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G. Rudolf · SciRah

Researcher profile · Semantic Scholar

G. Rudolf

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G. Rudolf — researcher profile on SciRah

h-index: 13
Works: 35
Citations: 985

Most-cited papers

Medication use in pregnancy: a cross-sectional, multinational web-based study
A. Lupattelli, O. Spigset, M. Twigg, K. Zagorodnikova +14 more
2014BMJ Open427 citations Open access
Semantic Scholar
PEDIA: prioritization of exome data by image analysis
Tzung-Chien Hsieh, M. Mensah, J. Pantel, D. Aguilar +90 more
2018Genetics in Medicine83 citations Open access
Semantic Scholar
Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
A. Maver, Polona Lavtar, S. Ristić, S. Stopinšek +15 more
2017Scientific Reports61 citations Open access
Semantic Scholar
PATTERNS AND FACTORS ASSOCIATED WITH LOW ADHERENCE TO PSYCHOTROPIC MEDICATIONS DURING PREGNANCY—A CROSS‐SECTIONAL, MULTINATIONAL WEB‐BASED STUDY
A. Lupattelli, O. Spigset, I. Björnsdottir, K. Hämeen-Anttila +14 more
2015Depression and Anxiety61 citations Open access
Semantic Scholar
Novel mutations including deletions of the entire OFD1 gene in 30 families with type I orofaciodigital syndrome: a study of the extensive clinical variability
I. J. Bisschoff, C. Zeschnigk, D. Horn, B. Wellek +26 more
2012Human Mutation53 citations Open access
Semantic Scholar
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis
Polona Lavtar, G. Rudolf, A. Maver, A. Hodzic +12 more
2018PLoS ONE50 citations Open access
Semantic Scholar
Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism
T. Wirth, L. Mariani, G. Bergant, M. Baulac +11 more
2020Movement Disorders37 citations
Semantic Scholar
Self-reported perinatal depressive symptoms and postnatal symptom severity after treatment with antidepressants in pregnancy: a cross-sectional study across 12 European countries using the Edinburgh Postnatal Depression Scale
A. Lupattelli, M. Twigg, K. Zagorodnikova, M. Moretti +9 more
2018Clinical Epidemiology33 citations Open access
Semantic Scholar
Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's disease.
Thomas Wirth, S. Weibel, S. Montaut, K. Bigaut +4 more
2017Parkinsonism & Related Disorders28 citations
Semantic Scholar
Clinical utility of array comparative genomic hybridisation in prenatal setting
L. Lovrečić, Ž. I. Remec, M. Volk, G. Rudolf +2 more
2016BMC Medical Genetics25 citations Open access
Semantic Scholar
The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis
M. Živković, N. Starčević Čizmarević, L. Lovrečić, Inge Klupka-Sarić +13 more
2014Disease Markers18 citations Open access
Semantic Scholar
Clinical Exome Sequencing as a Novel Tool for Diagnosing Loeys-Dietz Syndrome Type 3.
A. Blinc, A. Maver, G. Rudolf, J. Tasic +3 more
2015European Journal of Vascular and Endovascular Surgery16 citations Open access
Semantic Scholar
C.35delG/ GJB2 and del(GJB6-D13S1830) mutations in Croatians with prelingual non-syndromic hearing impairment
I. Medica, G. Rudolf, Manuela Balaban, B. Peterlin
2005BMC Ear, Nose and Throat Disorders13 citations Open access
Semantic Scholar
Incidence of the del35G/GJB2 mutation in Croatian newborns with hearing impairment.
I. Medica, G. Rudolf, I. Prpić, M. Stanojevic +1 more
2005Medical Science Monitor11 citations
Semantic Scholar
Impact of prenatal screening on the prevalence of Down syndrome in Slovenia
G. Rudolf, N. Tul, I. Verdenik, M. Volk +6 more
2017PLoS ONE10 citations Open access
Semantic Scholar
Poster I
J. Chanson, Giulia Pacini, N. Collongues, G. Rudolf +4 more
20129 citations
Semantic Scholar
CTLA‐4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients
