafar Ali

Authors without an akaturk profile (international researchers, retired or former academics, students, clinicians) are grouped by name spelling; short forms such as “Gulluce M.” join the single full name they match.