Prof. Dr. Ali KARAMAN

1. Ultrasonographic evaluation of fetal posterior fossa anomalies: Six years experience of a tertiary center

Taşdemir Ü., EYİSOY Ö. G., KARAMAN A., Demirci O.

Journal of Clinical Ultrasound , cilt.53, sa.1, ss.24-32, 2025 (SCI-Expanded, Scopus)

2. Aberrant right subclavian artery in the absence of other prenatal ultrasound findings: Should we still be concerned?

Odacılar A. Ş., Ayhan I., KARAMAN A., Demirci O.

Journal of Clinical Ultrasound , cilt.52, sa.8, ss.1096-1102, 2024 (SCI-Expanded, Scopus)

3. Molecular analysis of 31 cases with fetal skeletal dysplasia

Taşdemir Ü., EYİSOY Ö. G., Gezer M., KARAMAN A., Demirci O.

Journal of Perinatal Medicine , cilt.52, sa.8, ss.886-895, 2024 (SCI-Expanded, Scopus)

4. Revisiting Atrioventricular Septal Defects: Exploring Chromosomal Abnormalities, Cardiac and Extracardiac Anomalies in a Contemporary Prenatal Cohort

Ayhan I., Demirci O., Odacılar A. Ş., YÜCEL İ. K., KARAMAN A.

Pediatric Cardiology , cilt.45, sa.5, ss.1036-1047, 2024 (SCI-Expanded, Scopus)

5. An analysis of factors affecting survival in prenatally diagnosed omphalocele

Ayhan I., Demirci O., Uygur L., Odacilar Ş., Özbay Ayvaz O. D., KARAMAN A., et al.

Journal of Perinatal Medicine , cilt.51, sa.9, ss.1189-1196, 2023 (SCI-Expanded, Scopus)

6. Contribution of chromosomal microarray analysis and next-generation sequencing to genetic diagnosis in fetuses with normal karyotype

AKALIN M., Demirci O., Dizdaroğulları G. E., Çiftçi E., KARAMAN A.

Journal of Obstetrics and Gynaecology Research , cilt.49, sa.2, ss.519-529, 2023 (SCI-Expanded, Scopus)

7. Foetal thoracic hypoplasia: concomitant anomalies and neonatal outcomes

Akalin M., Demirci O., Bolat G., Kahramanoglu O., ERİÇ ÖZDEMİR M., KARAMAN A.

Journal of Obstetrics and Gynaecology , cilt.42, sa.5, ss.848-853, 2022 (SCI-Expanded, Scopus)

8. Can FMR1 CGG repeat lengths predict the outcome in ICSI cycles?

Cogendez E., Ozkaya E., Eser A. Ç., Eken M., KARAMAN A.

Ginekologia Polska , cilt.93, sa.9, ss.735-741, 2022 (SCI-Expanded, Scopus)

9. Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg

Cetinkaya A., KARAMAN A., Mutlu M. B., Yavuz T.

Congenital Anomalies , cilt.58, sa.1, ss.41-43, 2018 (SCI-Expanded, Scopus)

10. A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus

Mutlu M. B., Cetinkaya A., KOÇ N., CEYLANER G., Erguner B., Aydın H., et al.

European Journal of Medical Genetics , cilt.59, sa.11, ss.604-606, 2016 (SCI-Expanded, Scopus)

11. Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort

Aydin H., GÜNAY M., Celik G., Gunay B. O., Aydin U. T., KARAMAN A.

Ophthalmic Genetics , cilt.37, sa.4, ss.415-418, 2016 (SCI-Expanded, Scopus)

12. Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin

Bayram Y., Karaca E., Akdemir Z. C., YILMAZ B. E., Tayfun G. A., Aydin H., et al.

Journal of Clinical Investigation , cilt.126, sa.2, ss.762-778, 2016 (SCI-Expanded, Scopus)

13. Evaluation of maternal serum folate, vitamin b12, and homocysteine levels and factor V leiden, factor II g.20210G>A, and MTHFR variations in prenatally diagnosed neural tube defects

Aydin H., Arisoy R., KARAMAN A., Erdoğdu E., Çetinkaya A., GEÇKİNLİ B. B., et al.

