BetterScholar BetterScholar
8
Role
Title
Level Year L/R
🐬 Urate‐induced immune programming: Consequences for gouty arthritis and hyperuricemia
Georgiana Cabău, T. Crișan, V. Klück, R. Popp, L. Joosten
7 2019
7
🐬
🐜 Convergent evolution in European and Rroma populations reveals pressure exerted by plague on Toll-like receptors
18 auth. H. Laayouni, M. Oosting, P. Luisi, M. Ioana, S. Alonso, I. Ricaño-Ponce, G. Trynka, A. Zhernakova, T. Plantinga, Shih-Chin Cheng, ... J. V. D. van der Meer, R. Popp, A. Sood, B. K. Thelma, C. Wijmenga, L. Joosten, J. Bertranpetit, M. Netea
6 2014
6
🐜
🐬 Genetic determination of irritable bowel syndrome.
C. Hoţoleanu, R. Popp, A. Trifa, L. Nedelcu, D. Dumitrascu
5 2008
5
🐬
🐢 MECOM, HBS1L‐MYB, THRB‐RARB, JAK2, and TERT polymorphisms defining the genetic predisposition to myeloproliferative neoplasms: A study on 939 patients
31 auth. A. Trifa, C. Bănescu, A. Bojan, Cristian M Voina, S. Popa, Simona Vișan, A. Ciubean, F. Tripon, D. Dima, V. Popov, Ș. Vesa, M. Andreescu, Tünde Török-Vistai, R. Mihaila, Nicoleta P. Berbec, ... I. Macarie, A. Colita, M. Iordache, A. Cătană, M. Farcas, C. Tomuleasa, K. Vasile, C. Truica, Adriana Todincă, Lavinia Pop-Muntean, R. Manolache, H. Bumbea, A. Vlădăreanu, M. Găman, C. Ciufu, R. Popp
5 2018
5
🐢
🐢 TERT rs2736100 A>C SNP and JAK2 46/1 haplotype significantly contribute to the occurrence of JAK2 V617F and CALR mutated myeloproliferative neoplasms – a multicentric study on 529 patients
25 auth. A. Trifa, C. Bănescu, Mihaela Tevet, A. Bojan, D. Dima, L. Urian, Tünde Török-Vistai, V. Popov, M. Zdrenghea, L. Petrov, A. Vasilache, Meilin Murat, D. Georgescu, M. Popescu, O. Pătrinoiu, ... M. Balea, R. Costache, E. Coleș, C. Saguna, Nicoleta P. Berbec, A. Vlădăreanu, R. Mihaila, H. Bumbea, A. Cucuianu, R. Popp
5 2016
5
🐢
🐢 The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms
8 auth. A. Trifa, A. Cucuianu, L. Petrov, L. Urian, M. Militaru, D. Dima, ... I. Pop, R. Popp
5 2010
5
🐢
🐜 Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania.
9 auth. C. Lazar, R. Popp, A. Trifa, C. Mocanu, G. Mihuț, C. Al-Khzouz, ... E. Tomescu, I. Figan, P. grigorescu-sido
4 2010
4
🐜
🐬 The Role of Oxidative Stress and Vascular Insufficiency in Primary Open Angle Glaucoma
A. Ster, R. Popp, F. Petrişor, C. Stan, V. Pop
4 2014
4
🐬