First Report of Two Rare Entities in a Family: 49,XXXXY and 45,X

Por Şahin, Yavuz, Özcan, Aysegül
Publicado no J Pediatr Genet (2017)

DiGeorge Syndrome Associated with Azoospermia: First case in the literature

Por Özcan, Ayşegül, Şahin, Yavuz
Publicado no Turk J Urol (2017)

Structural and Genomic Variation in Preterm Birth

Por Uzun, Alper, Sahin, Yavuz, Schuster, Jessica S., Zheng, Xiaojing, Ryckman, Kelli, Feingold, Eleanor, Padbury, James
Publicado no Pediatr Res (2016)

The relationship between estradiol-progesterone alterations after ovulation trigger and treatment success in intrauterine insemination cycles

Por Kutlu, Tayfun, Özkaya, Enis, Şanverdi, İlhan, Devranoğlu, Belgin, İpekçi, Cansu, Konukçu, Birsen, Şahin, Yavuz, Karateke, Ateş
Publicado no Turk J Obstet Gynecol (2016)

Non-invasive prediction of implantation window in controlled hyperstimulation cycles: Can the time from the menstrual day at embryo transfer to expected menstrual cycle give a clue...

Por Şanverdi, İlhan, Özkaya, Enis, Kutlu, Tayfun, Şenol, Taylan, Akalın, Munip, Sayar Akalın, Eda, Şahin, Yavuz, Karateke, Ateş
Publicado no Turk J Obstet Gynecol (2016)

Clinical analyses of successful and previously failed intracytoplasmic sperm injection cycle parameters in patients with poor ovarian reserve

Por Kutlu, Tayfun, Özkaya, Enis, Kumru, Pınar, Ayvacı, Habibe, Devranoğlu, Belgin, Sanverdi, İlhan, Şahin, Yavuz, Sağlam, Beyhan, Karateke, Ateş
Publicado no Turk J Obstet Gynecol (2017)

A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, “1033G>T”, at the SERPING1 gene

Por Ozkars, Mehmet Yasar, Keskın, Ozlem, Bayram, Nazan, Onay, Huseyin, Keskın, Mehmet, Bayram, Hasan, Sahın, Yavuz, Küçükosmanoğlu, Ercan, Kırık, Serkan
Publicado no Postepy Dermatol Alergol (2019)

Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide

Por Gonzaga-Jauregui, Claudia, Yesil, Gozde, Nistala, Harikiran, Gezdirici, Alper, Bayram, Yavuz, Nannuru, Kalyan C., Pehlivan, Davut, Yuan, Bo, Jimenez, Johanna, Sahin, Yavuz, Paine, Ingrid S., Akdemir, Zeynep Coban, Rajamani, Saathyaki, Staples, Jeffrey, Dronzek, John, Howell, Kristen, Fatih, Jawid M., Smaldone, Silvia, Schlesinger, Alan E., Ramírez, Norman, Cornier, Alberto S., Kelly, Melissa A., Haber, Robert, Chim, Shek Man, Nieman, Kristy, Wu, Nan, Walls, Johnathon, Poueymirou, William, Siao, Chia-Jen, Sutton, V. Reid, Williams, Marc S., Posey, Jennifer E., Gibbs, Richard A., Carlo, Simon, Tegay, David H., Economides, Aris N., Lupski, James R.
Publicado no Eur J Hum Genet (2020)

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

Por Pehlivan, Davut, Bayram, Yavuz, Gunes, Nilay, Coban Akdemir, Zeynep, Shukla, Anju, Bierhals, Tatjana, Tabakci, Burcu, Sahin, Yavuz, Gezdirici, Alper, Fatih, Jawid M., Gulec, Elif Yilmaz, Yesil, Gozde, Punetha, Jaya, Ocak, Zeynep, Grochowski, Christopher M., Karaca, Ender, Albayrak, Hatice Mutlu, Radhakrishnan, Periyasamy, Erdem, Haktan Bagis, Sahin, Ibrahim, Yildirim, Timur, Bayhan, Ilhan A., Bursali, Aysegul, Elmas, Muhsin, Yuksel, Zafer, Ozdemir, Ozturk, Silan, Fatma, Yildiz, Onur, Yesilbas, Osman, Isikay, Sedat, Balta, Burhan, Gu, Shen, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Tsiakas, Konstantinos, Hempel, Maja, Girisha, Katta Mohan, Gul, Davut, Posey, Jennifer E., Elcioglu, Nursel H., Tuysuz, Beyhan, Lupski, James R.
Publicado no Am J Hum Genet (2019)