Turkish Journal of Medical Sciences , cilt.46, sa.2, ss.489-494, 2016 (SCI-Expanded, Scopus, TRDizin)

14. Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI

Bayram Y., Aydin H., Gambin T., Akdemir Z. C., Atik M. M., Karaca E., et al.

American Journal of Medical Genetics, Part A , cilt.167, sa.9, ss.2132-2137, 2015 (SCI-Expanded, Scopus)

15. DNA damage is increased in lymphocytes of patients with metabolic syndrome

KARAMAN A., Aydin H., Geçkinli B., Çetinkaya A., Karaman S.

Mutation Research - Genetic Toxicology and Environmental Mutagenesis , cilt.782, ss.30-35, 2015 (SCI-Expanded, Scopus)

16. Concomitant omphalocele, anencephaly and arthrogryposis associated with trisomy 18

KARAMAN A., Aydin H., Göksu K.

Genetic Counseling , cilt.26, sa.1, ss.77-79, 2015 (SCI-Expanded, Scopus)

17. Clinical report of a patient with de novo trisomy 12q23.1q24.33

GEÇKİNLİ B. B., Aydin H., KARAMAN A., Delil K., Simsek H., Gokmeydan E., et al.

Genetic Counseling , cilt.26, sa.4, ss.393-400, 2015 (SCI-Expanded, Scopus)

18. Agenesis of the ductus venosus a case with noonan syndrome

Demirci O., Yavuz T., Arisoy R., Pekin O., Acar H., Aydin H., et al.

Genetic Counseling , cilt.26, sa.3, ss.373-376, 2015 (SCI-Expanded, Scopus)

19. Co-occurrence of neural tube defect, thoracal defect and omphalocele: A rare case and review of the literature

Aydin H., Arisoy R., Simsek H., Erdogdu E., GEÇKİNLİ B. B., KARAMAN A., et al.

Genetic Counseling , cilt.26, sa.2, ss.253-257, 2015 (SCI-Expanded, Scopus)

20. A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH

GEÇKİNLİ B. B., Aydin H., KARAMAN A.

Genetic Counseling , cilt.25, sa.4, ss.405-412, 2015 (SCI-Expanded, Scopus)

21. The deletion 22q13 syndrome: A new case

KARAMAN A., Aydin H., Geçkinli B., Göksu K.

Genetic Counseling , cilt.26, sa.1, ss.53-60, 2015 (SCI-Expanded, Scopus)

22. Prevalence of X-aneuploidies, X-structural abnormalities and 46,XY sex reversal in Turkish women with primary amenorrhea or premature ovarian insufficiency

GEÇKİNLİ B. B., TOKSOY G., Sayar C., SÖYLEMEZ M. A., Yesil G., Aydin H., et al.

European Journal of Obstetrics and Gynecology and Reproductive Biology , cilt.182, ss.211-215, 2014 (SCI-Expanded, Scopus)

23. Craniorachischisis, gastroschisis, and a branchial sinus defect: A case report

Aydin H., Yanik S., TUĞ E., Ahsen H., Geckinli B., Senol S., et al.

Genetic Counseling , cilt.25, sa.2, ss.237-240, 2014 (SCI-Expanded, Scopus)

24. Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia

Pehlivan D., Karaca E., Aydin H., Beck C. R., Gambin T., Muzny D. M., et al.

European Journal of Human Genetics , cilt.22, sa.9, ss.1145-1148, 2014 (SCI-Expanded, Scopus)

25. A typical case with apert syndrome Apert sendromlu tipik bir olgu

Aydin H., Geçkinli B., KARAMAN A.

Goztepe Tip Dergisi , cilt.29, sa.2, ss.115-117, 2014 (Scopus, TRDizin)

26. Osteogenesis imperfecta associated with partial trisomy 20p: Case report Osteogenezis İmperfekta ile Parsiyel Trizomi 20p Birlikteliği: Olgu Sunumu

KARAMAN A., Tos T., Geçkİnlİ B., Aydin H.

