Get started
Author

Hakan Ulucan

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
2015 · Ender Karaca, Tamar Harel, et al. · Neuron · 316
PDF
Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes
2015 · Bo Yuan, Davut Pehlivan, et al. · Journal of Clinical Investigation · 161
PDF
Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type
2015 · Mala Isrie, Martin Breuss, et al. · The American Journal of Human Genetics · 87
PDF
Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVCgene
2008 · Hakan Ulucan, Davut Gül, et al. · BMC Medical Genetics · 32
PDF
Incomplete Currarino triad as an embryological variant
2006 · Mehmet Turgut, Emre Çullu, et al. · Journal of Neurosurgery Pediatrics · 22
Poikiloderma with neutropenia: Genotype‐ethnic origin correlation, expanding phenotype and literature review
2014 · Asuman Koparir, Alper Gezdirici, et al. · American Journal of Medical Genetics Part A · 20
Circumferential skin folds and multiple anomalies
2013 · Hakan Ulucan, Erkan Koparir, et al. · Clinical Dysmorphology · 15
A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve–Melchior–Clausen syndrome
2013 · Mehmet Seven, Erkan Koparir, et al. · Clinical Dysmorphology · 10
A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 ( NF1 ) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features
2003 · Cagatay Oktenli, Mutlu Saglam, et al. · Clinical Dysmorphology · 10
Preliminary study on DNA damage in non breast‐fed infants
2002 · RuŞen DÜndaröz, Halil İBrahim Aydin, et al. · Pediatrics International · 7
PDF
Whole-exome sequencing revealed two novel mutations in Usher syndrome
2015 · Asuman Koparir, Omer Faruk Karatas, et al. · Gene · 6
A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication
2013 · Mehmet Seven, Alper Gezdirici, et al. · Gene · 5
Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G
2004 · Vedat Köseoglu, Erol Kismet, et al. · Pediatrics International · 5
Analysis of DNA Damage Using the Comet Assay in Infants Fed Cow’s Milk
2003 · Ruşen Dündaröz, Hakan Ulucan, et al. · Neonatology · 5
A novel mutation in FK506 binding protein-like (FKBPL) causes male infertility
2021 · Derya Akyuz Sengun, Esra Guzel Tanoglu, et al. · Croatian Medical Journal · 4
PDF
Acrocallosal syndrome: report of five Turkish patients
2004 · Davut G??l, Hakan Ulucan, et al. · Clinical Dysmorphology · 4
Evaluation of DNA damage using the comet assay in children on long‐term benzathine penicillin for secondary prophylaxis of rheumatic fever
2001 · Ruşen Dündaröz, Hakan Ulucan, et al. · Pediatrics International · 4
PDF
De novo pericentric inversion of chromosome 5 in a girl with mental retardation and unilateral ear malformation
2006 · Hakan Ulucan, Rıdvan Akın, et al. · American Journal of Medical Genetics Part A · 3
A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia
2012 · Alper Gezdirici, Alper Yenigun, et al. · Clinical Dysmorphology · 2
Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?
2001 · ??agatay ??ktenli, Hakan Ulucan, et al. · Clinical Dysmorphology · 2
Familial sick sinus syndrome
2013 · Osman Sonmez, Ahmet Bacaksiz, et al. · The Anatolian Journal of Cardiology · 1
Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?
2003 · ??a??atay ??ktenli, Hakan Ulucan, et al. · Clinical Dysmorphology · 1
Unilateral split foot, torticollis, congenital heart defect and hydrocephaly: a new syndrome?
2002 · Davut G??l, B??lent ??nay, et al. · Clinical Dysmorphology · 1
A rare case of Happle-Tinschert syndrome
2016 · Seven Mehmet, Emre Kırat, et al. · 日本人類遺伝学会大会プログラム・抄録集
染色体8q上の欠損と染色体2と4間の均衡した相互の転座をもつランガーギデオン症候群 | 文献情報 | J-GLOBAL 科学技術総合リンクセンター
2016 · Emre Kırat, Koparir Asuman, et al. · 日本人類遺伝学会大会プログラム・抄録集
Works count: 31
Citation count: 723
H-index: 9
I10-index: 9
Year
Topic
Type