Prof. Dr. MEHMET SEVEN

Yayın Ağı

Makaleler 76

1. Interaction between secondhand smoke exposure and IL-17 gene polymorphism in pediatric asthma

Oztosun B., Baskan A. K., Kalayci A., Ozceker D., SEVEN M., Cokugras H., et al.

JOURNAL OF ASTHMA , cilt.62, sa.11, ss.1950-1959, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

2. HMGA2 associated ceRNA-HOTAIR pathway in breast cancer patients from clinicopathological perspective.

Ercoşkun P., AĞIRBAŞLI D., VELİDEDEOĞLU M., SEVEN M., Kalayci A.

Turkish journal of medical sciences , cilt.55, sa.3, ss.782-791, 2025 (SCI-Expanded, Scopus, TRDizin)

3. **Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome**

Dogan M., Terali K., ERÖZ R., Kilic H., Gezdirici A., Gonullu B.

MOLECULAR BIOLOGY REPORTS , cilt.51, sa.1, 2024 (SCI-Expanded, Scopus)

4. A new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder

Kalaycı A., Ağırbaşlı D., Serdengecti N., Alay M. T., Tarakcioglu M. C., Seven M.

Psychiatric Genetics , cilt.34, sa.6, ss.134-139, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

5. A new perspective on isotretinoin in pregnancy: Pregnancy outcomes, evaluation of complex phenotypes, and importance of teratological counselling

Alay M. T., Kalayci A., Seven M.

European Journal of Obstetrics and Gynecology and Reproductive Biology , cilt.291, ss.148-155, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

6. 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

KALAYCI YİĞİN A., TURAN Ş., ALAY M. T., KAVLA Y., DEMİREL Ö., SEVEN M.

INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH , cilt.35, sa.5, ss.472-477, 2023 (SCI-Expanded, Scopus)

7. The First Case Report of 47,XXY/46,XX/46,XY Mosaic Klinefelter Syndrome Patient With Mixed Connective Tissue Disorder

KALAYCI YİĞİN A., Alay M. T., UĞURLU S., SEVEN M.

American Journal of Men's Health , cilt.17, sa.3, 2023 (SSCI, Scopus)

8. **Evaluation of the Effect of Delivery Mode on Methylation Changes in the Global DNA and the PTEN Gene**

YUVACI H. U., KALAYCI YİĞİN A., ASLAN M. M., ÖZDEMİR F., ÖZEL A., CEVRİOĞLU A. S., et al.

JOURNAL OF CLINICAL OBSTETRICS AND GYNECOLOGY , cilt.33, sa.2, ss.111-117, 2023 (ESCI, Scopus, TRDizin)

9. Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene

BATU OTO B., AĞIRBAŞLI D., KILIÇARSLAN O., Celik G., KALAYCI YİĞİN A., SEVEN M., et al.

OPHTHALMIC GENETICS , cilt.44, sa.1, ss.70-73, 2023 (SCI-Expanded, Scopus)

10. Frequency of Y chromosome Microdeletions in Turkish Infertile Men: Single Center Experience

agirbasli d., Erdogan G., Seven M., Kalayci Yigin A.

Genel Tıp Dergisi , cilt.32, sa.6, ss.737-739, 2022 (TRDizin)

11. Determination of cytokine profile and associated genes of the signaling pathway in HNSCC.

Kalayci Yigin A., Azzawri A., Ozturk K., Cora T., Seven M.

Journal of receptor and signal transduction research , cilt.42, sa.5, ss.462-468, 2022 (SCI-Expanded, Scopus)

12. Evaluation of IL1B rs1143634 and IL6 rs1800796 Polymorphisms with Autism Spectrum Disorder in the Turkish Children

Pekkoc Uyanik K. C., Kalayci Yigin A., Dogangun B., Seven M.

IMMUNOLOGICAL INVESTIGATIONS , cilt.51, sa.4, ss.766-777, 2022 (SCI-Expanded, Scopus)

13. Frequency of Y chromosome microdeletions in Turkish infertile men: Single Center Experience

KalayciYigin A., Erdogan G., AĞIRBAŞLI D., SEVEN M.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.88, 2022 (SCI-Expanded, Scopus)

14. 47,XXY/46,XX/46,XY mosaic Klinefelter Syndrome accompanied by mixed connective tissue disorder: A very rare case

KALAYCI YİĞİN A., ALAY M. T., AĞIRBAŞLI D., SEVEN M.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.30, sa.SUPPL 1, ss.448-449, 2022 (SCI-Expanded, Scopus)

15. Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation

KALAYCI YİĞİN A., Duz M. B., SEVEN M.

