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Items: 1 to 50 of 97

1.

Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region.

Tuğ E, Ergün MA, Perçin EF.

Turk J Pediatr. 2018;60(1):94-98. doi: 10.24953/turkjped.2018.01.015.

2.

Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome.

Kayhan G, Ergun MA, Ergun SG, Kula S, Percin FE.

Genet Test Mol Biomarkers. 2018 Aug;22(8):474-480. doi: 10.1089/gtmb.2017.0286. Epub 2018 Jul 26.

PMID:
30048161
3.

Single-Nucleotide Polymorphisms in IL23R-IL12RB2 (rs1495965) Are Highly Prevalent in Patients with Behcet's Uveitis, and Vary between Populations.

Kramer M, Hasanreisoglu M, Weiss S, Kumova D, Schaap-Fogler M, Guntekin-Ergun S, Ozdek S, Gurelik G, Ergün MA, Goldenberg-Cohen N, Cohen Y.

Ocul Immunol Inflamm. 2018 May 24:1-8. doi: 10.1080/09273948.2018.1467463. [Epub ahead of print]

PMID:
29792538
4.

The relation between isolated micropenis in childhood with CAG and GGN repeat polymorphisms in the androgen receptor gene

Tuğ E, Güntekin Ergün S, Ergün MA, Dilek FN, Perçin EF.

Turk J Med Sci. 2018 Apr 30;48(2):430-434. doi: 10.3906/sag-1710-183.

PMID:
29714466
5.

Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing

Bakır A, Yirmibeş Karaoğuz M, Perçin FE, Tuğ E, Cinaz P, Ergün MA.

Turk J Med Sci. 2018 Apr 30;48(2):386-390. doi: 10.3906/sag-1711-74.

PMID:
29714459
6.

The University of Wisconsin Breast Cancer Epidemiology Simulation Model: An Update.

Alagoz O, Ergun MA, Cevik M, Sprague BL, Fryback DG, Gangnon RE, Hampton JM, Stout NK, Trentham-Dietz A.

Med Decis Making. 2018 Apr;38(1_suppl):99S-111S. doi: 10.1177/0272989X17711927.

PMID:
29554470
7.

Comparing CISNET Breast Cancer Incidence and Mortality Predictions to Observed Clinical Trial Results of Mammography Screening from Ages 40 to 49.

van den Broek JJ, van Ravesteyn NT, Mandelblatt JS, Huang H, Ergun MA, Burnside ES, Xu C, Li Y, Alagoz O, Lee SJ, Stout NK, Song J, Trentham-Dietz A, Plevritis SK, Moss SM, de Koning HJ.

Med Decis Making. 2018 Apr;38(1_suppl):140S-150S. doi: 10.1177/0272989X17718168.

PMID:
29554468
8.

Using Collaborative Simulation Modeling to Develop a Web-Based Tool to Support Policy-Level Decision Making About Breast Cancer Screening Initiation Age.

Burnside ES, Lee SJ, Bennette C, Near AM, Alagoz O, Huang H, van den Broek JJ, Kim JY, Ergun MA, van Ravesteyn NT, Stout NK, de Koning HJ, Mandelblatt JS.

MDM Policy Pract. 2017 Jul;2. doi: 10.1177/2381468317717982. Epub 2017 Jul 8.

9.

Association of Screening and Treatment With Breast Cancer Mortality by Molecular Subtype in US Women, 2000-2012.

Plevritis SK, Munoz D, Kurian AW, Stout NK, Alagoz O, Near AM, Lee SJ, van den Broek JJ, Huang X, Schechter CB, Sprague BL, Song J, de Koning HJ, Trentham-Dietz A, van Ravesteyn NT, Gangnon R, Chandler Y, Li Y, Xu C, Ergun MA, Huang H, Berry DA, Mandelblatt JS.

JAMA. 2018 Jan 9;319(2):154-164. doi: 10.1001/jama.2017.19130. Erratum in: JAMA. 2018 Feb 20;319(7):724.

10.

