| Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study TFMFS Group Medicine (Baltimore) 84 (1), 1-11, 2005 | 1224 | 2005 |
| Genotype–phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: evidence for mutation-independent amyloidosis F Yalçınkaya, N Cakar, M Mısırlıoğlu, N Tümer, N Akar, M Tekin, H Taştan, ... Rheumatology 39 (1), 67-72, 2000 | 313 | 2000 |
| A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis H Witt, M Sahin-Tóth, O Landt, JM Chen, T Kähne, JPH Drenth, Z Kukor, ... Nature genetics 38 (6), 668-673, 2006 | 294 | 2006 |
| Phylogeographic analysis of haplogroup E3b (E-M215) Y chromosomes reveals multiple migratory events within and out of Africa F Cruciani, R La Fratta, P Santolamazza, D Sellitto, R Pascone, P Moral, ... The American Journal of Human Genetics 74 (5), 1014-1022, 2004 | 292 | 2004 |
| Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis … B Simone, V De Stefano, E Leoncini, J Zacho, I Martinelli, J Emmerich, ... European journal of epidemiology 28, 621-647, 2013 | 261 | 2013 |
| Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations A Figus, A Angius, G Loudianos, C Bertini, V Dessì, A Loi, M Deiana, ... American journal of human genetics 57 (6), 1318, 1995 | 224 | 1995 |
| MEFV mutations in Turkish patients suffering from familial Mediterranean fever N Akar, M Misiroglu, F Yalcinkaya, E Akar, N Cakar, N Tümer, M Akcakus, ... Human mutation 15 (1), 118-119, 2000 | 200 | 2000 |
| Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe F Di Giacomo, F Luca, LO Popa, N Akar, N Anagnou, J Banyko, R Brdicka, ... Human genetics 115, 357-371, 2004 | 198 | 2004 |
| Frequency of factor V (1691 G→ A) mutation in Turkish population N Akar, E Akar, G Dalgin, A Sözüöz, K Ömürlü, S Cin Thrombosis and haemostasis 78 (12), 1527-1528, 1997 | 179 | 1997 |
| Common mutations at the homocysteine metabolism pathway and pediatric stroke N Akar, E Akar, D Özel, G Deda, T Sipahi Thrombosis Research 102 (2), 115-120, 2001 | 152 | 2001 |
| Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia M Tekin, BÖ Hişmi, S Fitoz, H Özdağ, FB Cengiz, A Sırmacı, I Aslan, ... The American Journal of Human Genetics 80 (2), 338-344, 2007 | 147 | 2007 |
| Prothrombin gene 20210 G‐A mutation in the Turkish population N Akar, M Misirlioglu, E Akar, F Avcu, A Yalçin, A Sözüöz American journal of hematology 58 (3), 249-249, 1998 | 137 | 1998 |
| Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis MBAJ KeiJzer, M Den Heijer, HJ Blom, GMJ Bos, HPJ Willems, ... Thrombosis and haemostasis 88 (11), 723-728, 2002 | 136 | 2002 |
| Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever‐associated vasculitis M Tekin, F Yalcinkaya, N Tumer, N Akar, M Misirlioǧlu, N Çakar2 Acta Paediatrica 89 (2), 177-182, 2000 | 129 | 2000 |
| Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations G Loudianos, V Dessi, M Lovicu, A Angius, B Altuntas, R Giacchino, ... Journal of medical genetics 36 (11), 833-836, 1999 | 127 | 1999 |
| Further delineation of the molecular pathology of Wilson disease in the Mediterranean population G Loudianos, V Dessì, M Lovicu, A Angius, A Nurchi, GC Sturniolo, ... Human mutation 12 (2), 89-94, 1998 | 115 | 1998 |
| Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa F Yalçınkaya, ZB Özçakar, Ö Kasapçopur, A Öztürk, N Akar, A Bakkaloğlu, ... The Journal of pediatrics 151 (6), 675-678, 2007 | 111 | 2007 |
| Familial Mediterranean fever—amyloidosis and the Val726Ala mutation F Yalçinkaya, N Akar, M Misirlioğlu New England Journal of Medicine 338 (14), 993-994, 1998 | 111 | 1998 |
| Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians M Tekin, N Akar, Ş Cin, S Blanton, X Xia, X Liu, W Nance, A Pandya Human genetics 108, 385-389, 2001 | 109 | 2001 |
| Effect of metylenetetrahydrofolate reductase 677 CT, 1298 AC, and 1317 TC on factor V 1691 mutation in Turkish deep vein thrombosis patients N Akar, E Akar, R Akçay, F Avcu, A Yalcin, S Cin Thrombosis Research 97 (3), 163-167, 2000 | 109 | 2000 |
Ece AkarAnkara UniversityVerified email at medicine.ankara.edu.tr