A 2D mathematical model for tumor angiogenesis: The roles of certain cells in the extra cellular matrix by Pamuk, Serdal, Çay, İrem, Sazcı, Ali

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Pregnancy in Parkinson's disease with PARK2 mutations by Sazci, Ali, Idrisoglu, Halil Atilla

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Investigation of some variations of superoxide dismutase gene family in Turkish sporadic amyotrophic lateral sclerosis patients by Büyüköz, Melda, Sazci, Ali, Ergül, Emel, Idrisoglu, Halil Atilla

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Association of Nicotinamide-N-Methyltransferase Gene rs694539 Variant with Epilepsy by Sazci, Gensay, Sazci, Bilgen, Sazci, Ali, Idrisoglu, Halil Atilla

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Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia by Sozuguzel, Mavi Deniz, Sazci, Ali, Yildiz, Mustafa

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The rs2228570 Variant of the Vitamin D Receptor Gene is Associated with Essential Tremor by Sazci, Ali, Uren, Nihal, Idrisoglu, Halil Atilla, Ergul, Emel

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Nicotinamide-N-Methyltransferase gene rs694539 variant and migraine risk by Sazci, Ali, Sazci, Gensay, Sazci, Bilgen, Ergul, Emel, Idrisoglu, Halil Atilla

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Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischaemic stroke by Tuncer, Nese, Tuglular, Serhan, Kılıç, Gamze, Sazcı, Ali, Us, Önder, Kara, İhsan

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Association of nicotinamide-N-methyltransferase (NNMT) gene rs694539 variant with bipolar disorder by Sazci, Ali, Ozel, Mavi Deniz, Ergul, Emel, Onder, Mehmet Emin

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Methylenetetrahydrofolate reductase gene polymorphisms are associated with ischemic and hemorrhagic stroke: Dual effect of MTHFR polymorphisms C677T and A1298C by Sazci, Ali, Ergul, Emel, Tuncer, Nese, Akpinar, Gurler, Kara, Ihsan

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Using global team science to identify genetic parkinson's disease worldwide by Vollstedt, Eva‐Juliane, Klein, Christine, Ahmad‐Annuar, Azlina, Al‐Mubarak, Bashayer, Annesi, Grazia, Barber, Thomas R., Bardien, Soraya, Başak, A. Nazlı, Bhatia, Kailash, Binkofski, Ferdinand, Bozi, Maria, Brice, Alexis, Brighina, Laura, Brockmann, Kathrin, Brücke, Thomas, Chen‐Plotkin, Alice, Ju Chung, Sun, Clark, Lorraine, Corvol, Jean‐Christophe, Cosentino, Carlos, Cras, Patrick, Crosiers, David, De Michele, Giuseppe, De Rosa, Anna, Erer, Sevda, Ertan, Sibel, Farrer, Matthew, Fiala, Ondrej, Foroud, Tatiana, Friedman, Andrzej, Frigerio, Roberta, Garraux, Gaetan, Gomez‐Esteban, Juan Carlos, Hardy, John, Hassan, Anhar, Hedera, Peter, Hentati, Faycal, Inca‐Martinez, Miguel, Infante, Jon, Jankovic, Joseph, Jesús, Silvia, Kasten, Meike, Kataoka, Hiroshi, Kim, Yun Joong, Koziorowski, Dariusz, Krüger, Rejko, Krygowska‐Wajs, Anna, Kulisevsky, Jaime, Lai, Dongbing, Lang, Anthony, LeDoux, Mark, Lesage, Suzanne, Lim, Shen‐Yang, Lin, Chin‐Hsien, Lopera, Francisco, Lopez, Grisel, Lu, Chin‐Song, Lynch, Tim, Maraganore, Demetrius, Marder, Karen, Mazzetti, Pilar, Mirelman, Anat, Morris, Huw, Naito, Anna, Ozelius, Laurie J., Padmanabhan, Shalini, Paisán‐Ruiz, Coro, Petkovic, Sonja, Petrucci, Simona, Pimentel, Márcia, Pirker, Walter, Pulkes, Teeratorn, Puschmann, Andreas, Quattrone, Aldo, Sammler, Esther, Sazci, Ali, Schrag, Anette, Sharma, Manu, Sidransky, Ellen, Petersen, Maria Skaalum, Sue, Carolyn M., Swan, Matthew, Swanberg, Maria, Taba, Pille, Tan, Manuela, Tan, Ai Huey, Tan, Eng‐King, Tayebi, Nahid, Thaler, Avner, Thomas, Astrid, Toda, Tatsushi, Torres, Luis, Valente, Enza Maria, Van Broeckhoven, Christine, Wood, Nicholas W., Wszolek, Zbigniew K., Wu, Ruey‐Meei, Yoshino, Hiroyo, Zhang, Baorong, Zimprich, Alexander

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A novel missense mutation in the UBE2A gene causes intellectual disability in the large X‐linked family by Arslan Satılmış, Saide Betül, Kurt, Emin Emre, Akçay, Ebru Perim, Sazci, Ali, Ceylan, Ahmet Cevdet

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The comparison of VEGFR-1-binding domain of VEGF-A with modelled VEGF-C sheds light on receptor specificity by Kasap, Murat, Sazci, Ali

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Association of Apolipoprotein E Polymorphisms in Patients with Non-Alcoholic Steatohepatitis by Sazci, Ali, Akpinar, Gurler, Aygun, Cem, Ergul, Emel, Senturk, Omer, Hulagu, Sadettin

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Association of rs62063857 Variant of the Saitohin Gene with Parkinson’s Disease by Sonmez, Ezgi, Ozel, Mavi Deniz, Islek, Eylul Ece, Sazci, Ali, Idrisoglu, Halil Atilla

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TP53 Arg72Pro polymorphism in Turkish patients with sporadic amyotrophic lateral sclerosis by Ergul, Emel, Ozel, Mavi Deniz, Sazci, Ali, Idrisoglu, Halil Atilla

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Transcription factor 4 gene rs9960767 polymorphism in bipolar disorder by Ozel, Mavi Deniz, Onder, Mehmet Emin, Sazci, Ali

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Association of Saitohin Gene Rs62063857 Variant with Dementia by Sonmez, Ezgi, Ozel, Mavi D, Sazci, Ali, Ergul, Emel, Idrısoglu, Halil A

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The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants by Heckman, Michael G, Elbaz, Alexis, Soto-Ortolaza, Alexandra I, Serie, Daniel J, Aasly, Jan O, Annesi, Grazia, Auburger, Georg, Bacon, Justin A, Boczarska-Jedynak, Magdalena, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Dardiotis, Efthimios, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Ioannidis, John P.A, Jasinska-Myga, Barbara, Jeon, Beom S, Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A, Sohn, Young Ho, Stefanis, Leonidas, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J, Valente, Enza Maria, Vassilatis, Demetrios K, Vilariño-Güell, Carles, White, Linda R, Wirdefeldt, Karin, Wszolek, Zbigniew K, Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M, Farrer, Matthew J, Ross, Owen A

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Association of the nibrin gene (NBN) variants with breast cancer by UZUNOGLU, HAKAN, KORAK, TUGCAN, ERGUL, EMEL, UREN, NIHAL, SAZCI, ALI, UTKAN, N. ZAFER, KARGI, ERTUĞRUL, TRIYAKI, ÇAĞRI, YIRMIBESOGLU, OKTAY

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