Goztepe Tip Dergisi , cilt.29, sa.3, ss.192-195, 2014 (Scopus, TRDizin)

27. Relation of chronic atrophic gastritis and intestinal metaplasia with helicobacter pylori and tumor necrosis factor-α and macrophage migration inhibitory factor polymorphisms in a population of Easten Anatolia Türkiye’de bir doğu populasyonunda kronik atrofik gastrit ve intestinal metaplazi ile tümör nekrozis faktör-α ve makrofaj migrasyon inhibitör faktör gen polimorfizmleri ve Helikobakteri pilorinin ilişkisi

KARAMAN A., Aydin H., Geçkİnlİ B., BİNİCİ D. N., Pİrİm İ.

Goztepe Tip Dergisi , cilt.29, sa.1, ss.12-19, 2014 (Scopus, TRDizin)

28. Split-hand, and split-foot malformations: A family Yarık el/yarık ayak malformasyonlu bir aile

KARAMAN A., Tos T., Geçkİnlİ B., Aydin H., Ataoğlu S.

Goztepe Tip Dergisi , cilt.29, sa.1, ss.69-72, 2014 (Scopus, TRDizin)

29. Fraser syndrome: A new case Fraser sendromu: Yeni bir olgu

KARAMAN A., Geçkinli B., Aydin H.

Goztepe Tip Dergisi , cilt.29, sa.1, ss.60-61, 2014 (Scopus, TRDizin)

30. Tetrasomy 12p presenting with long appendix: A prenatal case

Aydin H., Arisoy R., Geckinli B., Erdogdu E., KARAMAN A., Gokmeydan E., et al.

Genetic Counseling , cilt.24, sa.4, ss.439-440, 2013 (SCI-Expanded, Scopus)

31. Genomic damage in patients with type-2 diabetes mellitus

BİNİCİ D. N., KARAMAN A., Coşkun M., Uyanik Oǧlu A., Uçar F.

Genetic Counseling , cilt.24, sa.2, ss.149-156, 2013 (SCI-Expanded, Scopus)

32. Duplication 10q syndrome: A new case

KARAMAN A., Tos T.

Goztepe Tip Dergisi , cilt.28, sa.1, ss.55-57, 2013 (Scopus, TRDizin)

33. Noonan syndrome: Case report Noonan sendromu: Olgu sunumu

KARAMAN A., KESKİN H., KAÇMAZ E., LALOĞLU F., Ömeroǧullari Z.

Goztepe Tip Dergisi , cilt.28, sa.1, ss.48-50, 2013 (Scopus, TRDizin)

34. Micronucleus analysis in behçet's disease with and without HLA-B51 HLA-B51 pozitif ve negatif behçet hastalıǧında mikronükleus analizi

BİNİCİ D. N., KARAMAN A., Kadi M.

Turkiye Fiziksel Tip ve Rehabilitasyon Dergisi , cilt.59, sa.1, ss.36-41, 2013 (SCI-Expanded, Scopus, TRDizin)

35. Apert syndrome: Case report Apert sendromu: Olgu sunumu

KARAMAN A., Kahveci H.

Medical Journal of Bakirkoy , cilt.9, sa.2, ss.81-84, 2013 (Scopus, TRDizin)

36. Goldenhar's syndrome: Case report Goldenhar sendromu: Olgu sunumu

KARAMAN A., LALOĞLU F., Kahveci H.

Medical Journal of Bakirkoy , cilt.9, sa.3, ss.131-133, 2013 (Scopus, TRDizin)

37. Jarcho-levin syndrome (spondylocostal dysostosis) and hydrocephalia: Case report

KARAMAN A., Kahveci H., LALOĞLU F.

Medical Journal of Bakirkoy , cilt.9, sa.4, ss.183-185, 2013 (Scopus, TRDizin)

38. Aplasia cutis congenita and limb anomaly: A case of non-scalp lesion Aplazia kutis kongenita ve ekstremite anomalisi: Non-skalp lezyonlu bir olgu

KARAMAN A., Kahvecİ H., KAÇMAZ E., Ataoğlu S.

