Mehmet Seven

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 10

Top Venues

American journal of men's health

Immunological investigations

Global medical genetics

Ophthalmic genetics

Istanbul University-Cerrahpaşa

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Istanbul University-Cerrahpaşa Jan 01 1977

Turkey

Prof.Dr. :: Faculty of Medicine/Medical Genetics

Publications

Aysel Kalayci Yigin, Mustafa Tarık Alay, Serdal Uğurlu, Mehmet Seven
The First Case Report of 47,XXY/46,XX/46,XY Mosaic Klinefelter Syndrome Patient With Mixed Connective Tissue Disorder. American journal of men's health 17 (3) (2023)
Aysel Kalayci Yigin, Mustafa Tarık Alay, Serdal Uğurlu, Mehmet Seven
The First Case Report of 47,XXY/46,XX/46,XY Mosaic Klinefelter Syndrome Patient With Mixed Connective Tissue Disorder. American journal of men's health 17 (3) (2023)
Aysel Kalayci Yigin, Mustafa Tarık Alay, Serdal Uğurlu, Mehmet Seven
The First Case Report of 47,XXY/46,XX/46,XY Mosaic Klinefelter Syndrome Patient With Mixed Connective Tissue Disorder. American journal of men's health 17 (3) (2023)
Mehmet Seven, Aysel Kalayci Yigin, Deniz Agirbasli, Mustafa Tarik Alay, Faruk Kirbiyik, Mustafa Demir
Radiation exposure in pregnancy: outcomes, perceptions and teratological counseling in Turkish women. Annals of Saudi medicine 42 (3) (2022)
Aysel Kalaycı Yiğin, Senol Turan, Mustafa Tarık Alay, Yasin Kavla, Öznur Demirel, Mehmet Seven
Should chromosomal analysis be performed routinely during the baseline evaluation of the gender affirmation process? The outcomes of a large cohort of gender dysphoric individuals. International journal of impotence research (2022)
Bilge Batu Oto, Deniz Agirbasli, Oğuzhan Kılıçarslan, Gokhan Celik, Aysel Kalaycı Yiğin, Mehmet Seven, Huseyin Yetik
Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene. Ophthalmic genetics (2022)
Kubra Cigdem Pekkoc-Uyanik, Aysel Kalayci Yigin, Burak Dogangun, Mehmet Seven
Evaluation of IL1B rs1143634 and IL6 rs1800796 Polymorphisms with Autism Spectrum Disorder in the Turkish Children. Immunological investigations (2021)
Aysel Kalaycı Yiğin, Mehmet Bugrahan Duz, Mehmet Seven
Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation. Global medical genetics 9 (1) (2021)
Burcin Erkal, Aysel Kalayci Yigin, Sukru Palanduz, Selcuk Dasdemir, Mehmet Seven
The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome. American journal of men's health 12 (6) (2019)
Mehmet Bugrahan Duz, Selcuk Dasdemir, Aysel Kalayci Yigin, Mehmet Ali Akalin, Mehmet Seven
Three novel mutations in 20 patients with hereditary spastic paraparesis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 39 (9) (2018)

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Publication Activity (10 Years)

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Mehmet Seven