Comparative effectiveness of incorporating a hypothetical DCIS prognostic marker into breast cancer screening.

Trentham-Dietz A, Ergun MA, Alagoz O, Stout NK, Gangnon RE, Hampton JM, Dittus K, James TA, Vacek PM, Herschorn SD, Burnside ES, Tosteson ANA, Weaver DL, Sprague BL.

Breast Cancer Res Treat. 2018 Feb;168(1):229-239. doi: 10.1007/s10549-017-4582-0. Epub 2017 Nov 28.

PMID:
29185118
11.

Effect of Time to Diagnostic Testing for Breast, Cervical, and Colorectal Cancer Screening Abnormalities on Screening Efficacy: A Modeling Study.

Rutter CM, Kim JJ, Meester RGS, Sprague BL, Burger EA, Zauber AG, Ergun MA, Campos NG, Doubeni CA, Trentham-Dietz A, Sy S, Alagoz O, Stout N, Lansdorp-Vogelaar I, Corley DA, Tosteson ANA.

Cancer Epidemiol Biomarkers Prev. 2018 Feb;27(2):158-164. doi: 10.1158/1055-9965.EPI-17-0378. Epub 2017 Nov 17.

PMID:
29150480
12.

Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.

Kayhan G, Yılmaz Demirci N, Turktas H, Ergun MA.

Genet Test Mol Biomarkers. 2017 Oct;21(10):632-634. doi: 10.1089/gtmb.2017.0070. Epub 2017 Aug 14.

PMID:
28805452
13.

Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey.

Kan Karaer D, Ergün MA, Ruhi HI, Öztürk J, Kara H, Reisoğlu Çakmak D, Aydoğmuş T, Perçin EF.

Turk J Med Sci. 2017 Jun 12;47(3):973-978. doi: 10.3906/sag-1606-49.

PMID:
28618753
14.

LRP5-linked osteoporosis-pseudoglioma syndrome mimicking isolated microphthalmia.

Ergun SG, Akay GG, Ergun MA, Perçin EF.

Eur J Med Genet. 2017 Mar;60(3):200-204. doi: 10.1016/j.ejmg.2017.01.007. Epub 2017 Jan 19.

PMID:
28111184
15.

Investigation of CYP2D6 Gene Polymorphisms in Turkish Population.

Taskin B, Percin FE, Ergun MA.

Psychopharmacol Bull. 2016 Mar 1;46(1):67-72.

16.

Tailoring Breast Cancer Screening Intervals by Breast Density and Risk for Women Aged 50 Years or Older: Collaborative Modeling of Screening Outcomes.

Trentham-Dietz A, Kerlikowske K, Stout NK, Miglioretti DL, Schechter CB, Ergun MA, van den Broek JJ, Alagoz O, Sprague BL, van Ravesteyn NT, Near AM, Gangnon RE, Hampton JM, Chandler Y, de Koning HJ, Mandelblatt JS, Tosteson AN; Breast Cancer Surveillance Consortium and the Cancer Intervention and Surveillance Modeling Network.

Ann Intern Med. 2016 Nov 15;165(10):700-712. doi: 10.7326/M16-0476. Epub 2016 Aug 23.

17.

CFH Y402H and VEGF Polymorphisms and Anti-VEGF Treatment Response in Exudative Age-Related Macular Degeneration.

Kepez Yildiz B, Ozdek S, Ergun MA, Ergun S, Yaylacioglu Tuncay F, Elbeg S.

Ophthalmic Res. 2016;56(3):132-8. doi: 10.1159/000446186. Epub 2016 Jul 13.

PMID:
27404493
18.

The effect of CYP2C9 and VKORC1 genetic polymorphisms on warfarin dose requirements in a pediatric population.

Dilge Taşkın B, Kula S, Ergün MA, Altun D, Olguntürk R, Tunaoğlu FS, Oğuz AD, Gürsel T.

Anatol J Cardiol. 2016 Oct;16(10):791-796. doi: 10.14744/AnatolJCardiol.2015.6150. Epub 2016 Jan 25.

