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akaturk Academic measurement
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Academician

FATMA MÜJGAN SÖNMEZ

Profesör

Yüksek İhtisas Üniversitesi Tıp Fakültesi Dahili Tıp Bilimleri Bölümü

Research topics OpenAlex
  1. Ana Dal Sağlık Bilimleri Temel Alanı
  2. Yan Dal Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)
Articles 123 YÖKSİS 123 · OpenAlex 0 Total citations 1,650 h-index 18 · OpenAlex Q1 articles 10 Scopus · WoS Q1 8 Best field rank #4,384 / 39,749 Main field · top 11.0% Co-authors 249 1 Turkish institutions

Citation impact

OpenAlex YÖKSİS articles matched in OpenAlex: 22 + YÖKSİS · co-author record: 22
h-index 18 Percentile in Türkiye: 89 #16 of 199 at their university by h-index
i10-index
29
Total citations
1,650
Top 3.9% in Türkiye
Per article
37.5
FWCI
2.57
1.00 = world average
World top 1%
2
World top 10%
13

Most cited articles

  1. Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder 2016 world top 1% 375 citations
  2. Exome sequencing can improve diagnosis and alter patient management 2012 world top 1% 261 citations
  3. The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome 2019 world top 10% 138 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. 22 articles (509 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: 5.

Field ranking

YÖKSİS ?

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
249
With an akaturk profile
1
Turkish institutions
1
Co-authored works
%83

Academic co-authors 1

  1. SİBEL KUL Profesör · Karadeniz Teknik Üniversitesi 5

National collaboration 1 institutions

  1. Karadeniz Teknik Üniversitesi 5 works · 1 academics

Other co-authors (incl. international) 248

Aynacı FM 42Sonmez FM 33Aynacı M 19Erduran E 17Mocan H 16Celep Figen 13Gedik Y 13Ökten A 13Aslan Y 12Aynacı O 9Odemis E 9Ahmetoğlu A 8Orhan F 8Aksoy A 7Karaguzel A 7Soylu H 6Topcu M 6Anlar B 5Baki A 5Cakir M 5Karagüzel G 5Bahadır S 4Kalyoncu M 4Sari A 4Sen Y 4Topaloglu H 4Turanlı G 4Aysun S 3Boz C 3Cizmeci MN 3Demir E 3Dilber E 3Erdol H 3Erpolat S 3Herguner O 3Kose G 3Kosehan D 3Saatci I 3Yalnızoglu D 3köksal İ 3

Show all (248)

Akelma AZ 2Akizu Naiara 2Aliyazicioglu R 2Altunbasak S 2Aydın OF 2Ayvaz A 2Cakir E 2Can G 2Cobanoglu U 2Deger O 2Donmez A 2Elmas R 2Fazlioglu K. 2Genc D 2Gleeson JG 2Guven A 2Isık Y 2Kanburoglu MK 2Kandil ST 2Mungan I 2Ozkara HA. 2Ozkaya A.K. 2Sarpkaya AÖ 2Schroth Jana 2Serin HM 2Topbas M 2Yayli S 2Yildirmis S 2Yıldız M 2Zaman D. 2Abdel-Hadi SAbdel-Salam GHAcar HAkalan NAkkol NAkyazici RAl-Baradie RaidahAl-Saana NAAlioglu ZAlpay K.Alver AApaydın TArslan Y.Aslan AAydemir VAydın HIAydın KAzam MBafna VBahat EBaki CBalcı YIBaudis MBauer PBaykal SBen-Omran TBenedicenti FBertan VBielas SBornemann ABozkaya H.Cai NaCakir F.Can ECansu ACantagrel VincentCay ACay PCeltikci BCimsit GClaeys KGCollazo ADixon-Salazar TJDogs EDufke AEkmen ÜErdeli SErsoz SFaqeih Eissa A.Fenstermaker AGFenstermaker Ali G.Finkel RSGabriel SBGabriel StaceyGarimella KVGleeson Joseph G.Goebel HHGoker ZGultop KGündüz SHarova GHesapcioglu SHill KJHocaoğlu ÇHolmes Edward W.Hosver IHäussler MImamoglu HIInzana FIsik BKabakus NKapicioglu ZKaraarslan GKaracal UNKarakas TKardeş BKarli Oguz KKingston HKirschner JKose OKosucu PKrieger MKutukoglu IKuzeyli KLia Taratuto AMansour LAMarzouki NMcCloskey DouglasMedne LMorisaki HirokoMorisaki TakayukiMuschke PNaviaux Robert K.Nickerson ElizabethNovarino GOkur HOlvera JOnder EOraby AzzaOren AOrun EOzdemir GeyikOzgun SPeksoylu BPirra LPolat ARenda YRivier FRoos ARosti Rasim OzgurRudnik-Schöneborn SRuss CSaleh Mohammed A.M.Sarı A. DoğuSchaffer AEScheliga Judith S.Scott EricSelim LSenbil NSenderek J.Serdaroglu ASilhavy JLSilhavy Jennifer L.Sinici ISivri SSonmez FM. Aksoy ASougnez CSpencer EmilySpengler SStanzial FStendel CSynofzik MTan HTas TTatli MMTay SKTekerekoglu BTolun A.Tosun IToyama KeikoTurgutalp HUcar FUdpa NUgur SBUsubutun AUsul HUyanik GUyguner OUzumcu AUçar BVan Vleet JeremyVaux KeithWand DWeis JWilliams DYaris NYavuzyilmaz AYayla SYazıcı AYigit AYilmaz AEYuksel CN.Yurtyapan O YYöntem TYıldıran AYıldız KZaki MSZaki Maha S.Zerres Kde Goede Cyıldırım RÇalışkan AÖmeroğlu AÖnder ÇÖrem AÖzdemir MÖzdirim EŞener M

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.

