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Employment (2)

Kayseri City Hospital: Kayseri, Kayseri, TR

2022-09-01 to present | Dr. (Medical Genetics)
Employment
Source: Self-asserted source
Muhammet Ensar Doğan

Erciyes Üniversitesi Tıp Fakültesi: Kayseri, Kayseri, TR

2019-03-11 to 2022-09-01 | Assistant Professor (Medical Genetics)
Employment
Source: Self-asserted source
Muhammet Ensar Doğan

Works (16)

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

British journal of haematology
2024-05-29 | Journal article
Contributors: veysel gök; Leblebisatan G; Dilek Gurlek Gokcebay; Güler S; Doğan ME; Tuğ Bozdoğan S; Ayça Koca Yozgat; Özcan A; Pekpak Şahinoğlu E; Tokgöz H et al.
Source: Self-asserted source
Muhammet Ensar Doğan

A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman–Diamond syndrome

British Journal of Haematology
2022 | Journal article
EID:

2-s2.0-85126357135

Part of ISSN: 13652141 00071048
Contributors: Alsavaf, M.B.; Verboon, J.M.; Dogan, M.E.; Azizoglu, Z.B.; Okus, F.Z.; Ozcan, A.; Dundar, M.; Eken, A.; Donmez-Altuntas, H.; Sankaran, V.G. et al.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier

EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities.

Journal of molecular medicine (Berlin, Germany)
2022-12-17 | Journal article | Author
Contributors: Heydari Z; Peshkova M; ZEYNEP BURCIN GONEN; Coretchi I; Eken A; Yay AH; Muhammet Ensar Doğan; Nuriye Gokce; Akalin H; Kosheleva N et al.
Source: Self-asserted source
Muhammet Ensar Doğan

Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey.

Breast (Edinburgh, Scotland)
2022-06-21 | Journal article
Source: Self-asserted source
Muhammet Ensar Doğan

A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia.

Clinica chimica acta; international journal of clinical chemistry
2022-02-12 | Journal article
Source: Self-asserted source
Muhammet Ensar Doğan

Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea

Journal of Neurogenetics
2021 | Journal article
EID:

2-s2.0-85103896043

Part of ISSN: 15635260 01677063
Contributors: Cerrah Gunes, M.; Gunes, M.S.; Vural, A.; Aybuga, F.; Bayram, A.; Bayram, K.K.; Sahin, M.I.; Dogan, M.E.; Ozdemir, S.Y.; Ozkul, Y.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier
grade
Preferred source (of 2)‎

The Effect of Gene Mutations on Metastasis and Overall Survival in Metastatic and Nonmetastatic Colon Cancers

Asian Pacific Journal of Cancer Prevention
2021 | Journal article
EID:

2-s2.0-85122581387

Part of ISSN: 2476762X 15137368
Contributors: Ozdemir, Y.; Cag, M.; Colak, E.; Coskun, N.; Başgöz, N.; Sarici, H.; Kaan, D.; Dogan, M.; Deniz, K.; İnanc, M. et al.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier

Varied phenotypic spectrum presenting of paroxysmal exercise–induced dyskinesia: a Turkish family with SLC2A1 mutation

Neurological Sciences
2021 | Journal article
EID:

2-s2.0-85110829319

Part of ISSN: 15903478 15901874
Contributors: Gultekin, M.; Dogan, M.E.; Simsir, G.; Basak, A.N.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions.

Pediatric nephrology (Berlin, Germany)
2021-06-29 | Journal article
Source: Self-asserted source
Muhammet Ensar Doğan

A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers.

Pediatric nephrology (Berlin, Germany)
2020-12-01 | Journal article
Source: Self-asserted source
Muhammet Ensar Doğan
grade
Preferred source (of 2)‎

Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant

Journal of Pediatric Hematology/Oncology
2020-03 | Journal article
Part of ISSN: 1077-4114
Source: Self-asserted source
Muhammet Ensar Doğan
grade
Preferred source (of 2)‎

Effects of thymoquinone in prevention of experimental contrastinduced nephropathy in rats

Iranian Journal of Basic Medical Sciences
2019 | Journal article
EID:

2-s2.0-85079758812

Part of ISSN: 20083874 20083866
Contributors: Topaloǧlu, U.S.; Sipahioǧlu, M.H.; Güntürk, I.; Akgün, H.; Doǧan, M.E.; Sönmez, G.; Elmali, F.; Yazici, C.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier

The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population

Molecular Biology Reports
2019-08 | Journal article
Part of ISSN: 0301-4851
Part of ISSN: 1573-4978
Source: Self-asserted source
Muhammet Ensar Doğan
grade
Preferred source (of 2)‎

Comorbidity of the congenital absence of the vas deferens

Andrologia
2018 | Journal article
EID:

2-s2.0-85042507397

Contributors: Akinsal, E.C.; Baydilli, N.; Dogan, M.E.; Ekmekcioglu, O.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier

Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder

Molecular Biology Reports
2018 | Journal article
EID:

2-s2.0-85047145197

Contributors: Balta, B.; Gumus, H.; Bayramov, R.; Korkmaz Bayramov, K.; Erdogan, M.; Oztop, D.B.; Dogan, M.E.; Taheri, S.; Dundar, M.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier

Prenatal diagnosis of upper extremity malformations with ultrasonography: Diagnostic features and perinatal outcome

Journal of Clinical Ultrasound
2017 | Journal article
EID:

2-s2.0-85005808078

Contributors: Kutuk, M.S.; Altun, O.; Tutus, S.; Dogan, M.E.; Ozgun, M.T.; Dundar, M.
Source: Self-asserted source
Muhammet Ensar Doğan via Scopus - Elsevier