Araştırmacı AYLA ŞAHİN

Yayın Ağı

Makaleler 6

1. A Novel ADRA1A Missence Variant (c.939G > T) in Two Related Patients with Anejaculation: Case Report

Sharifi S., Dursun M., Palanduz S., Sahin A., Kadioglu A.

Indian Journal of Clinical Biochemistry , cilt.41, sa.1, ss.140-143, 2026 (ESCI, Scopus)

2. EVALUATION OF GENETIC TESTING IN ADULT PATIENTS WITH SUSPECTED SYSTEMIC AUTOINFLAMMATORY DISORDERS

Amikishiyev S., Engin Y. A., KALAYCI T., Soltanova L., YALÇINKAYA Y., ARTIM ESEN B., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , cilt.89, sa.1, ss.70-81, 2026 (ESCI, Scopus, TRDizin)

3. Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes

Sharifi S., DURSUN M., Sahin A., TURAN S., ALTUN A., Ozcan O., et al.

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , cilt.42, sa.4, ss.1223-1237, 2025 (SCI-Expanded, Scopus)

4. **Clinical Features of the Patients with NLRP1 Gene Variants and a Systemic Autoinflammatory Phenotype**

AMIKISHIYEV S., KALAYCI T., Deniz R., YALÇINKAYA Y., ARTIM ESEN B., İNANÇ M., et al.

ARTHRITIS & RHEUMATOLOGY , ss.3800-3802, 2023 (SCI-Expanded)

5. Phenotypes of the Patients with More Than One Autoinflammatory Gene Variant: Classified Diseases and Mixed Autoinflammatory Disorders (MAID)

Amıkıshıyev S., Kalaycı T., Soltanova L., Yalçınkaya Y., Artim-Esen B., İnanç M., et al.

ARTHRITIS & RHEUMATOLOGY , ss.506-508, 2023 (SCI-Expanded)

6. Is there a relationship between ACTN3 R577X gene polymorphism and sarcopenia?

Kahraman M., Ozulu Turkmen B., Bahat-Ozturk G., Catikkas N. M., Oren M. M., Sahin A., et al.

AGING CLINICAL AND EXPERIMENTAL RESEARCH , cilt.34, sa.4, ss.757-765, 2022 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 6

1. Genetic insights into non-obstructive azoospermia: Identifying novel variants and enhancing clinical outcomes

Sharifi S., Dursun M., Şahin A., Altun A., Turan S., Özcan Ö., et al.

40th Annual EAU Congress, Madrid, İspanya, 21 - 24 Mart 2025, ss.87, (Özet Bildiri)

2. Integrated Multi-Omics Approach for Investigating Molecular Insights into Non-Obstructive Azoospermia and Association with Potential Cancer Susceptibility

Sharifi S., Dursun M., Şahin A., Özcan Ö., Turan S., Kadıoğlu A., et al.

23. Ulusal Androloji Kongresi, Eskişehir, Türkiye, 17 - 19 Mayıs 2024, ss.22, (Özet Bildiri)

3. First Report Unveiling Genetic Etiopathogenesis of Anejaculation: Involvement of Alpha-1a Adrenergic Receptor Gene in a in Familial Cases

Sharifi S., Dursun M., Palanduz Ş., Şahin A., Kadıoğlu A.

23. Ulusal Androloji Kongresi, Eskişehir, Türkiye, 17 - 19 Mayıs 2024, ss.14, (Özet Bildiri)

4. Wilson Hastalığında Aile İçi Genetik Taramanın Kliniğe Önemli Katkıları

Şahin A., ÇİFCİBAŞI ÖRMECİ A., SUER İ., DEMİR K., KALAYCI T., ÇEFLE K., et al.

40. Ulusal Gastroenteroloji Haftası ve 11. Gastroenteroloji Cerrahisi Kongresi, Antalya, Türkiye, 21 - 26 Kasım 2023, (Özet Bildiri)

5. Herediter Periyodik Ateş Sendromu Düşünülen Hastalarda Ateş Paneli ile Yapılan Genetik İncelemelerin Sonuçları

AMİKİSHİYEV S., KALAYCI T., BEKTAŞ M., ÇETİN Ç., AGHAMURADOV S., YALÇIN DULUNDU B. Ç., et al.

XXII. ULUSAL ROMATOLOJİ KONGRESİ, Antalya, Türkiye, 26 - 30 Ekim 2022, ss.128-129, (Özet Bildiri)

6. Relationship between sarcopenia and ACTN3 R577X gene in older adults

Kahraman M., Özulu Türkmen B., Bahat-Öztürk G., Şahin A., Aday A., Diler A. S., et al.

16th International E-Congress of the European Geriatric Medicine Society, Lisbon, Portekiz, 7 - 09 Ekim 2020, ss.461, (Özet Bildiri)

Metrikler

Araştırmacı AYLA ŞAHİN

Yayınlar & Eserler

1. A Novel ADRA1A Missence Variant (c.939G > T) in Two Related Patients with Anejaculation: Case Report

2. EVALUATION OF GENETIC TESTING IN ADULT PATIENTS WITH SUSPECTED SYSTEMIC AUTOINFLAMMATORY DISORDERS

3. Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes

4. **Clinical Features of the Patients with NLRP1 Gene Variants and a Systemic Autoinflammatory Phenotype**

5. Phenotypes of the Patients with More Than One Autoinflammatory Gene Variant: Classified Diseases and Mixed Autoinflammatory Disorders (MAID)

6. Is there a relationship between ACTN3 R577X gene polymorphism and sarcopenia?

1. Genetic insights into non-obstructive azoospermia: Identifying novel variants and enhancing clinical outcomes

2. Integrated Multi-Omics Approach for Investigating Molecular Insights into Non-Obstructive Azoospermia and Association with Potential Cancer Susceptibility

3. First Report Unveiling Genetic Etiopathogenesis of Anejaculation: Involvement of Alpha-1a Adrenergic Receptor Gene in a in Familial Cases

4. Wilson Hastalığında Aile İçi Genetik Taramanın Kliniğe Önemli Katkıları

5. Herediter Periyodik Ateş Sendromu Düşünülen Hastalarda Ateş Paneli ile Yapılan Genetik İncelemelerin Sonuçları

6. Relationship between sarcopenia and ACTN3 R577X gene in older adults

Yayın

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Atıf (Scholar)

H-İndeks (Scholar)

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