Goztepe Tip Dergisi , cilt.28, sa.4, ss.220-223, 2013 (Scopus, TRDizin)

39. Phototherapy causes a transient DNA damage in jaundiced newborns

Kahveci H., DOĞAN H., KARAMAN A., Caner I., TAŞTEKİN A., Ikbal M.

Drug and Chemical Toxicology , cilt.36, sa.1, ss.88-92, 2013 (SCI-Expanded, Scopus)

40. Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: A new series of 24 patients

Tos T., KARAMAN A., Aksoy A., Tukun A.

Genetic Counseling , cilt.23, sa.2, ss.289-296, 2012 (SCI-Expanded, Scopus)

41. Genetic alterations in benign, preneoplastic and malignant breast lesions

KABALAR M. E., KARAMAN A., Aylu B., Erdem I., ÖZMEN S.

Indian Journal of Pathology and Microbiology , cilt.55, sa.3, ss.319-325, 2012 (SCI-Expanded, Scopus)

42. Roberts-SC phocomelia syndrome: Case report Roberts-SC fokomeli sendromu: Olgu sunumu

KARAMAN A., Kahveci H.

Haseki Tip Bulteni , cilt.50, sa.2, ss.66-68, 2012 (Scopus, TRDizin)

43. Trisomy 18 syndrome: Case report Trizomi 18 Sendromu: Olgu Sunumu

KARAMAN A., Kahveci H., LALOĞLU F.

Medical Journal of Bakirkoy , cilt.8, sa.1, ss.44-46, 2012 (Scopus, TRDizin)

44. A case with type maroteux of acromesomelic displasia Maroteaux tip-akromezomeli̇k di̇splazi̇li̇ bi̇r olgu

Tos T., KARAMAN A.

SENDROM , cilt.23, sa.4-6, ss.45-46, 2011 (Scopus)

45. Thanatophoric dyspalsia: Case report Tanatofori̇k di̇splazi̇

KARAMAN A., Kahveci H., ARSLAN R.

SENDROM , cilt.23, sa.4-6, ss.49-50, 2011 (Scopus)

46. Congenital contractural arachnodactyly (Beals-Hecht syndrome): A case report Konjenital kontraktural araknodaktili (Beals-Hecht sendromu): Bir olgu sunumu

KARAMAN A., Kahveci H.

Haseki Tip Bulteni , cilt.49, sa.2, ss.88-89, 2011 (Scopus, TRDizin)

47. A case of Goldenhar's syndrome and intracardiac aneurysm Goldenhar sendromu ve intrakardiyak anevrizmasi olan bir olgu

KARAMAN A., LALOĞLU F., Kahveci H.

Haseki Tip Bulteni , cilt.49, sa.2, ss.90-92, 2011 (Scopus, TRDizin)

48. Pierre robin syndrome: Case report Pi̇erre robi̇n sendromu

KARAMAN A., LALOĞLU F., Kahveci H.

SENDROM , cilt.23, sa.4-6, ss.47-48, 2011 (Scopus)

49. Klippel-Feil syndrome and Dandy-Walker malformation

KARAMAN A., Kahveci H.

Genetic Counseling , cilt.22, sa.4, ss.411-415, 2011 (SCI-Expanded, Scopus)

50. Unusual acrofacial dysostosis with severe limb defects: A new syndrome

KARAMAN A., Kahveci H.

Genetic Counseling , cilt.22, sa.3, ss.249-253, 2011 (SCI-Expanded, Scopus)

51. A boy with weyers-like ulnar ray/oligodactyly reduction limb defects and split hand malformation: Case report

Tos T., KARAMAN A., Gül D.

Genetic Counseling , cilt.22, sa.3, ss.245-248, 2011 (SCI-Expanded, Scopus)

52. Greig cephalopolysyndactyly syndrome: A case report Greig sefalopolisindaktili sendromu: Bir olgu sunumu

KARAMAN A., Kahveci H., LALOĞLU F.

