Y. Sahin

发表

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

P. Kumru, T. Kutlu, B. Devranoğlu, 2017, Turkish journal of obstetrics and gynecology.

Celiac disease in Williams-Beuren syndrome.

U. Arslan, H. Ozen, P. Simsek-Kiper, 2014, The Turkish journal of pediatrics.

The genetic counseling in a patient affected by choroideremia solved with the whole-exome sequencing approach

Erik Burton, Y. Sahin, Bedia Sahin, 2022, Indian journal of ophthalmology.

Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability

J. Lupski, R. Gibbs, S. Jhangiani, 2022, HGG advances.

Area under curve of temporal estradiol measurements for prediction of the detrimental effect of estrogen exposure on implantation

T. Kutlu, B. Devranoğlu, A. Karateke, 2016, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Serum substance P concentrations to predict oocyte maturation index and clinical pregnancy

T. Kutlu, A. Karateke, I. Sanverdi, 2017, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Regenerative Endodontic Procedures in Necrotic Mature Teeth with Periapical Radiolucencies: A Preliminary Randomized Clinical Study.

H. Arslan, H. Ahmed, E. Doğanay Yıldız, 2019, Journal of endodontics.

Partial monosomy 3q26.33-3q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case report

T. Liehr, Y. Alanay, G. Utine, 2014, Clinical dysmorphology.

Does the Modification of Starting Gonadotropin Dose During Intracytoplasmic Sperm Injection Cycle Have Any Significant Impact on Cycle Outcome?

T. Kutlu, Semra Kayataş Eser, I. Sanverdi, 2017 .

Orientation of some Heterorhabditis bacteriophora (Poinar, 1976) (Rhabditida: Heterorhabditidae) strains to Lolium perenne L. (Poales: Poaceae) and Galleria mellonella (L., 1758) (Lepidoptera: Pyralidae)

S. Yıldırım, Y. Sahin, A. Susurluk, 2019, Turkish Journal of Entomology.

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

Y. Sahin, Ayşegül Özcan, 2017, Journal of Pediatric Genetics.

Effects of Chromosomal Translocations on Sperm Count in Azoospermic and Oligospermic Cases

A. Gezdirici, S. Yalçıntepe, Akif Ayaz, 2022, Journal of Basic and Clinical Health Sciences.

Relation between birth weight and thyroid function in preeclampsia-eclampsia.

Y. Sahin, H. Paşaoğlu, Z. Ozkececi, 1994, Gynecologic and obstetric investigation.

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

J. Lupski, R. Gibbs, E. Boerwinkle, 2019, American journal of human genetics.

MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia

Michael F. Wangler, J. Lupski, D. Krainc, 2021, Annals of neurology.

A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease

P. Striano, S. Bianca, J. Goraya, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

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?

T. Kutlu, A. Karateke, I. Sanverdi, 2016, Turkish journal of obstetrics and gynecology.

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

H. Bayram, H. Onay, M. Keskin, 2019, Postepy dermatologii i alergologii.

Structural and Genomic Variation in Preterm Birth

J. Padbury, E. Feingold, K. Ryckman, 2016, Pediatric Research.

A hereditary angioedema screening on an index case: Turkey.

H. Bayram, M. Keskin, O. Keskin, 2018, Asian Pacific journal of allergy and immunology.

The Control of Turkestan Cockroach Blatta lateralis (Dictyoptera: Blattidae) by The Entomopathogenic nematode Heterorhabditis bacteriophora HBH (Rhabditida: Heterorhabditidae) Using Hydrophilic Fabric Trap

I. A. Susurluk, Y. Sahin, 2020 .

1 p 36 Microdeletion Syndrome : A Case Report

P. Akkus, E. Utine, K. Boduroğlu, 2014 .

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

Johnathon R. Walls, Marc S. Williams, J. Lupski, 2020, European Journal of Human Genetics.

The TWIST2 mutation causes Setleis syndrome: a rare clinical case report

A. Ozer, U. Celik, S. Yalçıntepe, 2017, Clinical dysmorphology.

Control potentials of some entomopathogenic nematodes against Asian chestnut gall wasp, Dryocosmus kuriphilus Yasumatsu, 1951 (Hymenoptera: Cynipidae)

N. S. Gençer, Y. Sahin, A. Susurluk, 2020, Turkish Journal of Entomology.

A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis

Gülay Güngör, O. Güngör, S. Ceylaner, 2017, Brain and Development.

DiGeorge Syndrome Associated with Azoospermia: First case in the literature.

Y. Sahin, Ayşegül Özcan, 2017, Turkish journal of urology.

Interstitial deletion 5p14.1‐p15.2 and 5q14.3‐q23.2 in a patient with clubfoot, blepharophimosis, arthrogryposis, and multiple congenital abnormalities

M. Erdoğan, B. Balta, Y. Sahin, 2017, American journal of medical genetics. Part A.

Novel homozygous AP3B2 mutations in four individuals with developmental and epileptic encephalopathy: A rare clinical entity

C. Dilber, Y. Sahin, Gülen Yücel, 2022, Clinical Neurology and Neurosurgery.

Histologic Evaluation of Regenerated Tissues in the Pulp Spaces of Teeth with Mature Roots at the Time of the Regenerative Endodontic Procedures.

H. Arslan, H. Topçuoğlu, B. Gündoğdu, 2019, Journal of endodontics.

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

T. Kutlu, A. Karateke, I. Sanverdi, 2016, Turkish journal of obstetrics and gynecology.

Eighth case of Li‐Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype

H. Kaymakçalan, Saeed Farajzadeh Valilou, Y. Sahin, 2023, American journal of medical genetics. Part A.

A compound heterozygous EARS2 mutation associated with mild leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL)

Gülay Güngör, O. Güngör, C. Dilber, 2016, Brain and Development.

Arrhythmia in thiamine responsive megaloblastic anemia syndrome.

N. Narin, S. Kurtoğlu, A. Baykan, 2018, The Turkish journal of pediatrics.

Seroreactivity against retinal proteins in a case of POC1B gene associated cone dystrophy with normal funduscopic appearance: a systematic approach to diagnosis

S. Demirel, Ö. Yanık, F. Batıoğlu, 2022, Ophthalmic genetics.

Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy

Hüseyin Demirci, Gülay Güngör, O. Güngör, 2017, Acta Neurologica Belgica.

A case with congenital disorder of glycosylation with defective fucosylation 2 and new mutation in FUK gene

Y. Sahin, N. Özgün, 2021, Brain and Development.

The Predictive Value of the Pentraxin 3 Concentration in Cumulus Cell Culture Media for the Embryo Implantation

T. Irez, O. Guralp, E. Malik, 2021, Gynecology Obstetrics & Reproductive Medicine.

A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis

Gülay Güngör, O. Güngör, S. Ceylaner, 2017, Brain and Development.