Irena Vrecar

Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislation

B. Peterlin, L. Lovrečić, N. Teran, 2015, Biochemia medica.

PEDIA: prioritization of exome data by image analysis

Borut Peterlin, Sebastian Köhler, Na Zhu, 2018, Genetics in Medicine.

Molecular karyotyping – a new approach in clinical and laboratory genetics

B. Peterlin, L. Lovrečić, Irena Vrecar, 2014 .

Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Absent Speech, and Involuntary Movements

Sofia Douzgou, Jill Clayton-Smith, W. Reardon, 2017, Journal of Pediatric Genetics.

Family history based approach in risk prediction for Parkinson's disease: Additional contribution of familial associated disorders

D. Georgiev, B. Peterlin, Z. Pirtošek, 2015 .

Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss

B. Peterlin, L. Lovrečić, G. Rudolf, 2015, Molecular Cytogenetics.

Content validity and inter-rater reliability of the Halliwick-concept-based instrument ‘Swimming with Independent Measure’

G. Vidmar, Irena Vrecar, K. Sršen, 2012, International journal of rehabilitation research. Internationale Zeitschrift fur Rehabilitationsforschung. Revue internationale de recherches de readaptation.

Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service

Borut Peterlin, Dimitar Hristovski, Irena Vrecar, 2017, Journal of Medical Systems.

PEDIA: prioritization of exome data by image analysis

M. Nöthen, O. Bar, S. Köhler, 2018, Genetics in Medicine.