19.

Association of polymorphisms in APOE and LOXL1 with pseudoexfoliation syndrome and pseudoexfoliation glaucoma in a Turkish population.

Yaylacioğlu Tuncay F, Aktaş Z, Ergün MA, Ergün SG, Hasanreisoğlu M, Hasanreisoğlu B.

Ophthalmic Genet. 2017 Jan-Feb;38(1):95-97. doi: 10.3109/13816810.2015.1126617. Epub 2016 Mar 30. No abstract available.

PMID:
27028259
20.

Analysis of genetics and risk factors of Alzheimer's Disease.

Panpalli Ates M, Karaman Y, Guntekin S, Ergun MA.

Neuroscience. 2016 Jun 14;325:124-31. doi: 10.1016/j.neuroscience.2016.03.051. Epub 2016 Mar 26.

PMID:
27026590
21.

A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION.

Saat H, Soysal Y, Kurtgoz S, Ergun MA, Percin EF.

Genet Couns. 2015;26(4):401-7.

PMID:
26852510
22.

Collaborative Modeling of the Benefits and Harms Associated With Different U.S. Breast Cancer Screening Strategies.

Mandelblatt JS, Stout NK, Schechter CB, van den Broek JJ, Miglioretti DL, Krapcho M, Trentham-Dietz A, Munoz D, Lee SJ, Berry DA, van Ravesteyn NT, Alagoz O, Kerlikowske K, Tosteson AN, Near AM, Hoeffken A, Chang Y, Heijnsdijk EA, Chisholm G, Huang X, Huang H, Ergun MA, Gangnon R, Sprague BL, Plevritis S, Feuer E, de Koning HJ, Cronin KA.

Ann Intern Med. 2016 Feb 16;164(4):215-25. doi: 10.7326/M15-1536. Epub 2016 Jan 12.

23.

MECP2 DUPLICATION SYNDROME WITH ADDITIONAL FINDINGS.

Tug E, Ergun MA, Percin EF.

Genet Couns. 2016;27(4):471-478.

PMID:
30226965
24.

SUBMICROSCOPIC DUPLICATION OF 8q24.3 REGION IS A POTENTIAL CANDIDATE FOR DISORDERS OF SEX DEVELOPMENT.

Dilek FN, Perçin EF, Kayserili H, Ergün MA, Saka N.

Genet Couns. 2016;27(3):385-392.

PMID:
30204968
25.

Using Active Learning for Speeding up Calibration in Simulation Models.

Cevik M, Ergun MA, Stout NK, Trentham-Dietz A, Craven M, Alagoz O.

Med Decis Making. 2016 Jul;36(5):581-93. doi: 10.1177/0272989X15611359. Epub 2015 Oct 15.

26.

The role of interleukin-6 and interleukin-8 gene polymorphisms in non-alcoholic steatohepatitis.

Cengiz M, Yasar DG, Ergun MA, Akyol G, Ozenirler S.

Hepat Mon. 2014 Dec 24;14(12):e24635. doi: 10.5812/hepatmon.24635. eCollection 2014 Dec.

27.

National undergraduate medical core curriculum in Turkey: evaluation of residents.

Budakoğlu Iİ, Coşkun O, Ergün MA.

Balkan Med J. 2014 Mar;31(1):23-8. doi: 10.5152/balkanmedj.2013.9145. Epub 2013 Sep 27.

28.
29.

Does hyaluronic acid decrease the apoptotic effect of bupivacaine?

Güngör İ, Yılmaz A, Ergün MA, Öztürk AM, Kaya K.

Eklem Hastalik Cerrahisi. 2014;25(2):102-6. doi: 10.5606/ehc.2014.22.

30.

Ketamine is toxic to chondrocyte cell cultures.

Ozturk AM, Ergun MA, Demir T, Gungor I, Yilmaz A, Kaya K.

Bone Joint J. 2014 Jul;96-B(7):989-94. doi: 10.1302/0301-620X.96B7.33005.

PMID:
24986956
31.