GLOBAL MEDICAL GENETICS , cilt.09, sa.01, ss.23-28, 2022 (ESCI)

16. Co-existing bipolar disease and 17q12 deletion: a rare case report

Bulu E., Kalayci Yigin A., Agirbasli D., Demirel Ö. F., Aksoy Poyraz C., Seven M.

PSYCHIATRIC GENETICS , cilt.32, sa.1, ss.30-33, 2022 (SCI-Expanded, Scopus)

17. The effect of medicarpin on PTEN/AKT signal pathway in head and neck squamous cell carcinoma.

Yiğin A. K., Donmez H., Hitit M., Seven S., Eser N., Kurar E., et al.

Journal of cancer research and therapeutics , cilt.18, sa.1, ss.180-184, 2022 (SCI-Expanded, Scopus)

18. A rare case of an NLRP12-associated autoinflammatory disease

Ayla A. Y., Eren H., Zare J., Calhan S. S., KARACAN İ., Seven M., et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.64, sa.4, 2021 (SCI-Expanded, Scopus)

19. Fetal Outcomes of Anti-epileptic Drug Use in Pregnancy: Teratologic Approach

KALAYCI YİĞİN A., ALAY M. T., SEVEN M.

TURKISH JOURNAL OF NEUROLOGY , cilt.27, sa.1, ss.27-33, 2021 (ESCI, Scopus, TRDizin)

20. Assessment of Fetal Rhesus D and Gender with Cell-Free DNA and Exosomes from Maternal Blood

Yasa B., Sahin O., Ocut E., SEVEN M., Sozer S.

REPRODUCTIVE SCIENCES , cilt.28, sa.2, ss.562-569, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

21. Evaluation of clinical and laboratory findings of patients with klinefelter syndrome: Single center experience Klinefelter sendromlu hastaların klinik ve laboratuvar bulgularının değerlendirilmesi: Tek merkez deneyimi

KALAYCI A., SEVEN M.

Turkiye Klinikleri Journal of Medical Sciences , cilt.41, sa.1, ss.63-69, 2021 (Scopus, TRDizin)

22. Konjenital Adrenal Hiperplazi Vakalarında CYP21A2 Geni Kopya Sayısı Değişimlerinin MLPA Tekniği İle İncelenmesi

MAMMADOV B., YİĞİN A. K., ÖZDEMİR F., ÖZAYDIN A., SEVEN M.

Phoenix Medical Journal , cilt.2, sa.1, ss.1-10, 2020 (Hakemli Dergi)

23. Investigation of methylation alterations on srd5a2 gene in patients with 5 alpha reductase type 2 enzyme deficiency 5 alfa redüktaz tip 2 enzim eksikliği olan hastalarda srd5a2 geni metilasyon değişikliklerinin araştırılması

Kirat E., KALAYCI YİĞİN A., Özdemir F., SEVEN M.

Turkiye Klinikleri Journal of Medical Sciences , cilt.40, sa.1, ss.68-73, 2020 (SCI-Expanded, Scopus, TRDizin)

24. Nadir ve Atipik Bulgularla Seyreden Bir Smith-Magenis Sendromu Vakası

Alay M. T., Kalaycı Yiğin A., Seven M.

Anka Tıp Dergisi , cilt.1, sa.1, ss.46-49, 2019 (Hakemli Dergi)

25. The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome

ERKAL B., Yigin A. K., Palanduz S., Dasdemir S., Seven M.

AMERICAN JOURNAL OF MENS HEALTH , cilt.12, sa.6, ss.2152-2156, 2018 (SSCI, Scopus)

26. Calculation of Embryo/Fetus Dose in Pregnant Thyroid Patients Who Have Accidentally Received Radioiodine

DEMİR M., ÇAVDAR İ., YEYİN N., Abuqubetah M., USLU BEŞLİ R. L., İpek N., et al.

