nejat akar
nejat akar
TOBB-ETU Tıp Fakültesi Çocuk Sağ ve Hastalıkları
Verified email at etu.edu.tr
Title
Cited by
Cited by
Year
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
2652004
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
2372006
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
2092000
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
2091995
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 (5), 357-371, 2004
1772004
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
1531997
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 (8), 621-647, 2013
1512013
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
1302000
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
1201998
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
1182007
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
1142001
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
1091999
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study
Turkish FMF Study Group
Medicine 84 (1), 1-11, 2005
1082005
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
1041998
Connexiná26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians
M Tekin, N Akar, ŞŘŘ Cin, S Blanton, X Xia, X Liu, W Nance, A Pandya
Human genetics 108 (5), 385-389, 2001
1022001
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
962000
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
952000
Factor V1691 GA, prothrombin 20210 GA, and methylenetetrahydrofolate reductase 677 CT variants in Turkish children with cerebral infarct
N Akar, E Akar, G Deda, T Sipahi, A Orsal
Journal of child neurology 14 (11), 749-751, 1999
871999
Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative mating
M Tekin, T Duman, G Boğoçlu, A İncesulu, E Çomak, I Ilhan, N Akar
Human mutation 21 (5), 552-553, 2003
842003
Effects of zinc supplementation on linear growth in beta‐thalassemia (A new approach)
A Arcasoy, A Cavdar, Ş Cin, J Erten, E Babacan, S Gözdasoglu, N Akar
American journal of hematology 24 (2), 127-136, 1987
801987
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