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1

Sodium phenylbutyrate in Huntington's disease: A dose-finding study

Penelope Hogarth, Luca Lovrecic, Dimitri Krainc

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 57 KB

english, 2007

2

Interstitial deletion 2p11.2–p12: Further delineation

Karin Writzl, Luca Lovrečić, Borut Peterlin

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 125 KB

english, 2009

3

Gene expression changes in blood as a putative biomarker for Huntington's disease

Luca Lovrecic, Andrej Kastrin, Jan Kobal, Zvezdan Pirtosek, Dimitri Krainc, Borut Peterlin

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 176 KB

english, 2009

4

Human Y-specific STR haplotypes in the Western Croatian population sample

Luca Lovrečić, Smiljana Ristić, Bojana Brajenović, Miljenko Kapović, Borut Peterlin

Journal:

Forensic Science International

Year:

2005

Language:

english

File:

PDF, 76 KB

english, 2005

5

SATB2haploinsufficiency in patients with cleft palate

Karin Writzl, Luca Lovrečić, Ján Vojtaššák, Borut Peterlin, Eurocran Gene-Environment Interaction Group

Journal:

Central European Journal of Medicine

Year:

2010

Language:

english

File:

PDF, 1.21 MB

english, 2010

6

A new case of rare proximal 3q13 interstitial deletion

Luca Lovrecic, Gorazd Rudolf, Alenka Veble, Borut Peterlin

Journal:

Central European Journal of Medicine

Year:

2011

Language:

english

File:

PDF, 390 KB

english, 2011

7

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

Smiljana Ristić, Luca Lovrečić, Bojana Brajenović-Milić, Nada Starčević-Čizmarević, Saša Šega Jazbec, Juraj Sepčić, Miljenko Kapović, Borut Peterlin

Journal:

Neuroscience Letters

Year:

2005

Language:

english

File:

PDF, 67 KB

english, 2005

8

Angiotensin-Converting Enzyme Gene Polymorphism in Patients with Multiple Sclerosis from Bosnia and Herzegovina

Klupka-Sarić, Inge, Peterlin, Borut, Lovrečić, Luca, Sinanović, Osman, Vidović, Mirjana, Šehanović, Aida, Čizmarević, Nada Starčević, Sepčić, Juraj, Kapović, Miljenko, Ristić, Smiljana

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2011

Language:

english

File:

PDF, 97 KB

english, 2011

9

Specific gene expression differences in cumulus cells as potential biomarkers of pregnancy

Burnik Papler, Tanja, Vrtačnik Bokal, Eda, Maver, Aleš, Lovrečić, Luca

Journal:

Reproductive BioMedicine Online

Year:

2015

Language:

english

File:

PDF, 571 KB

english, 2015

10

No Specific Gene Expression Signature in Human Granulosa and Cumulus Cells for Prediction of Oocyte Fertilisation and Embryo Implantation

Burnik Papler, Tanja, Vrtacnik Bokal, Eda, Lovrecic, Luca, Kopitar, Andreja Natasa, Maver, Ales, Gleicher, Norbert

Journal:

Year:

2015

Language:

english

File:

PDF, 1.68 MB

english, 2015

11

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

Vrecar, Irena, Peterlin, Borut, Teran, Natasa, Lovrecic, Luca

Journal:

Biochemia Medica

Year:

2015

Language:

english

File:

PDF, 125 KB

english, 2015

12

The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis

Živković, Maja, Starčević Čizmarević, Nada, Lovrečić, Luca, Klupka-Sarić, Inge, Stanković, Aleksandra, Gašparović, Iva, Lavtar, Polona, Dinčić, Evica, Stojković, Ljiljana, Rudolf, Gorazd, Šega Jazbec,

Journal:

Disease Markers

Year:

2014

Language:

english

File:

PDF, 257 KB

english, 2014

13

No association of CCR5Δ32 gene mutation with multiple sclerosis in Croatian and Slovenian patients

Ristić, Smiljana, Lovrečić, Luca, Starčević-Čizmarevič, Nada, Brajenović-Milić, Bojana, Jazbec, Saša Šega, Barac-Latas, Vesna, Vejnović, Danilo, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut

Journal:

Multiple Sclerosis Journal

Year:

2006

Language:

english

File:

PDF, 171 KB

english, 2006

14

MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Gašparović, Iva, Čizmarević, Nada Starčević, Lovrečić, Luca, Perković, Olivio, Lavtar, Polona, Sepčić, Juraj, Jazbec, Saša Šega, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana

Journal:

Journal of Neuroimmunology

Year:

2015

Language:

english

File:

PDF, 187 KB

english, 2015

15

Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation

Ales, Maver, Luca, Lovrecic, Marija, Volk, Gorazd, Rudolf, Karin, Writzl, Ana, Blatnik, Alenka, Hodzic, Peterlin, Borut

Journal:

Genetics in Medicine

Year:

2016

Language:

english

File:

PDF, 2.14 MB

english, 2016

16

A New Case of an Extremely Rare 3p21.31 Interstitial Deletion

Lovrecic, Luca, Bertok, Sara, Žerjav Tanšek, Mojca

Journal:

Molecular Syndromology

Year:

2016

Language:

english

File:

PDF, 329 KB

english, 2016

17

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

Vrečar, Irena, Rudolf, Gorazd, Peterlin, Borut, Lovrecic, Luca

Journal:

Molecular Cytogenetics

Year:

2015

Language:

english

File:

PDF, 643 KB

english, 2015

18

Nutriepigenomics

Remely, Marlene, Stefanska, Barbara, Lovrecic, Luca, Magnet, Ulrich, Haslberger, Alexander G.

