2012 William Allan Award Introduction: Uta Francke

Por Özçelik, Tayfun
Publicado em 2013

Medical genetics and genomic medicine in Turkey: a bright future at a new era in life sciences

Por Özçelik, Tayfun
Publicado no Mol Genet Genomic Med (2017)

Reply to Rivera

Por Lindgren, Valerie, Bryke, Christine R., Ozcelik, Tayfun, Yang-Feng, Teresa L., Francke, Uta
Publicado em 1993

Extreme Clonality in Lymphoblastoid Cell Lines with Implications for Allele Specific Expression Analyses

Por Plagnol, Vincent, Uz, Elif, Wallace, Chris, Stevens, Helen, Clayton, David, Ozcelik, Tayfun, Todd, John A.
Publicado em 2008

Skewed X-chromosome Inactivation in Scleroderma

Por Uz, Elif, Loubiere, Laurence S, Gadi, Vijayakrishna K., Ozbalkan, Zeynep, Stewart, Jeffrey, Nelson, J. Lee, Ozcelik, Tayfun
Publicado em 2008

Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans

Por Ozcelik, Tayfun, Akarsu, Nurten, Uz, Elif, Caglayan, Safak, Gulsuner, Suleyman, Onat, Onur Emre, Tan, Meliha, Tan, Uner
Publicado em 2008

Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion

Por Ozcelik, Tayfun, Akarsu, Nurten, Uz, Elif, Caglayan, Safak, Gulsuner, Suleyman, Onat, Onur Emre, Tan, Meliha, Tan, Uner
Publicado em 2008

Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ)

Por Doldur-Balli, Fusun, Ozel, Mehmet Neset, Gulsuner, Suleyman, Tekinay, Ayse B., Ozcelik, Tayfun, Konu, Ozlen, Adams, Michelle M.
Publicado no BMC Neurosci (2015)

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder

Por Patke, Alina, Murphy, Patricia J., Onat, Onur Emre, Krieger, Ana C., Özçelik, Tayfun, Campbell, Scott S., Young, Michael W.
Publicado no Cell (2017)

Endothelial progenitor cells display clonal restriction in multiple myeloma

Por Braunstein, Marc, Özçelik, Tayfun, Bağişlar, Sevgi, Vakil, Varsha, Smith, Eric LP, Dai, Kezhi, Akyerli, Cemaliye B, Batuman, Olcay A
Publicado em 2006

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

Por Emre Onat, Onur, Gulsuner, Suleyman, Bilguvar, Kaya, Nazli Basak, Ayse, Topaloglu, Haluk, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun
Publicado em 2013

Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases

Por Chabchoub, Ghazi, Uz, Elif, Maalej, Abdellatif, Mustafa, Chigdem A, Rebai, Ahmed, Mnif, Mouna, Bahloul, Zouheir, Farid, Nadir R, Ozcelik, Tayfun, Ayadi, Hammadi
Publicado em 2009

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis

Por Kanaan, Sami B., Onat, Onur E., Balandraud, Nathalie, Martin, Gabriel V., Nelson, J. Lee, Azzouz, Doua F., Auger, Isabelle, Arnoux, Fanny, Martin, Marielle, Roudier, Jean, Ozcelik, Tayfun, Lambert, Nathalie C.
Publicado no PLoS One (2016)

Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred

Por Gulsuner, Suleyman, Tekinay, Ayse Begum, Doerschner, Katja, Boyaci, Huseyin, Bilguvar, Kaya, Unal, Hilal, Ors, Aslihan, Onat, O. Emre, Atalar, Ergin, Basak, A. Nazli, Topaloglu, Haluk, Kansu, Tulay, Tan, Meliha, Tan, Uner, Gunel, Murat, Ozcelik, Tayfun
Publicado em 2011

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease

Por Unal Gulsuner, Hilal, Gulsuner, Suleyman, Mercan, Fatma Nazli, Onat, Onur Emre, Walsh, Tom, Shahin, Hashem, Lee, Ming K., Dogu, Okan, Kansu, Tulay, Topaloglu, Haluk, Elibol, Bulent, Akbostanci, Cenk, King, Mary-Claire, Ozcelik, Tayfun, Tekinay, Ayse B.
Publicado no Proc Natl Acad Sci U S A (2014)

Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor

Por Unal Gulsuner, Hilal, Gulsuner, Suleyman, Mercan, Fatma Nazli, Onat, Onur Emre, Walsh, Tom, Shahin, Hashem, Lee, Ming K., Dogu, Okan, Kansu, Tulay, Topaloglu, Haluk, Elibol, Bulent, Akbostanci, Cenk, King, Mary-Claire, Ozcelik, Tayfun, Tekinay, Ayse B.
Publicado no Proc Natl Acad Sci U S A (2015)

Mutations in RAD21 Disrupt Regulation of APOB in Patients with Chronic Intestinal Pseudo-obstruction

Por Bonora, Elena, Bianco, Francesca, Cordeddu, Lina, Bamshad, Michael, Francescatto, Ludmila, Dowless, Dustin, Stanghellini, Vincenzo, Cogliandro, Rosanna F., Lindberg, Greger, Mungan, Zeynel, Cefle, Kivanc, Ozcelik, Tayfun, Palanduz, Sukru, Ozturk, Sukru, Gedikbasi, Asuman, Gori, Alessandra, Pippucci, Tommaso, Graziano, Claudio, Volta, Umberto, Caio, Giacomo, Barbara, Giovanni, D'Amato, Mauro, Seri, Marco, Katsanis, Nicholas, Romeo, Giovanni, De Giorgio, Roberto
Publicado no Gastroenterology (2015)

Recessive LAMC3 mutations cause malformations of occipital cortical development

Por Barak, Tanyeri, Kwan, Kenneth Y, Louvi, Angeliki, Demirbilek, Veysi, Saygı, Serap, Tüysüz, Beyhan, Choi, Murim, Boyacı, Hüseyin, Doerschner, Katja, Zhu, Ying, Kaymakçalan, Hande, Yılmaz, Saliha, Bakırcıoğlu, Mehmet, Çağlayan, Ahmet Okay, Öztürk, Ali Kemal, Yasuno, Katsuhito, Brunken, William J, Atalar, Ergin, Yalçınkaya, Cengiz, Dinçer, Alp, Bronen, Richard A, Mane, Shrikant, Özçelik, Tayfun, Lifton, Richard P, Šestan, Nenad, Bilgüvar, Kaya, Günel, Murat
Publicado em 2011

Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649)

Por Knappskog, Stian, Gansmo, Liv B., Dibirova, Khadizha, Metspalu, Andres, Cybulski, Cezary, Peterlongo, Paolo, Aaltonen, Lauri, Vatten, Lars, Romundstad, Pål, Hveem, Kristian, Devilee, Peter, Evans, Gareth D., Lin, Dongxin, Camp, Guy Van, Manolopoulos, Vangelis G., Osorio, Ana, Milani, Lili, Ozcelik, Tayfun, Zalloua, Pierre, Mouzaya, Francis, Bliznetz, Elena, Balanovska, Elena, Pocheshkova, Elvira, Kučinskas, Vaidutis, Atramentova, Lubov, Nymadawa, Pagbajabyn, Titov, Konstantin, Lavryashina, Maria, Yusupov, Yuldash, Bogdanova, Natalia, Koshel, Sergey, Zamora, Jorge, Wedge, David C., Charlesworth, Deborah, Dörk, Thilo, Balanovsky, Oleg, Lønning, Per E.
Publicado no Oncotarget (2014)