Get started
Author

Goražd Rudolf

Observed names: G Rudolf, G. De M. Rudolf, G. Rudolf, G. d. M. Rudolf, G. de M. Rudolf, G.DE.M. Rudolf, Gorazd Rudolf, Rudolf, Gorazd
Observed institutions: University of Ljubljana, Ljubljana University Medical Centre, Institut de génétique et de biologie moléculaire et cellulaire, Hôpitaux Universitaires de Strasbourg, Hôpital d'Hautepierre, Université de Strasbourg
ORCID: 0000-0003-3863-3308
Observed ORCID: 0000-0003-3863-3308
OpenAlex ID: A5102816628
Medication use in pregnancy: a cross-sectional, multinational web-based study
2014 · A Lupattelli, O Spigset, et al. · BMJ Open · 526
PDF
PEDIA: prioritization of exome data by image analysis
2019 · Tzung-Chien Hsieh, Martin A. Mensah, et al. · Genetics in Medicine · 84
PDF
Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
2017 · Ales Maver, Polona Lavtar, et al. · Scientific Reports · 68
PDF
Patterns and Factors Associated With Low Adherence to Psychotropic Medications During Pregnancy-a Cross-sectional, Multinational Web-based Study
2015 · Angela Lupattelli, Olav Spigset, et al. · Depression and Anxiety · 67
Novel Mutations Including Deletions of the EntireOFD1Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability
2012 · Izak J. Bisschoff, Christine Zeschnigk, et al. · Human Mutation · 55
PDF
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis
2018 · Polona Lavtar, Gorazd Rudolf, et al. · PLoS ONE · 54
Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism
2020 · Thomas Wirth, Louise Laure Mariani, et al. · Movement Disorders · 41
Clinical utility of array comparative genomic hybridisation in prenatal setting
2016 · Luca Lovrecic, Ziga Iztok Remec, et al. · BMC Medical Genetics · 26
PDF
The Treatment of Depression with Desoxyephedrine (Methedrine)
1949 · G. de M. Rudolf · Journal of Mental Science · 23
Institute of Neurology
1966 · G. de M. Rudolf · BMJ · 22
PDF
The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis
2014 · Maja Živković, Nada Starčević Čizmarević, et al. · Disease Markers · 17
PDF
Clinical Exome Sequencing as a Novel Tool for Diagnosing Loeys-Dietz Syndrome Type 3
2015 · A. Blinc, A. Maver, et al. · European Journal of Vascular and Endovascular Surgery · 16
C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment
2005 · Igor Medica, Gorazd Rudolf, et al. · BMC Ear Nose and Throat Disorders · 12
PDF
Impact of prenatal screening on the prevalence of Down syndrome in Slovenia
2017 · Gorazd Rudolf, Nataša Tul, et al. · PLoS ONE · 11
PDF
Incidence of the del35G/GJB2 mutation in Croatian newborns with hearing impairment.
2005 · Igor Medica, Gorazd Rudolf, et al. · PubMed · 11
CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients
2011 · N. Starčević Čizmarević, I. Gašparović, et al. · International Journal of Immunogenetics · 9
Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy
2023 · Anja Kovanda, Luca Lovrečić, et al. · Genes · 6
PDF
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss
2015 · Irena Vrečar, Gorazd Rudolf, et al. · Molecular Cytogenetics · 6
PDF
The Treatment of Mental Defectives with Thiamine
1949 · G. de M. Rudolf · Journal of Mental Science · 5
DNA testing in medicine
2009 · Goražd Rudolf, Borut Peterlin · Bioline International (Bioline International) · 4
PDF
The frequency of CNV s in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy
2019 · Gorazd Rudolf, Luca Lovrečić, et al. · Molecular Genetics & Genomic Medicine · 3
PDF
A new case of rare proximal 3q13 interstitial deletion
2011 · Luca Lovrecic, Gorazd Rudolf, et al. · Open Medicine · 3
PDF
Improvement in Mental Defectives in Colonies
1950 · G. De M. Rudolf · Journal of Mental Science · 3
Duration of Sleep
1968 · G. de M. Rudolf · BMJ · 2
Genomic Testing for Prenatal Clinical Evaluation of Congenital Anomalies
2018 · Gorazd Rudolf, Luca Lovrečić, et al. · InTech eBooks · 1
PDF
Works count: 44
Citation count: 1,083
H-index: 12
I10-index: 15
Year
Topic
Type