Epigenetic signature of chronic maternal stress load during pregnancy might be a potential biomarker for spontaneous preterm birth by Rogac M, Peterlin B

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A systematic clinical review of prenatally diagnosed tetrasomy 9p by Vinkšel M, Volk M, Peterlin B, Lovrecic L

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Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and... by Maver A, Čuturilo G, Ruml Stojanović J, Peterlin B

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The role of next generation sequencing in the differential diagnosis of caroli’s syndrome by Smolović B, Muhović D, Hodžić A, Bergant G, Peterlin B

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Study of Three Single Nucleotide Polymorphisms in the Slc6a14 Gene in Association with Male Infertility by Noveski P., Mircevska M., Plaseski T., Peterlin B., Plaseska-Karanfilska D.

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Family history as an important factor for stratifying participants in genetic studies of major depression by Zalar B, Blatnik A, Maver A, Klemenc-Ketiš Z, Peterlin B

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P-TEFb is not an essential elongation factor for the intronless human U2 snRNA and histone H2b genes. by Medlin, J, Scurry, A, Taylor, A, Zhang, F, Peterlin, B, Murphy, S

Polymorphism of the ADRB2 rs1042713 gene is not associated with spontaneous preterm birth: Analyses in a Slovenian sample and meta analysis by Peterlin A, Maver A, Jan Z, Lovrecic L, Tul N, Peterlin B

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A novel likely pathogenic variant in the RUNX1 gene as the cause of congenital thrombocytopenia by Despotović M, Pereza N, Peterlin B, Ostojić S, Golob B, Maver A, Roganović J

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A novel variant in the LIPA gene associated with distinct phenotype by Sarajlija A., Armengol L., Maver A., Kitic I., Prokic D., Cehic M., Djuricic M.S., Peterlin B.

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Interactions between Nef and AIP1 proliferate multivesicular bodies and facilitate egress of HIV-1 by Plemenitas Ana, Tanuri Amilcar, Aguiar Renato S, Lopes Adriana, Chen Nan, Costa Luciana J, Peterlin B Matija

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Otopalatodigital syndrome type I: novel characteristics and prenatal manifestations in two siblings by Joksic I, Cuturilo G, Jurisic A, Djuricic S, Peterlin B, Mijovic M, Karadzov Orlic N, Egic A, Milovanovic Z

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Clinical Experience of Neurological Mitochondrial Diseases in Children and Adults: A Single-Center Study by Rogac M, Neubauer D, Leonardis L, Pecaric N, Meznaric M, Maver A, Sperl W, Garavaglia BM, Lamantea E, Peterlin B

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Preimplantation Genetic Testing within the Public Healthcare System in Slovenia by Volk M, Writzl K, Veble A, Jaklič H, Teran N, Prosenc B, Štimpfel M, Virant Klun I, Vrtačnik Bokal E, Ban Frangež H, Peterlin B

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Stress from Nucleotide Depletion Activates the Transcriptional Regulator HEXIM1 to Suppress Melanoma by Tan, Justin L., Fogley, Rachel D., Flynn, Ryan A., Ablain, Julien, Yang, Song, Do, Brian T., Laga, Alvaro C., Fujinaga, Koh, Santoriello, Cristina, Greer, Celeste B., Kim, Yoon Jung, Clohessy, John G., Bothmer, Anne, Pandell, Nicole, Avagyan, Serine, Brogie, John E., van Rooijen, Ellen, Hagedorn, Elliott J., Shyh-Chang, Ng, White, Richard M., Price, David H., Pandolfi, Pier Paolo, Peterlin, B. Matija, Zhou, Yi, Kim, Tae Hoon, Asara, John M., Chang, Howard Y., Zon, Leonard I., Saint-André, Violaine, Fan, Zi Peng, Young, Richard A.

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