A. Hodzic

发表

Vaginal Microbiome Signature Is Associated With Spontaneous Preterm Delivery

B. Peterlin, A. Maver, A. Haslberger, 2019, Front. Med..

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

B. Peterlin, A. Maver, A. Hodzic, 2017, Omics : a journal of integrative biology.

A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion

B. Peterlin, A. Hodzic, N. Pereza, 2017, American journal of reproductive immunology.

Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion

B. Peterlin, A. Maver, A. Hodzic, 2016, Croatian medical journal.

Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism

N. Drouot, M. Baulac, M. Habert, 2020, Movement disorders : official journal of the Movement Disorder Society.

Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice

B Peterlin, B. Peterlin, A. Maver, 2018, Clinical genetics.

De novo mutations in idiopathic male infertility—A pilot study

T. Kunej, B. Peterlin, P. Noveski, 2020, Andrology.

Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility

B. Peterlin, D. Plaseska-Karanfilska, A. Maver, 2017, Andrology.

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

Gorazd Rudolf, Ales Maver, B. Peterlin, 2016, Genetics in Medicine.

The Role of Next Generation Sequencing in the Differential Diagnosis of Caroli’s Syndrome

B. Peterlin, A. Hodzic, G. Bergant, 2018, Balkan Journal of Medical Genetics : BJMG.

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

B. Peterlin, A. Maver, A. Hodzic, 2017, Genetics in Medicine.

The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

B. Peterlin, A. Hodzic, S. Ristić, 2016, Brain and behavior.

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

B. Peterlin, A. Maver, A. Hodzic, 2018, PloS one.

Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility

B. Peterlin, A. Maver, C. Tulić, 2013, PloS one.

The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion

B. Peterlin, A. Hodzic, N. Pereza, 2015, Journal of Assisted Reproduction and Genetics.

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder

B. Peterlin, A. Maver, A. Hodzic, 2023, Frontiers in genetics.

Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss

B. Peterlin, A. Hodzic, N. Pereza, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion

B. Peterlin, J. Dotlic, A. Hodzic, 2018, PloS one.

Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion

B. Peterlin, A. Hodzic, N. Pereza, 2017, Journal of Assisted Reproduction and Genetics.

A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans–A cohort study

A. Maver, A. Hodzic, K. Writzl, 2023, PloS one.