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91. Genetic basis of ear length in sheep breeds sampled across the region from the Middle East to the Alps
Jürgen Klawatsch, Dimitris Papachristou, Panagiota Koutsouli, Maulik Upadhyay, Doris Seichter, Ingolf Russ, Boro Mioč, Mojca Simčič, Iosif Bizelis, Ivica Medjugorac, 2024, original scientific article

Keywords: ear length, genetic mapping, ruminants, sheep
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92. Phytosulfokine alpha enhances regeneration of transformed and untransformed protoplasts of Brassica oleracea
Valentin Vogrinčič, Damijana Kastelec, Jana Murovec, 2024, original scientific article

Keywords: PSK-α, cell division, differentiation, organogenesis, alginate disc, genetic transformation, plant genome editing, plasmid
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93. Genetic algorithm-based framework for optimization of laser beam path in additive manufacturing
Primož Potočnik, Andrej Jeromen, Edvard Govekar, 2024, original scientific article

Keywords: additive manufacturing, laser beam path, genetic algorithm, optimization
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94. The clinical spectrum and disease course of DRAM2 retinopathy
Tjaša Krašovec, Marija Volk, Maja Šuštar Habjan, Marko Hawlina, Nataša Vidović Valentinčič, Ana Fakin, 2022, original scientific article

Keywords: DRAM2, inherited retinal dystrophy, genetic spectrum, phenotype variability, genotype–phenotype correlation, fundus autofluorescence imaging, electrophysiology
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95. Genetic algorithm-based optimization of the laser-beam path in additive manufacturing
Primož Potočnik, Andrej Jeromen, Edvard Govekar, 2024, original scientific article

Keywords: additive manufacturing, laser beam path, genetic algorithm, optimization
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96. The genetic approach to stillbirth
Maja Dolanc Merc, Borut Peterlin, Luca Lovrečić, 2023, original scientific article

Keywords: stillbirth, genetic approach, genetics, human
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97. Modelling a response of complex-phase steel at high strain rates
Andrej Škrlec, Tadej Kocjan, Marko Nagode, Jernej Klemenc, 2024, original scientific article

Keywords: complex phase steel, Cowper–Symonds model, response surface, multi-criterion objective function, genetic algorithm
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98. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency
Nina Rupar, Julij Šelb, Mitja Košnik, Mihaela Zidarn, Slađana Andrejević, Ljerka Čulav, Vesna Grivčeva-Panovska, Peter Korošec, Matija Rijavec, 2024, original scientific article

Keywords: hereditary angioedema, C1 inhibitor deficiency, genetic modifiers, clinical phenotype, genotype-phenotype correlation, genetic variant, SERPING1, CC2D2B
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