Twenty-Four Genes are Upregulated in Patients with Hypospadias.

Karabulut R, Turkyilmaz Z, Sonmez K, Kumas G, Ergun S, Ergun M, Basaklar A.

Balkan J Med Genet. 2013 Dec;16(2):39-44. doi: 10.2478/bjmg-2013-0030.

32.

Mitotic stability of small supernumerary marker chromosomes: a study based on 93 immortalized cell lines.

Spittel H, Kubek F, Kreskowski K, Ziegler M, Klein E, Hamid AB, Kosyakova N, Radhakrishnan G, Junge A, Kozlowski P, Schulze B, Martin T, Huhle D, Mehnert K, Rodríguez L, Ergun MA, Sarri C, Militaru M, Stipoljev F, Tittelbach H, Vasheghani F, de Bello Cioffi M, Hussein SS, Fan X, Volleth M, Liehr T.

Cytogenet Genome Res. 2014;142(3):151-60. doi: 10.1159/000360776. Epub 2014 Apr 1.

33.

Formation of a familial ring chromosome 18 investigated by SNP-array analysis.

Balci S, Zschocke J, Kotzot D, Ergün MA, Spreiz A.

Am J Med Genet A. 2014 Jul;164A(7):1854-6. doi: 10.1002/ajmg.a.36496. Epub 2014 Mar 26. No abstract available.

PMID:
24677800
34.

Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.

Tuğ E, Yirmibeş Karaoğuz M, Kayhan G, Ergün MA, Perçin FE.

Am J Med Genet A. 2014 Jul;164A(7):1770-6. doi: 10.1002/ajmg.a.36495. Epub 2014 Mar 26. Review.

PMID:
24677787
35.

Bio-engineered synovial membrane to prevent tendon adhesions in rabbit flexor tendon model.

Baymurat AC, Ozturk AM, Yetkin H, Ergun MA, Helvacıoglu F, Ozkızılcık A, Tuzlakoğlu K, Şener EE, Erdogan D.

J Biomed Mater Res A. 2015 Jan;103(1):84-90. doi: 10.1002/jbm.a.35151. Epub 2014 Mar 20.

PMID:
24616375
36.

Epilepsy in Aicardi-Goutières syndrome.

Ramantani G, Maillard LG, Bast T, Husain RA, Niggemann P, Kohlhase J, Hertzberg C, Ungerath K, Innes MA, Walkenhorst H, Bevot A, von Stülpnagel C, Thomas K, Niemann F, Ergun MA, Tacke U, Häusler M, Ikonomidou C, Korinthenberg R, Lee-Kirsch MA.

Eur J Paediatr Neurol. 2014 Jan;18(1):30-7. doi: 10.1016/j.ejpn.2013.07.005. Epub 2013 Sep 5.

PMID:
24011626
37.

Comparison of radiation-induced damage between CT angiography and conventional coronary angiography.

Sahinarslan A, Erbas G, Kocaman SA, Bas D, Akyel A, Karaer D, Ergun MA, Arac M, Boyaci B.

Acta Cardiol. 2013 Jun;68(3):291-7.

PMID:
23882875
38.

The evaluation of long-term effects of ionizing radiation through measurement of current sister chromatid exchange (SCE) rates in radiology technologists, compared with previous SCE values.

Tug E, Kayhan G, Kan D, Guntekin S, Ergun MA.

Mutat Res. 2013 Sep 18;757(1):28-30. doi: 10.1016/j.mrgentox.2013.04.025. Epub 2013 Jul 15.

PMID:
23867852
39.

Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings.

Kayhan G, Cavdarli B, Yirmibes Karaoguz M, Percin EF, Oztürk Kaymak A, Biri A, Ergun MA.

Gene. 2013 Jul 25;524(2):355-60. doi: 10.1016/j.gene.2013.04.053. Epub 2013 May 1.

PMID:
23644025
40.

Bupivacaine and levobupivacaine induce apoptosis in rat chondrocyte cell cultures at ultra-low doses.