Okmeydanı Tıp Dergisi , cilt.1, ss.1-4, 2018 (SCI-Expanded, Scopus, TRDizin)

27. Three novel mutations in 20 patients with hereditary spastic paraparesis.

Duz M. B., Dasdemir S., Yigin A., Akalin M. A., Seven M.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology , cilt.39, sa.9, ss.1551-1557, 2018 (SCI-Expanded, Scopus)

28. WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome

WHITE J. J., Mazzeu J. F., COBAN-AKDEMIR Z., BAYRAM Y., BAHRAMBEIGI V., HOISCHEN A., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.102, sa.1, ss.27-43, 2018 (SCI-Expanded, Scopus)

29. Neonatal fractures as a presenting feature of LMOD3-associated congenital myopathy

ABBOTT M., JAIN M., PFERDEHIRT R., CHEN Y., TRAN A., Duz M. B., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.173, sa.10, ss.2789-2794, 2017 (SCI-Expanded, Scopus)

30. A novel case of autosomal dominant cutis laxa in a consanguineous family: report and literature review

Duz M. B., Kirat E., Coucke P. J., Koparir E., Gezdirici A., De Paepe A., et al.

CLINICAL DYSMORPHOLOGY , cilt.26, sa.3, ss.142-147, 2017 (SCI-Expanded, Scopus)

31. Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome

LEE B., Duz M. B., SAGONG B., Koparir A., LEE K., CHOI J. Y., et al.

GENE , cilt.576, sa.2, ss.776-781, 2016 (SCI-Expanded, Scopus)

32. DNA repair gene XPD Asp312Asn and XRCC4 G-1394T polymorphisms and the risk of autism spectrum disorder

Dasdemir S., Guven M., Pekkoc K. C., Ulucan H., Dogangun B., Kirtas E., et al.

Cellular and Molecular Biology , cilt.62, sa.3, ss.46-50, 2016 (SCI-Expanded, Scopus)

33. Teratolojik Danışmanın Önemi

DAŞDEMİR S., DAŞDEMİR S.

Türkiye Klinikleri , cilt.1, sa.1, ss.115-118, 2016 (Hakemli Dergi)

34. Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

Karaca E., Harel T., Pehlivan D., Jhangiani S. N., Gambin T., Akdemir Z. C., et al.

NEURON , cilt.88, sa.3, ss.499-513, 2015 (SCI-Expanded, Scopus)

35. Determining and Managing Fetal Radiation Dose from Diagnostic Radiology Procedures in Turkey

Ozbayrak M., Cavdar I., Seven M., Uslu L., Yeyin N., Tanyildizi H., et al.

KOREAN JOURNAL OF RADIOLOGY , cilt.16, sa.6, ss.1276-1282, 2015 (SCI-Expanded, Scopus)

36. Whole-exome sequencing revealed two novel mutations in Usher syndrome

Koparir A., Karatas O. F., ATAYOGLU A. T., YUKSEL B., SAGIROGLU M. S., Seven M., et al.

GENE , cilt.563, sa.2, ss.215-218, 2015 (SCI-Expanded, Scopus)

37. Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes

YUAN B., PEHLIVAN D., KARACA E., PATEL N., CHARNG W., GAMBIN T., et al.

JOURNAL OF CLINICAL INVESTIGATION , cilt.125, sa.2, ss.636-651, 2015 (SCI-Expanded, Scopus)

38. Is the novel SCKL3 at 14q23 the predominant Seckel locus?

SEVEN M.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.23, sa.1, ss.140, 2015 (SCI-Expanded, Scopus)

39. The role of miRNAs in cancer: from pathogenesis to therapeutic implications

Seven M., Karatas O. F., Duz M. B., Ozen M.

FUTURE ONCOLOGY , cilt.10, sa.6, ss.1027-1048, 2014 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

40. Human CLP1 Mutations Alter tRNA Biogenesis, Affecting Both Peripheral and Central Nervous System Function

KARACA E., WEITZER S., PEHLIVAN D., SHIRAISHI H., GOGAKOS T., HANADA T., et al.

CELL , cilt.157, sa.3, ss.636-650, 2014 (SCI-Expanded, Scopus)

41. The Effect of Genetic Polymorphisms of Cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on Drug-Resistant Epilepsy in Turkish Children

Seven M., Batar B., Unal S., Yesil G., Yuksel A., Guven M.

MOLECULAR DIAGNOSIS & THERAPY , cilt.18, sa.2, ss.229-236, 2014 (SCI-Expanded, Scopus)

42. The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children

Seven M., Batar B., Unal S., Yesil G., Yuksel A., Guven M.