Indexes and citation percentiles

?
TR Index 1 articles
OpenAlex citation percentile
Top 1%2
Top 10%8
Avg · n 21 %79.1
Other counts

Scopus (SJR)

  • YÖKSİS rows 22

WoS (JCR)

  • YÖKSİS rows 22

Articles

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

123articles

Journals with publications

18 journals

Narrow down

Scopus (SJR)
Q110 Q27 Q34 Q41
WoS (JCR)
Q18 Q24 Q35 Q45
TR Index
1articles

Article list

  1. 2024 Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study The Cerebellum DOI 10.1007/s12311-024-01690-1 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 96.2%
  2. 2023 Recurrence of ARID1B-related Coffin-Siris Syndrome by possible gonadal mosaicism Clinical Dysmorphology DOI 10.1097/MCD.0000000000000473 YÖKSİS SJR Q3 JCR Q4 OpenAlex 41.2%
  3. 2023 TRAPPC9-Related Intellectual Disability: Report of Two New Cases and Review of the Literature Molecular Syndromology DOI 10.1159/000531439 YÖKSİS SJR Q4 JCR Q4 OpenAlex 83.5%
  4. 2023 Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly European Journal of Human Genetics DOI 10.1038/s41431-023-01461-2 YÖKSİS SJR Q1 JCR Q2 OpenAlex 89.6%
  5. 2022 Effects of treatment with clinically relevant valproate, carbamazepine, oxcarbazepine, topiramate, lamotrigine and levetiracetam on ovarian folliculogenesis in young rats Epilepsy Research DOI 10.1016/j.eplepsyres.2022.106966 YÖKSİS SJR Q2 JCR Q3 OpenAlex 80.2%
  6. 2021 SLC35A2-CDG: novel variants with two ends of the spectrum Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2021-0292 YÖKSİS SJR Q2 JCR Q4 OpenAlex 5.0%
  7. 2021 Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia European Journal of Human Genetics DOI 10.1038/s41431-021-00832-x YÖKSİS SJR Q1 JCR Q1 OpenAlex 89.1%
  8. 2020 Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation Brain and Development DOI 10.1016/j.braindev.2020.02.001 YÖKSİS SJR Q2 JCR Q3 OpenAlex 63.2%
  9. 2020 MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia Nature Communications DOI 10.1038/s41467-020-19919-y YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 92.0%
  10. 2019 Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans The American Journal of Human Genetics DOI 10.1016/j.ajhg.2019.02.018 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 90.4%
  11. 2019 Pediatric headache and neuroimaging: experience of two tertiary centers Child's Nervous System DOI 10.1007/s00381-019-04411-w YÖKSİS SJR Q2 JCR Q3 OpenAlex 73.9%
  12. 2019 Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome Genetics in Medicine DOI 10.1038/s41436-018-0368-y YÖKSİS SJR Q1 JCR Q1
  13. 2019 A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism The Turkish Journal of Pediatrics DOI 10.24953/turkjped.2019.01.014 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 60.3%
  14. 2018 Vitamin D status in children with headache: A case-control study Clinical Nutrition ESPEN DOI 10.1016/j.clnesp.2017.09.010 YÖKSİS SJR Q3 JCR Q3 OpenAlex 82.4%
  15. 2017 Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsy Intractable & Rare Diseases Research DOI 10.5582/irdr.2016.01075 YÖKSİS SJR Q2 JCR Q2 OpenAlex 82.9%
  16. 2017 Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database European Journal of Paediatric Neurology DOI 10.1016/j.ejpn.2017.06.004 YÖKSİS SJR Q1 JCR Q2 OpenAlex 75.0%
  17. 2016 Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder Cell DOI 10.1016/j.cell.2016.11.013 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.6%
  18. 2016 Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the <i>ARID1B</i> gene Intractable & Rare Diseases Research DOI 10.5582/irdr.2014.01040 YÖKSİS SJR Q2 JCR Q2 OpenAlex 74.6%
  19. 2015 Vitamin D Deficiency in Children With Newly Diagnosed Idiopathic Epilepsy Journal of Child Neurology DOI 10.1177/0883073814566627 YÖKSİS SJR Q2 JCR Q3 OpenAlex top 10% OpenAlex 96.8%
  20. 2014 Orbital and Multiple brain abscesses secondary to pseudomonas aeruginosa sepsis in a neonate Int Pediatrics YÖKSİS

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