Comment on Holger Breithaupt’s article ‘Losing them is not an option’ in EMBO reports, August 2001

Por Tolun, Aslihan
Publicado em 2001

Repair of Radiation-Induced Strand Breaks as Related to the Inducible Inhibitor of Postirradiation DNA Degradation

Por Tolun, Aslihan, Christensen, Ralph, Pollard, Ernest C.
Publicado em 1974

A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family

Por Yıldırım, Yeşerin, Kerem, Metin, Köroğlu, Çiğdem, Tolun, Aslıhan
Publicado em 2014

A novel recessive GUCY2D mutation causing cone–rod dystrophy and not Leber's congenital amaurosis

Por Ugur Iseri, Sibel A, Durlu, Yusuf K, Tolun, Aslihan
Publicado em 2010

Adult phenotype and further phenotypic variability in SRD5A3-CDG

Por Kara, Bülent, Ayhan, Özgecan, Gökçay, Gülden, Başboğaoğlu, Nurdan, Tolun, Aslıhan
Publicado em 2014

Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis

Por Corut, Ayse, Senyigit, Abdurrahman, Ugur, Sibel Aylin, Altin, Sedat, Ozcelik, Ugur, Calisir, Haluk, Yildirim, Zeki, Gocmen, Ayhan, Tolun, Aslihan
Publicado em 2006

A role of autophagy in spinocerebellar ataxia—Rare exception or general principle?

Por Burmeister, Margit, Lee, Jun-Hee, Schulman, Brenda A., Yapici, Zuhal, Tolun, Aslıhan, Juhasz, Gabor, Li, Jun Z., Klionsky, Daniel J.
Publicado no Autophagy (2016)

Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A

Por Kara, Bülent, Köroğlu, Çiğdem, Peltonen, Karita, Steinberg, Ruchama C, Maraş Genç, Hülya, Hölttä-Vuori, Maarit, Güven, Ayşe, Kanerva, Kristiina, Kotil, Tuğba, Solakoğlu, Seyhun, Zhou, You, Olkkonen, Vesa M, Ikonen, Elina, Laiho, Marikki, Tolun, Aslıhan
Publicado no Eur J Hum Genet (2017)

Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay

Por Kim, Myungjin, Sandford, Erin, Gatica, Damian, Qiu, Yu, Liu, Xu, Zheng, Yumei, Schulman, Brenda A, Xu, Jishu, Semple, Ian, Ro, Seung-Hyun, Kim, Boyoung, Mavioglu, R Nehir, Tolun, Aslıhan, Jipa, Andras, Takats, Szabolcs, Karpati, Manuela, Li, Jun Z, Yapici, Zuhal, Juhasz, Gabor, Lee, Jun Hee, Klionsky, Daniel J, Burmeister, Margit
Publicado no eLife (2016)

Large-scale recent expansion of European patrilineages shown by population resequencing

Por Batini, Chiara, Hallast, Pille, Zadik, Daniel, Delser, Pierpaolo Maisano, Benazzo, Andrea, Ghirotto, Silvia, Arroyo-Pardo, Eduardo, Cavalleri, Gianpiero L., de Knijff, Peter, Dupuy, Berit Myhre, Eriksen, Heidi A., King, Turi E., de Munain, Adolfo López, López-Parra, Ana M., Loutradis, Aphrodite, Milasin, Jelena, Novelletto, Andrea, Pamjav, Horolma, Sajantila, Antti, Tolun, Aslıhan, Winney, Bruce, Jobling, Mark A.
Publicado no Nat Commun (2015)

Localization of an Ataxia-Telangiectasia Gene to an −500-kb Interval on Chromosome 11q23.1: Linkage Analysis of 176 Families by an International Consortium

Por Lange, Ethan, Borresen, Anna-Lise, Chen, Xiaoguang, Chessa, Luciana, Chiplunkar, Sujata, Concannon, Patrick, Dandekar, Sugandha, Gerken, Steven, Lange, Kenneth, Liang, Teresa, McConville, Carmel, Polakow, Jeff, Porras, Oscar, Rotman, Galit, Sanal, Ozden, Sheikhavandi, Sepideh, Shiloh, Yosef, Sobel, Eric, Taylor, Malcolm, Telatar, Milhan, Teraoka, Sharon, Tolun, Aslihan, Udar, Nitin, Uhrhammer, Nancy, Vanagaite, Lina, Wang, Zhijun, Wapelhorst, Beth, Wright, Jocyndra, Yang, Huan-Ming, Yang, Lan, Ziv, Yael, Gatti, Richard A.
Publicado em 1995

The Y-Chromosome Tree Bursts into Leaf: 13,000 High-Confidence SNPs Covering the Majority of Known Clades

Por Hallast, Pille, Batini, Chiara, Zadik, Daniel, Maisano Delser, Pierpaolo, Wetton, Jon H., Arroyo-Pardo, Eduardo, Cavalleri, Gianpiero L., de Knijff, Peter, Destro Bisol, Giovanni, Dupuy, Berit Myhre, Eriksen, Heidi A., Jorde, Lynn B., King, Turi E., Larmuseau, Maarten H., López de Munain, Adolfo, López-Parra, Ana M., Loutradis, Aphrodite, Milasin, Jelena, Novelletto, Andrea, Pamjav, Horolma, Sajantila, Antti, Schempp, Werner, Sears, Matt, Tolun, Aslıhan, Tyler-Smith, Chris, Van Geystelen, Anneleen, Watkins, Scott, Winney, Bruce, Jobling, Mark A.
Publicado no Mol Biol Evol (2015)