MOLECULAR BIOLOGY REPORTS , cilt.41, sa.1, ss.331-336, 2014 (SCI-Expanded, Scopus)

43. A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve-Melchior-Clausen syndrome

Seven M., Koparir E., Gezdirici A., Aydin H., Skladny H., Fenercioglu E., et al.

CLINICAL DYSMORPHOLOGY , cilt.23, sa.1, ss.1-7, 2014 (SCI-Expanded, Scopus)

44. A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication

Seven M., Gezdirici A., Ulucan H., Karatas O. F., Yosunkaya E., Yuksel A., et al.

GENE , cilt.527, sa.2, ss.675-678, 2013 (SCI-Expanded, Scopus)

45. Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism

Koroglu C., Seven M., Tolun A.

JOURNAL OF MEDICAL GENETICS , cilt.50, sa.8, ss.515-520, 2013 (SCI-Expanded, Scopus)

46. Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndrome

Ulucan H., Koparir E., Koparir A., Karaca E., Emre R., Gezdirici A., et al.

CLINICAL DYSMORPHOLOGY , cilt.22, sa.2, ss.87-90, 2013 (SCI-Expanded, Scopus)

47. Deficiency of selenium and zinc as a causative factor for idiopathic intractable epilepsy

Seven M., Basaran S. Y., Cengiz M., Unal S., Yuksel A.

EPILEPSY RESEARCH , cilt.104, ss.35-39, 2013 (SCI-Expanded, Scopus)

48. A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia

Gezdirici A., YENİGÜN A., Koparir E., Yosunkaya E., Ulucan H., Seven M., et al.

CLINICAL DYSMORPHOLOGY , cilt.22, sa.1, ss.33-35, 2013 (SCI-Expanded, Scopus)

49. THE VERY RARE AGLOSSIA ADACTYLIA SYNDROME WITH A NOVEL FINDING OF MENTAL RETARDATION

Seven M., Yosunkaya E., Guven G., Yuksel A.

GENETIC COUNSELING , cilt.23, sa.1, ss.81-85, 2012 (SCI-Expanded, Scopus)

50. A NEW SYNDROME PRESENTING WITH DYSMORPHIC FACIES, OCULOCUTANEOUS ALBINISM, GLAUCOMA, CRYPTORCHIDISM AND MENTAL RETARDATION

Seven M., Yosunkaya E., Yılmaz Ş., Karaca E., Guven G., Yuksel A.

GENETIC COUNSELING , cilt.22, sa.1, ss.25-34, 2011 (SCI-Expanded, Scopus)

51. SUDDEN VISION LOSS IN A MUCOPOLYSACCHARIDOSIS I PATIENT RECEIVING ENZYME REPLACEMENT THERAPY

Yosunkaya E., Karaca E., Yılmaz Ş., Gezdirici A., Guven G., Seven M., et al.

GENETIC COUNSELING , cilt.22, sa.4, ss.371-376, 2011 (SCI-Expanded, Scopus)

52. Marked Improvement in Segawa Syndrome After L-Dopa and Selegiline Treatment

Yosunkaya E., Karaca E., Basaran S., Seven M., Yuksel A.

PEDIATRIC NEUROLOGY , cilt.42, sa.5, ss.348-350, 2010 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

53. Warburg Micro syndrome in a Turkish boy

Yueksel A., Yesil G., Aras C., Seven M.

CLINICAL DYSMORPHOLOGY , cilt.16, sa.2, ss.89-93, 2007 (SCI-Expanded, Scopus)

54. Facial dysmorphism in Leigh syndrome with SURF-1 mutation and COX deficiency

Yuksel A., Seven M., Cetincelik Ü., Yesil G., köksal v.

PEDIATRIC NEUROLOGY , cilt.34, sa.6, ss.486-489, 2006 (SCI-Expanded, Scopus)

55. Is the novel SCKL3 at 14q23 the predominant Seckel locus?

KILINC M., NINIS V., UGUR S., Tuysuz B., SEVEN M., BALCI S., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.11, sa.11, ss.851-857, 2003 (SCI-Expanded, Scopus)

56. Antioxidant system in Down syndrome: A possible role in cataractogenesis

Cengiz M., Seven M., Suyugul N.

