Nilufer Sahin-Calapoglu

Genetic Study of Demyelinating form of Autosomal-Recessive Charcot–Marie–Tooth Diseases in a Turkish Family

M. Calapoğlu, Nilufer Sahin-Calapoglu, M. Soyoz, 2009, The International journal of neuroscience.

Novel GDAP1 Mutation in a Turkish Family with CMT2K (CMT2K with Novel GDAP1 Mutation)

M. Tan, M. Calapoğlu, Nilufer Sahin-Calapoglu, 2009, NeuroMolecular Medicine.

A Case-Control Association Study of RANTES (-28C>G) Polymorphism as a Risk Factor for Parkinson's Disease in Isparta, Turkey

M. Calapoğlu, S. Demirci, Nilufer Sahin-Calapoglu, 2016, Parkinson's disease.

A novel TMPRSS 3 missense mutation in a DFNB 8 / 10 family prevents proteolytic activation of the protein WATTENHOFER

A. Reymond, S. Antonarakis, B. Rossier, 2018 .

A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein

A. Reymond, S. Antonarakis, B. Rossier, 2005, Human Genetics.

Serotonin Transporter Bi- and Triallelic Genotypes and Their Relationship with Anxiety and Academic Performance: A Preliminary Study

M. Calapoğlu, Ataman Karaçöp, M. Soyöz, 2010, Neuropsychobiology.