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

le Tolun, Aslihan
Foilsithe 2001

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

le Tolun, Aslihan, Christensen, Ralph, Pollard, Ernest C.
Foilsithe 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

le Yıldırım, Yeşerin, Kerem, Metin, Köroğlu, Çiğdem, Tolun, Aslıhan
Foilsithe 2014

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

le Ugur Iseri, Sibel A, Durlu, Yusuf K, Tolun, Aslihan
Foilsithe 2010

Adult phenotype and further phenotypic variability in SRD5A3-CDG

le Kara, Bülent, Ayhan, Özgecan, Gökçay, Gülden, Başboğaoğlu, Nurdan, Tolun, Aslıhan
Foilsithe 2014

Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility

le Yıldırım, Yeşerin, Ouriachi, Toufik, Woehlbier, Ute, Ouahioune, Wahiba, Balkan, Mahmut, Malik, Sajid, Tolun, Aslıhan
Foilsithe in Eur J Hum Genet (2018)

A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

le Karacan, İlker, Diz Küçükkaya, Reyhan, Karakuş, Fatma Nur, Solakoğlu, Seyhun, Tolun, Aslıhan, Hançer, Veysel Sabri, Turanlı, Eda Tahir
Foilsithe in Turk J Haematol (2019)

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

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

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

le Burmeister, Margit, Lee, Jun-Hee, Schulman, Brenda A., Yapici, Zuhal, Tolun, Aslıhan, Juhasz, Gabor, Li, Jun Z., Klionsky, Daniel J.
Foilsithe in Autophagy (2016)

Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A

le 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
Foilsithe in Eur J Hum Genet (2017)

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

le 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
Foilsithe in eLife (2016)

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

le 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.
Foilsithe in 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

le 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.
Foilsithe 1995

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

le 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.
Foilsithe in Mol Biol Evol (2015)

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

le 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.
Foilsithe 2014

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

le 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. 
Foilsithe 2000

TBC1D24 genotype–phenotype correlation: Epilepsies and other neurologic features

le 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.
Foilsithe in Neurology (2016)