GENETIC COUNSELING , cilt.13, sa.3, ss.339-342, 2002 (SCI-Expanded, Scopus)

57. Dysmorphic face in two siblings with infantile neuroaxonal dystrophy

Seven M., Ozkilic A. Ç., Yuksel A.

GENETIC COUNSELING , cilt.13, sa.4, ss.465-473, 2002 (SCI-Expanded, Scopus)

58. A case of acampomelic campomelic dysplasia

Ozkilic A. Ç., Seven M., Yuksel A.

GENETIC COUNSELING , cilt.13, sa.1, ss.23-28, 2002 (SCI-Expanded, Scopus)

59. Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation

Seven M., Karaman B., Hacihanefioglu S., Deviren A., Yuksel A., Basaran S.

CLINICAL DYSMORPHOLOGY , cilt.11, sa.1, ss.39-42, 2002 (SCI-Expanded, Scopus)

60. Plasma carnitine levels in children with Down Syndrome

Seven M., Cengiz M., Tuzgen S., Iscan M.

AMERICAN JOURNAL OF HUMAN BIOLOGY , cilt.13, sa.6, ss.721-725, 2001 (SCI-Expanded, SSCI, Scopus)

61. Changes in the antioxidant system in epileptic children receiving antiepileptic drugs: Two-year prospective studies

Yuksel A., Cengiz M., Seven M., Ulutin T.

JOURNAL OF CHILD NEUROLOGY , cilt.16, ss.603-606, 2001 (SCI-Expanded, Scopus)

62. A case of symbrachydactyly with oligodactyly

Seven M., Yuksel A., Ozkilic A. Ç.

GENETIC COUNSELING , cilt.12, sa.1, ss.77-83, 2001 (SCI-Expanded, Scopus)

63. Infantile-onset megalencephalic leucoencephalopathy in two siblings

Soylu H., Yuksel A., Kutlu N., Aydinli M., Seven M., Mocan H.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH , cilt.36, sa.6, ss.598-602, 2000 (SCI-Expanded, Scopus)

64. The effects of carbamazepine and valproic acid on the erythrocyte glutathione, glutathione peroxidase, superoxide dismutase and serum lipid peroxidation in epileptic children

Cengiz M., Yuksel A., Seven M.

PHARMACOLOGICAL RESEARCH , cilt.41, ss.423-425, 2000 (SCI-Expanded) Sürdürülebilir Kalkınma

65. . Erythrocyte Glutathione, Glutathione Peroxidase, Superoxide Dismutase and Serum Lipid Peroxidation in Epileptic Children With Valproate And Carbamazepine Monotherapy

Yüksel A., CENGİZ M., SEVEN M., ULUTİN T.

J Basic Clin Physiol Pharmacol , cilt.11, sa.1, ss.73-81, 2000 (Scopus)

66. Down Sendromlularda Glutatyon, Glutatyon Peroksidaz ve Glutatyon S Transferaz Düzeyleri

Seven M., Sılan F., Cengiz M., Hacıhanefioğlu S.

Acta Veterinaria-Beograd , cilt.1, sa.2, ss.40-44, 2000 (SCI-Expanded, Scopus, TRDizin)

67. Vitamin and mineral status in Down syndrome

CENGIZ M., SEVEN M., Cengiz S., YUKSEL A., ISCAN M.

TRACE ELEMENTS AND ELECTROLYTES , cilt.17, sa.3, ss.156-160, 2000 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

68. A variant of Cenani-Lenz type syndactyly

Seven M., Yuksel A., Ozkilic A. Ç., Elcioglu N.

GENETIC COUNSELING , cilt.11, sa.1, ss.41-47, 2000 (SCI-Expanded, Scopus)

69. Neuroimaging findings of four patients with Sandhoff disease

Yuksel A., Yalcinkaya C., Islak C., Gunduz E., Seven M.

PEDIATRIC NEUROLOGY , cilt.21, sa.2, ss.562-565, 1999 (SCI-Expanded, Scopus)

70. N-acetyl-beta-glucosaminidase and beta-galactosidase activity in children receiving antiepileptic drugs

Yuksel A., Cengiz M., Seven M., Cengiz S., Cenani A.

PEDIATRIC NEUROLOGY , cilt.20, ss.24-26, 1999 (SCI-Expanded, Scopus)

71. Two female siblings with a previously unreported MCA/MR syndrome: Pre and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles

Yuksel A., Seven M., Deviren A., Soylemez M., Hacihanefioglu S., Ulutin T., et al.