Journal:

Current Opinion in Clinical Nutrition & Metabolic Care

Year:

2015

Language:

english

File:

PDF, 210 KB

english, 2015

19

11q terminal deletion and combined immunodeficiency (Jacobsen syndrome): Case report and literature review on immunodeficiency in Jacobsen syndrome

Blazina, Štefan, Ihan, Alojz, Lovrečić, Luca, Hovnik, Tinka

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 84 KB

english, 2016

20

Clinical utility of array comparative genomic hybridisation in prenatal setting

Lovrecic, Luca, Remec, Ziga Iztok, Volk, Marija, Rudolf, Gorazd, Writzl, Karin, Peterlin, Borut

Journal:

BMC Medical Genetics

Year:

2016

Language:

english

File:

PDF, 481 KB

english, 2016

21

Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-β treatment response in multiple sclerosis patients

Ristić, Smiljana, Starčević Čizmarević, Nada, Lavtar, Polona, Lovrečić, Luca, Perković, Olivio, Sepčić, Juraj, Šega Jazbec, Saša, Kapović, Miljenko, Peterlin, Borut

Journal:

Pharmacogenetics and Genomics

Year:

2017

Language:

english

File:

PDF, 121 KB

english, 2017

22

Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases

Bergant, Gaber, Maver, Ales, Lovrecic, Luca, Čuturilo, Goran, Hodzic, Alenka, Peterlin, Borut

Journal:

Genetics in Medicine

Year:

2017

Language:

english

File:

PDF, 493 KB

english, 2017

23

Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21

Volk, Marija, Maver, Aleš, Hodžić, Alenka, Lovrečić, Luca, Peterlin, Borut

Journal:

Omics A Journal of Integrative Biology

Year:

2017

Language:

english

File:

PDF, 161 KB

english, 2017

24

Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping

Lovrečić, Luca, Rajar, Polona, Volk, Marija, Bertok, Sara, Gnidovec Stražišar, Barbara, Osredkar, Damjan, Jekovec Vrhovšek, Maja, Peterlin, Borut

Journal:

Journal of Applied Genetics

Year:

2018

Language:

english

File:

PDF, 493 KB

english, 2018

25

Transcriptomic Analysis and Meta-Analysis of Human Granulosa and Cumulus Cells

Burnik Papler, Tanja, Vrtacnik Bokal, Eda, Maver, Ales, Kopitar, Andreja Natasa, Lovrečić, Luca, Feltus, Frank Alexander

Journal:

Year:

2015

Language:

english

File:

PDF, 1.69 MB

english, 2015

26

Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability

Lovrecic, Luca, Gnan, Chiara, Baldan, Federica, Franzoni, Alessandra, Bertok, Sara, Damante, Giuseppe, Isidor, Bertrand, Peterlin, Borut

Journal:

Molecular Cytogenetics

Year:

2018

Language:

english

File:

PDF, 1.01 MB

english, 2018

27

The frequency of CNV s in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy

Rudolf, Gorazd, Lovrečić, Luca, Tul, Nataša, Teran, Nataša, Peterlin, Borut

Journal:

Molecular Genetics & Genomic Medicine

Year:

2019

Language:

english

File:

PDF, 380 KB

english, 2019

28

The frequency of CNV s in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy

Rudolf, Gorazd, Lovrečić, Luca, Tul, Nataša, Teran, Nataša, Peterlin, Borut

Journal:

Molecular Genetics & Genomic Medicine

Year:

2019

File:

PDF, 380 KB

2019

29

Combination of QF‐PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage

Lovrečić, Luca, Pereza, Nina, Jaklič, Helena, Ostojić, Saša, Peterlin, Borut

Journal:

Molecular Genetics & Genomic Medicine

Year:

2019

File:

PDF, 449 KB

2019

30

Chronic Lymphocytic Leukemia with Divergent Richterâs Transformation into a Clonally Related Classical Hodgkinâs and Plasmablastic Lymphoma: A Case Report

Gasljevic, Gorana, Grat, Mateja, Kloboves Prevodnik, Veronika, Grcar Kuzmanov, Biljana, Gazic, Barbara, Lovrecic, Luca, Podgornik, Helena

Journal:

Case Reports in Oncology

Year:

2020

File:

PDF, 2.08 MB

2020

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