Gungor I, Yilmaz A, Ozturk AM, Ergun MA, Menevse S, Kaya K.

Eur J Orthop Surg Traumatol. 2014 Apr;24(3):291-5. doi: 10.1007/s00590-013-1202-5. Epub 2013 Mar 17.

PMID:
23503969
41.

Plasma levels and distribution of gene polymorphisms of factor VII in Turkish population.

Turfan M, Poyraz F, Kaymak AÖ, Ergun MA, Tavil Y, Gursel T, Abaci A.

Clin Appl Thromb Hemost. 2014 Mar;20(2):164-8. doi: 10.1177/1076029612459676. Epub 2012 Sep 9.

PMID:
22964781
42.

The prognostic role of hemochromatosis H63D allele in allogeneic hematopoietic stem cell transplantation.

Sucak GT, Yaşar DG, Yegin ZA, Ergün MA, Ozkurt ZN, Aki ŞZ, Güntekin S.

Ann Hematol. 2012 Aug;91(8):1281-7. doi: 10.1007/s00277-012-1428-z. Epub 2012 Feb 24.

PMID:
22362121
43.

Mutagenic and morphologic impacts of 1.8GHz radiofrequency radiation on human peripheral blood lymphocytes (hPBLs) and possible protective role of pre-treatment with Ginkgo biloba (EGb 761).

Esmekaya MA, Aytekin E, Ozgur E, Güler G, Ergun MA, Omeroğlu S, Seyhan N.

Sci Total Environ. 2011 Dec 1;410-411:59-64. doi: 10.1016/j.scitotenv.2011.09.036. Epub 2011 Oct 19.

PMID:
22014767
44.

A novel single point mutation of the LYST gene in two siblings with different phenotypic features of Chediak Higashi syndrome.

Kaya Z, Ehl S, Albayrak M, Maul-Pavicic A, Schwarz K, Kocak U, Ergun MA, Gursel T.

Pediatr Blood Cancer. 2011 Jul 1;56(7):1136-9. doi: 10.1002/pbc.22878. Epub 2011 Feb 4.

PMID:
21488161
45.

The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?

Karaer K, Ergun MA, Weise A, Ewers E, Liehr T, Kosyakova N, Mkrtchyan H.

Genet Couns. 2010;21(4):397-404.

PMID:
21290969
46.

A prenatal tertiary trisomy resulting from balanced maternal 8; 9 translocation.

Kayhan G, Ergün MA, Biri AA, Karaoğuz MY.

J Turk Ger Gynecol Assoc. 2011 Sep 1;12(3):183-5. doi: 10.5152/jtgga.2011.42. eCollection 2011.

47.

E-cadherin gene 3'-UTR C/T polymorphism in Turkish patients with nephrolithiasis.

Yilmaz A, Menevse S, Onaran M, Sen I, Ergun MA, Camtosun A, Kupeli B, Bozkirli I.

Mol Biol Rep. 2011 Nov;38(8):4931-4. doi: 10.1007/s11033-010-0635-8. Epub 2010 Dec 14.

PMID:
21161401
48.

Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth.

Balci S, Yuksel Konuk B, Atik F, Oguz AK, Ergun MA, Baltaci V, Kosyakova N, Liehr T.

Genet Couns. 2010;21(3):317-24.

PMID:
20964123
49.

A case with de novo inv dup del(8p) associated with dextrocardia and corpus callosum agenesis.

Ergün MA, Kula S, Karaer K, Perçin EF.

Pediatr Int. 2010 Oct;52(5):845-6. doi: 10.1111/j.1442-200X.2010.03181.x. No abstract available.

PMID:
20880309
50.

Duplication 4q associated with chronic cholestatic changes in liver biopsy.

Egritas O, Cavdarli B, Dalgic B, Ergun MA, Percin F, Ziegler M, Pohle B, Liehr T.

Eur J Med Genet. 2010 Nov-Dec;53(6):411-4. doi: 10.1016/j.ejmg.2010.08.008. Epub 2010 Sep 6.

PMID:
20826235

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