GENETIC COUNSELING , cilt.10, sa.3, ss.265-269, 1999 (SCI-Expanded, Scopus)

72. Mohr-Majewski syndrome (orofaciodigital syndrome type IV) in five sibs

Tuysuz B., ARAPOGLU M., SEVEN M., CENANI A.

GENETIC COUNSELING , cilt.10, sa.2, ss.189-192, 1999 (SCI-Expanded, Scopus)

73. A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations

Seven M., Suyugul Z., Yuksel A., Geckinli B., Hacihanefioglu S., Cenani A.

TURKISH JOURNAL OF PEDIATRICS , cilt.40, sa.4, ss.593-601, 1998 (SCI-Expanded, Scopus, TRDizin)

74. Hipertrofik Kardiyomiyopati ailelerinde 403 Arg-Gln Missens nokta mutasyonu ve bunun ani kardiyak ölümle ilişkisi

SEVEN M., Küçükateş E., Ersanlı M., Gültekin N., Sayhan N.

TÜRK KARDİYOLOJİ DERNEĞİ ARŞİVİ , cilt.11, sa.27, ss.664-671, 1997 (Scopus)

75. b-Galactosidase and b-Glicosidase Enzyme Levels in healthy Turkish Children

SEVEN M., Yüksel A., Cengiz M., Elçioğlu n., Cenani A.

Türk Biyokimya Dergisi , cilt.22, sa.2, ss.21-24, 1996 (Hakemli Dergi)

76. otozomal Resesif Kolobomatöz Mikroftalmi

SEVEN M., Suyugül Z., Yüksel A., Cenani A.

MN OFTALMOLOJİ , cilt.1, sa.3, ss.99-102, 1996 (TRDizin)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 13

1. Evaluation of Clinical Findings and Molecular Genetic Results of the Patients with CACNA1A Variants: Single Center Experience

Ovunc S., KALAYCI A., GÜLER S., Cinar C., AĞIRBAŞLI D., Seven M.

75th Annual Meeting of the American-Academy-of-Neurology (AAN), Massachusetts, Amerika Birleşik Devletleri, 22 - 27 Nisan 2023, (Özet Bildiri)

2. Novel Variants and Phenotypic Heterogeneity in Congenital Insensitivity to Pain

Ovunc S., Yigin A. K., Kesriklioglu B., Izgi G., Ulug F., SALTIK S., et al.

75th Annual Meeting of the American-Academy-of-Neurology (AAN), Massachusetts, Amerika Birleşik Devletleri, 22 - 27 Nisan 2023, sa.17, (Özet Bildiri)

3. Effects of Environmental Factors on Human Health and Expert Suggestions

SEVEN M.

International Congress on, Saray Bosna, Bosna-Hersek, 31 Temmuz - 05 Ağustos 2017, ss.7-8, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

4. Why is the teratological counseling necessary?

SEVEN M., DEMİR M.

European Society of Human Genetics, Barcelona, İspanya, 21 - 24 Mayıs 2016, cilt.24, sa.1, ss.402, (Tam Metin Bildiri)

5. The role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in susceptibility to childhood acute lymphoblastic leukemia

GÜVEN M., Batar B., CELKAN T. T., Özdemir N., GÜVEN G., Yosunkaya E., et al.

Joint International Conferance of the African and Southern African Societies of Human Genetics, Cape Town, Güney Afrika, 6 - 09 Mart 2011, ss.111, (Tam Metin Bildiri)

6. Turner Sendromu tanısıyla başvuran hastalarda gözlenen sitogenetik bulgular.

YILMAZ Ş., TARKAN ARGÜDEN Y., KURU R. D., ÇIRAKOĞLU A., SAĞCI GÜVEN G., KURT H., et al.

X. Ulusal Tıbbi Biyoloji ve Genetik Kongresi,, Antalya, Türkiye, ss.226, (Tam Metin Bildiri)

7. Two cases with Williams syndrome

Kuru K., Cirakoglu A., Tarkan-Arguden Y., Yilmaz S., Guven G. S., Cinar A., et al.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.96-97, (Özet Bildiri)

8. Cytogenetic findings in Joubert syndrome

Fenerci Y., Karaca E., Kuru D., Cirakoglu A., Seven M., Deviren A., et al.

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