N. S. Čizmarević, I. Gašparović, B. Peterlin, J. Sepčić +4 more
2011International Journal of Immunogenetics9 citations
Semantic Scholar
Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
A. Maver, Polona Lavtar, S. Ristić, S. Stopinšek +15 more
2017Scientific Reports7 citations Open access
Semantic Scholar
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss
Irena Vrecar, G. Rudolf, B. Peterlin, L. Lovrečić
2015Molecular Cytogenetics7 citations Open access
Semantic Scholar
Connexin 26 (GJB2) and connexin 30 del(GJB6-D13S1830) mutations in Slovenians with prelingual non-syndromic deafness
Saba Battellino, G. Rudolf, M. Žargi, K. T. Podkrajšek +1 more
20116 citations
Semantic Scholar
Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy
Anja Kovanda, L. Lovrečić, G. Rudolf, Ivana Babic Bozovic +3 more
2023medRxiv5 citations Open access
Semantic Scholar
DNA testiranje u medicini
G. Rudolf, B. Peterlin
20094 citations
Semantic Scholar
The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy
G. Rudolf, L. Lovrečić, N. Tul, N. Teran +1 more
2019Molecular Genetics & Genomic Medicine3 citations Open access
Semantic Scholar
GJB 2 and GJB 6 mutations in Croatians with prelingual non-syndromic hearing impairment
I. Medica, G. Rudolf, Manuela Balaban, B. Peterlin
20053 citations
Semantic Scholar
A new case of rare proximal 3q13 interstitial deletion
L. Lovrečić, G. Rudolf, A. Veble, B. Peterlin
20112 citations Open access
Semantic Scholar
Genomic Testing for Prenatal Clinical Evaluation of Congenital Anomalies
G. Rudolf, L. Lovrečić, A. Maver, M. Volk +1 more
20181 citations Open access
Semantic Scholar
Medicinska genetika u kliničkoj obradi raka dojke
G. Rudolf, Borut Peterlin
20101 citations
Semantic Scholar
UPORABA DNK GENETSKEGA TESTA V MEDICINI PRACTICAL CONSIDERATIONS OF DNA TESTING IN MEDICINE
G. Rudolf, B. Peterlin
20091 citations
Semantic Scholar
NEURODEGENERATION UPDATES AND THE 30 YEARS OF AMYLOID CASCADE HYPOTHESIS
M. Hero, B. Petek, G. Bergant, A. Maver +3 more
20220 citations
Semantic Scholar
The association between antidepressant treatment in pregnancy and self-report of postnatal depressive symptoms using the Edinburgh Postnatal Depression Scale
A. Lupattelli, M. Twigg, K. Zagorodnikova, M. Moretti +9 more
2018Reproductive Toxicology0 citations
Semantic Scholar
Association of circadian rhythm genes ARNTL and CLOCK with multiple sclerosis (MS).
Polona Lavtar, G. Rudolf, A. Maver, L. Lovrečić +11 more
20130 citations
Semantic Scholar
Angiotensin-converting enzyme (ACE) I/D gene polymorphism in multiple sclerosis
A. Stanković, I. Gašparović, B. Peterlin, Inge Klupka-Sarić +12 more
20110 citations
Semantic Scholar
Clinical genetics and breast cancer
G. Rudolf, B. Peterlin
20100 citations
Semantic Scholar
DNA testing in medicine
G. Rudolf, B. Peterlin
20090 citations
Semantic Scholar
Practical considerations of DNA testing in medicine.
G. Rudolf, B. Peterlin
20090 citations
Semantic Scholar

Frequent co-authors

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B. Peterlin×25
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B. Peterlin — researcher profile on SciRah
L. Lovrečić×10
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L. Lovrečić — researcher profile on SciRah
Polona Lavtar×7
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Polona Lavtar — researcher profile on SciRah
S. Ristić×7
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A. Maver — researcher profile on SciRah

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J. Sepčić — researcher profile on SciRah

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A. Lupattelli×4

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