Works matching IS 20734425 AND DT 2025 AND VI 16 AND IP 1


Results: 109
    1
    2
    3
    4
    5
    6

    Atypical Leber Hereditary Optic Neuropathy (LHON) Associated with a Novel MT-CYB:m.15309T>C(Ile188Thr) Variant.

    Published in:
    Genes, 2025, v. 16, n. 1, p. 108, doi. 10.3390/genes16010108
    By:
    • Petrovic Pajic, Sanja;
    • Fakin, Ana;
    • Jarc-Vidmar, Martina;
    • Sustar Habjan, Maja;
    • Malinar, Lucija;
    • Pavlovic, Kasja;
    • Krako Jakovljevic, Nina;
    • Isakovic, Andjelka;
    • Misirlic-Dencic, Sonja;
    • Volk, Marija;
    • Maver, Ales;
    • Jezernik, Gregor;
    • Glavac, Damjan;
    • Peterlin, Borut;
    • Markovic, Ivanka;
    • Lalic, Nebojsa;
    • Hawlina, Marko
    Publication type:
    Article
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24

    Genotype–Phenotype Correlations of Nance–Horan Syndrome in Male and Female Carriers of a Novel Variant.

    Published in:
    Genes, 2025, v. 16, n. 1, p. 91, doi. 10.3390/genes16010091
    By:
    • Zin, Olivia A.;
    • Neves, Luiza M.;
    • Motta, Fabiana L.;
    • Junior, Daltro C.;
    • Cunha, Daniela P.;
    • Agonigi, Bruna N. S.;
    • Malacarne, Jocieli;
    • Rodrigues, Ana Paula S.;
    • Rodrigues, Gabriela D.;
    • Tinoco, Maria Luisa C.;
    • Horovitz, Dafne D. G.;
    • Carvalho, Adriana B.;
    • Zin, Andrea A.;
    • Vasconcelos, Zilton F. M.;
    • Sallum, Juliana M. Ferraz
    Publication type:
    Article
    25

    Hereditary Breast Cancer: Comprehensive Risk Assessment and Prevention Strategies.

    Published in:
    2025
    By:
    • Manna, Eliza Del Fiol;
    • Serrano, Davide;
    • Cazzaniga, Laura;
    • Mannucci, Sara;
    • Zanzottera, Cristina;
    • Fava, Francesca;
    • Aurilio, Gaetano;
    • Guerrieri-Gonzaga, Aliana;
    • Risti, Matilde;
    • Calvello, Mariarosaria;
    • Feroce, Irene;
    • Marabelli, Monica;
    • Altemura, Cecilia;
    • Bertario, Lucio;
    • Bonanni, Bernardo;
    • Lazzeroni, Matteo
    Publication type:
    Literature Review
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    40
    41
    42
    43
    44
    45
    46
    47

    Genome-Wide Insights into Internalizing Symptoms in Admixed Latin American Children.

    Published in:
    Genes, 2025, v. 16, n. 1, p. 63, doi. 10.3390/genes16010063
    By:
    • Britto, Gabriela de Sales Guerreiro;
    • Moreira, Alberto O.;
    • Bispo Amaral, Edson Henrique;
    • Santos, Daniel Evangelista;
    • São Pedro, Raquel B.;
    • Barreto, Thaís M. M.;
    • Feitosa, Caroline Alves;
    • Neves dos Santos, Darci;
    • Tarazona-Santos, Eduardo;
    • Barreto, Maurício Lima;
    • Figueiredo, Camila Alexandrina Viana de;
    • Costa, Ryan dos Santos;
    • Godard, Ana Lúcia Brunialti;
    • Oliveira, Pablo Rafael Silveira
    Publication type:
    Article
    48
    49
    50

    Novel OTOG Variants and Clinical Features of Hearing Loss in a Large Japanese Cohort.

    Published in:
    Genes, 2025, v. 16, n. 1, p. 60, doi. 10.3390/genes16010060
    By:
    • Arai, Yasuhiro;
    • Nishio, Shin-ya;
    • Goto, Shinichi;
    • Kobayashi, Yumiko;
    • Honkura, Yohei;
    • Ganaha, Akira;
    • Ishikawa, Kotaro;
    • Oka, Shin-ichiro;
    • Futagawa, Hiroshi;
    • Okami, Mayuri;
    • Takada, Fumio;
    • Nagai, Kyoko;
    • Esaki, Tomoko;
    • Okano, Takayuki;
    • Ohta, Yumi;
    • Masuda, Shin;
    • Egusa, Kentaro;
    • Teraoka, Masato;
    • Sugahara, Kazuma;
    • Usami, Shin-ichi
    Publication type:
    Article