Guncel Pediatri , cilt.9, sa.1, ss.47-49, 2011 (Scopus, TRDizin)

53. A rare case of monosomy 18p: Translocation between chromosomes 18 and 21

Tos T., KARAMAN A., Aycan Z., Tükün A.

Genetic Counseling , cilt.22, sa.2, ss.227-231, 2011 (SCI-Expanded, Scopus)

54. Comet assay and analysis of micronucleus formation in patients with rheumatoid arthritis

KARAMAN A., BİNİCİ D. N., ALKAN MELİKOĞLU M.

Mutation Research - Genetic Toxicology and Environmental Mutagenesis , cilt.721, sa.1, ss.1-5, 2011 (SCI-Expanded, Scopus)

55. Poland syndrome: A case report Poland sendromu: Bir olgu sunumu

Tos T., KARAMAN A., Perçin F., Koçak H.

Haseki Tip Bulteni , cilt.49, sa.1, ss.37-38, 2011 (Scopus, TRDizin)

56. A 45-year old man with cutaneous and subcutaneous masses of varying size

KARAMAN A., BİNİCİ D. N.

Marmara Medical Journal , cilt.24, sa.1, ss.83-84, 2011 (Scopus, TRDizin)

57. Oro-facio-digital syndrome type 1: Case report Oro-fasio-dijital sendrom tip 1: Olgu sunumu

KARAMAN A., Kahveci H., Biyik Y. Ç.

Medical Journal of Bakirkoy , cilt.7, sa.3, ss.120-121, 2011 (Scopus, TRDizin)

58. Genetic alterations in gastric precancerous lesions

KARAMAN A., Eşrefkabalar M., Nasir Binic D., Öztürk C., Pirim I.

Genetic Counseling , cilt.21, sa.4, ss.439-450, 2010 (SCI-Expanded, Scopus)

59. Medical problems in children with down syndrome in the erzurum area of Turkey

KARAMAN A.

Genetic Counseling , cilt.21, sa.4, ss.385-395, 2010 (SCI-Expanded, Scopus)

60. A male newborn infant with FATCO syndrome (fibular aplasia, tibial campomeua and oligodactyly): A case report

KARAMAN A., Kahveci H.

Genetic Counseling , cilt.21, sa.3, ss.285-288, 2010 (SCI-Expanded, Scopus)

61. Genomic instability in patients with Barrett's esophagus

KARAMAN A., BİNİCİ D. N., KABALAR M. E., KOCA T., DURSUN H.

Cancer Genetics and Cytogenetics , cilt.201, sa.2, ss.88-93, 2010 (SCI-Expanded, Scopus)

62. A case with balanced reciprocal translocation t(5;11)(q32;q24.2) and situs inversus viscerum

KARAMAN A., BİNİCİ D. N., Güneş N., Doru I., KABALAR M. E., Kurt A.

Genetic Counseling , cilt.21, sa.2, ss.237-242, 2010 (SCI-Expanded, Scopus)

63. Exposure to bitumen fumes and genotoxic effects on Turkish asphalt workers

KARAMAN A., Pirim I.

Clinical Toxicology , cilt.47, sa.4, ss.321-326, 2009 (SCI-Expanded, Scopus)

64. Sister chromatid exchange and micronucleus studies in patients with Behçet's disease

KARAMAN A., Kadi M., KARA F.

Journal of Cutaneous Pathology , cilt.36, sa.8, ss.831-837, 2009 (SCI-Expanded, Scopus)

65. Caroli's disease: A case report Caroli hastaliǧi: Bir olgu sunumu

KARAMAN A., BİNİCİ D. N., Doru I.

Goztepe Tip Dergisi , cilt.24, sa.2, ss.92-94, 2009 (Scopus, TRDizin)

66. Genomic damage in patients with chronic renal failure

KARAMAN A., Keskinler F.

Turkiye Klinikleri Journal of Medical Sciences , cilt.29, sa.6, ss.1392-1397, 2009 (SCI-Expanded, Scopus)

67. Oculocutaneus Albinism Okülokutanöz albinizim

KARAMAN A., Öztürk C.