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

Por Novarino, Gaia, Fenstermaker, Ali G., Zaki, Maha S., Hofree, Matan, Silhavy, Jennifer L., Heiberg, Andrew D., Abdellateef, Mostafa, Rosti, Basak, Scott, Eric, Mansour, Lobna, Masri, Amira, Kayserili, Hulya, Al-Aama, Jumana Y., Abdel-Salam, Ghada M. H., Karminejad, Ariana, Kara, Majdi, Kara, Bulent, Bozorgmehri, Bita, Ben-Omran, Tawfeg, Mojahedi, Faezeh, El Din Mahmoud, Iman Gamal, Bouslam, Naima, Bouhouche, Ahmed, Benomar, Ali, Hanein, Sylvain, Raymond, Laure, Forlani, Sylvie, Mascaro, Massimo, Selim, Laila, Shehata, Nabil, Al-Allawi, Nasir, Bindu, P.S., Azam, Matloob, Gunel, Murat, Caglayan, Ahmet, Bilguvar, Kaya, Tolun, Aslihan, Issa, Mahmoud Y., Schroth, Jana, Spencer, Emily G., Rosti, Rasim O., Akizu, Naiara, Vaux, Keith K., Johansen, Anide, Koh, Alice A., Megahed, Hisham, Durr, Alexandra, Brice, Alexis, Stevanin, Giovanni, Gabriel, Stacy B., Ideker, Trey, Gleeson, Joseph G.
Publicado em 2014

Y-Chromosomal Diversity in Europe Is Clinal and Influenced Primarily by Geography, Rather than by Language

Por Rosser, Zoë H. , Zerjal, Tatiana , Hurles, Matthew E. , Adojaan, Maarja , Alavantic, Dragan , Amorim, António , Amos, William , Armenteros, Manuel , Arroyo, Eduardo , Barbujani, Guido , Beckman, Gunhild , Beckman, Lars , Bertranpetit, Jaume , Bosch, Elena , Bradley, Daniel G. , Brede, Gaute , Cooper, Gillian , Côrte-Real, Helena B. S. M. , de Knijff, Peter , Decorte, Ronny , Dubrova, Yuri E. , Evgrafov, Oleg , Gilissen, Anja , Glisic, Sanja , Gölge, Mukaddes , Hill, Emmeline W. , Jeziorowska, Anna , Kalaydjieva, Luba , Kayser, Manfred , Kivisild, Toomas , Kravchenko, Sergey A. , Krumina, Astrida , Kučinskas, Vaidutis , Lavinha, João , Livshits, Ludmila A. , Malaspina, Patrizia , Maria, Syrrou , McElreavey, Ken , Meitinger, Thomas A. , Mikelsaar, Aavo-Valdur , Mitchell, R. John , Nafa, Khedoudja , Nicholson, Jayne , Nørby, Søren , Pandya, Arpita , Parik, Jüri , Patsalis, Philippos C. , Pereira, Luísa , Peterlin, Borut , Pielberg, Gerli , Prata, Maria João , Previderé, Carlo , Roewer, Lutz , Rootsi, Siiri , Rubinsztein, D. C. , Saillard, Juliette , Santos, Fabrício R. , Stefanescu, Gheorghe , Sykes, Bryan C. , Tolun, Aslihan , Villems, Richard , Tyler-Smith, Chris , Jobling, Mark A. 
Publicado em 2000

TBC1D24 genotype–phenotype correlation: Epilepsies and other neurologic features

Por Balestrini, Simona, Milh, Mathieu, Castiglioni, Claudia, Lüthy, Kevin, Finelli, Mattea J., Verstreken, Patrik, Cardon, Aaron, Stražišar, Barbara Gnidovec, Holder, J. Lloyd, Lesca, Gaetan, Mancardi, Maria M., Poulat, Anne L., Repetto, Gabriela M., Banka, Siddharth, Bilo, Leonilda, Birkeland, Laura E., Bosch, Friedrich, Brockmann, Knut, Cross, J. Helen, Doummar, Diane, Félix, Temis M., Giuliano, Fabienne, Hori, Mutsuki, Hüning, Irina, Kayserili, Hulia, Kini, Usha, Lees, Melissa M., Meenakshi, Girish, Mewasingh, Leena, Pagnamenta, Alistair T., Peluso, Silvio, Mey, Antje, Rice, Gregory M., Rosenfeld, Jill A., Taylor, Jenny C., Troester, Matthew M., Stanley, Christine M., Ville, Dorothee, Walkiewicz, Magdalena, Falace, Antonio, Fassio, Anna, Lemke, Johannes R., Biskup, Saskia, Tardif, Jessica, Ajeawung, Norbert F., Tolun, Aslihan, Corbett, Mark, Gecz, Jozef, Afawi, Zaid, Howell, Katherine B., Oliver, Karen L., Berkovic, Samuel F., Scheffer, Ingrid E., de Falco, Fabrizio A., Oliver, Peter L., Striano, Pasquale, Zara, Federico, Campeau, Phillipe M., Sisodiya, S.M.
Publicado no Neurology (2016)