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nejat akar
nejat akar
TOBB-ETU Medical School Pediatrics Department
Verified email at etu.edu.tr
Title
Cited by
Cited by
Year
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study
TFMFS Group
Medicine (Baltimore) 84 (1), 1-11, 2005
11522005
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
2972000
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
2872006
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
2872004
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
2382013
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
2241995
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
1902004
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
1882000
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
1721997
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, İ Aslan, ...
The American Journal of Human Genetics 80 (2), 338-344, 2007
1432007
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
1432001
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
1331998
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
1322002
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
1211999
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
1172000
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
1131998
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
1062000
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
1052007
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
1052001
Familial Mediterranean fever—amyloidosis and the Val726Ala mutation
F Yalçinkaya, N Akar, M Misirlioğlu
New England Journal of Medicine 338 (14), 993-994, 1998
1051998
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