Goztepe Tip Dergisi , cilt.23, sa.4, ss.149-155, 2008 (Scopus, TRDizin)

68. Micronucleus analysis in patients with colorectal adenocarcinoma and colorectal polyps

KARAMAN A., BİNİCİ D. N., KABALAR M. E., Çalikuşu Z.

World Journal of Gastroenterology , cilt.14, sa.44, ss.6835-6839, 2008 (SCI-Expanded, Scopus)

69. Intraperitoneal dedifferentiated liposarcoma: A case report

KARAMAN A., KABALAR M. E., Özcan Ö., KOCA T., BİNİCİ D. N.

World Journal of Gastroenterology , cilt.14, sa.38, ss.5927-5929, 2008 (SCI-Expanded, Scopus)

70. Sister chromatid exchange analysis in patients with psoriasis

KARAMAN A., Aliaǧaoǧlu C., Pirim I.

Experimental Dermatology , cilt.17, sa.6, ss.524-529, 2008 (SCI-Expanded, Scopus)

71. Alteration of sister chromatid exchange frequencies in gastric cancer and chronic atrophic gastritis patients with and without H pylori infection

KARAMAN A., BİNİCİ D. N., KABALAR M. E., DURSUN H., Kurt A.

World Journal of Gastroenterology , cilt.14, sa.16, ss.2534-2539, 2008 (SCI-Expanded, Scopus)

72. Bardet-Biedl syndrome Bardet-Biedl sendromu

KARAMAN A., Öztürk C.

Goztepe Tip Dergisi , cilt.23, sa.1, ss.37-40, 2008 (Scopus, TRDizin)

73. Double aneuploidy in a Turkish child: Down-Klinefelter syndrome

KARAMAN A., Kabalar E.

Congenital Anomalies , cilt.48, sa.1, ss.45-47, 2008 (Scopus)

74. Oculocutaneous albinism type 1A: A case report

KARAMAN A.

Dermatology Online Journal , cilt.14, sa.11, 2008 (Scopus)

75. Bardet-Biedl syndrome: A case report

KARAMAN A.

Dermatology Online Journal , cilt.14, sa.1, 2008 (Scopus)

76. Rubinstein-Taybi syndrome Rubinstein-Taybi sendromu

KARAMAN A.

SENDROM , cilt.18, sa.11, ss.89-90, 2006 (Scopus)

77. Frequency of sister chromatid exchanges in the lymphocytes of patients with atopic dermatitis

KARAMAN A., Aliaǧaoǧlu C.

Journal of Dermatology , cilt.33, sa.9, ss.596-602, 2006 (SCI-Expanded, Scopus)

78. A case with amniotic rupture sequence Bir amniyotik rüptür sekans olgusu

KARAMAN A., Kurt A., Pirim I.

Turkiye Klinikleri Journal of Medical Sciences , cilt.26, sa.1, ss.87-89, 2006 (Scopus)

79. Waardenburg syndrome type 1

KARAMAN A., Aliagaoglu C.

Dermatology Online Journal , cilt.12, sa.3, 2006 (Scopus)

80. Overview of neural tuba defects Nöral tüp defektlerinin gözden geçirilmesi

KARAMAN A.

SENDROM , cilt.17, sa.11, ss.97-101, 2005 (Scopus)

81. A case with craniofrontonasal dysplasia Kraniofrontonazal displazi

KARAMAN A., Bakan V.

SENDROM , cilt.17, sa.5, ss.105-106, 2005 (Scopus)

82. The functional classification of oncogenes and examples of malignancies associated with oncogenes Onkogenlerin fonksiyonel siniflandirmasi ve onkogenlerle ilişkili habaset örnekleri

KARAMAN A.

SENDROM , cilt.15, sa.8, ss.56-62, 2003 (Scopus)

83. The affect of tumour suppressor genes at cancer Kanserde tümör supresör genlerin etkisi

KARAMAN A.

SENDROM , cilt.15, sa.2, ss.71-77, 2003 (Scopus)

Yayınlar & Eserler

Yayın

Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Proje