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

le Şahin, Yavuz, Özcan, Aysegül
Foilsithe in J Pediatr Genet (2017)

DiGeorge Syndrome Associated with Azoospermia: First case in the literature

le Özcan, Ayşegül, Şahin, Yavuz
Foilsithe in Turk J Urol (2017)

Structural and Genomic Variation in Preterm Birth

le Uzun, Alper, Sahin, Yavuz, Schuster, Jessica S., Zheng, Xiaojing, Ryckman, Kelli, Feingold, Eleanor, Padbury, James
Foilsithe in Pediatr Res (2016)

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

le Kutlu, Tayfun, Özkaya, Enis, Şanverdi, İlhan, Devranoğlu, Belgin, İpekçi, Cansu, Konukçu, Birsen, Şahin, Yavuz, Karateke, Ateş
Foilsithe in 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...

le Şanverdi, İlhan, Özkaya, Enis, Kutlu, Tayfun, Şenol, Taylan, Akalın, Munip, Sayar Akalın, Eda, Şahin, Yavuz, Karateke, Ateş
Foilsithe in Turk J Obstet Gynecol (2016)

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

le Kutlu, Tayfun, Özkaya, Enis, Kumru, Pınar, Ayvacı, Habibe, Devranoğlu, Belgin, Sanverdi, İlhan, Şahin, Yavuz, Sağlam, Beyhan, Karateke, Ateş
Foilsithe in 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

le Ozkars, Mehmet Yasar, Keskın, Ozlem, Bayram, Nazan, Onay, Huseyin, Keskın, Mehmet, Bayram, Hasan, Sahın, Yavuz, Küçükosmanoğlu, Ercan, Kırık, Serkan
Foilsithe in Postepy Dermatol Alergol (2019)

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

le 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.
Foilsithe in Eur J Hum Genet (2020)

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

le 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.
Foilsithe in Am J Hum Genet (2019)