Use of large-scale sample collections to estimate the carriage rate of miscarriage-related variants by Yu. A. Barbitov, T. E. Lazareva, Yu. A. Nasykhova, O. N. Bespalova, A. S. Glotov

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The relationship between cathepsins and nasopharyngeal carcinoma: a Mendelian randomization analysis by Jiaxiang Hu, Keyun Lin, Mei Jiang, Guanying Qiao

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Novel biallelic MCMDC2 variants were associated with meiotic arrest and nonobstructive azoospermia by Hao-Wei Bai, Na Li, Yu-Xiang Zhang, Jia-Qiang Luo, Ru-Hui Tian, Peng Li, Yu-Hua Huang, Fu-Rong Bai, Cun-Zhong Deng, Fu-Jun Zhao, Ren Mo, Ning Chi, Yu-Chuan Zhou, Zheng Li, Chen-Cheng Yao, Er-Lei Zhi

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The role of genetic hemostasis gene variants in the development of venous thrombosis in patients with atherosclerosis after COVID-19 infection by O. A Perevezentsev, I. S. Mamedov, D. V. Burtsev

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Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype by Hussein Alhawari, Zaina Obeidat, Lina Wahbeh, Ayman Mismar, Nedal Younis, Hanan Jafar, Munther Momani, Nedal Alsabatin, Abdalla Awidi, Hussam Alhawari

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Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencing by Jeong-Min Kim, Hye-Won Cho, Dong Mun Shin, Oc-Hee Kim, Jihyun Kim, Hyeji Lee, Gang-Hee Lee, Joon-Yong An, Misun Yang, Heui Seung Jo, Ja-Hyun Jang, Yun Sil Chang, Hyun-Young Park, Mi-Hyun Park

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Enhancing the utility of polygenic scores in Alzheimer’s disease through systematic curation and annotation by Savannah Mwesigwa, Yulin Dai, Nitesh Enduru, Zhongming Zhao, Zhongming Zhao

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Genetic and phenotypic characteristics of 3 patients with limb-girdle muscular dystrophy: experience in a medical center in Mexico by Valentina Martínez-Montoya, Alejandro Martínez-Herrera, Oscar Mancera-Páez, Alberto Hidalgo-Bravo, María R. Rivera-Vega

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Multi-omics analysis for identifying cell-type-specific and bulk-level druggable targets in Alzheimer’s disease by Shiwei Liu, Minyoung Cho, Yen-Ning Huang, Tamina Park, Soumilee Chaudhuri, Thea J. Rosewood, Paula J. Bice, Dongjun Chung, David A. Bennett, Nilüfer Ertekin-Taner, Andrew J. Saykin, Kwangsik Nho

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Impact of tumor necrosis factor-alpha gene variant in pediatric nephrotic syndrome: a meta-analysis by Yogalakshmi Venkatachalapathy, Praveenkumar Kochuthakidiyel Suresh, Thendral Hepsibha Balraj, Vettriselvi Venkatesan, Sangeetha Geminiganesan, Indira Bhagam, C. D. Mohana Priya

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Dietary acid load adopts the effect of ApoB ins/del genetic variant (rs11279109) on obesity trait, cardiovascular markers, lipid profile, and serum leptin level among patients with... by Zahra Esmaeily, Faezeh Abaj, Zeinab Naeini, Ehsan Alvandi, Masoumeh Rafiee, Fariba Koohdani

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Editorial: Case reports in nephrology by Xuefei Tian, Leopoldo Ardiles, Clay A. Block

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CCDC82 and neurodevelopment: a novel genetic variant linked to infantile spasms and hypotonia by Zahra Safarian, Shiva Mehrabi, Arghavan Rakhshani Nejad, Sajad Alavimanesh, Pegah Kavousinia, Mohammad Hossein Shushizadeh, Seyedeh Faezeh Hassani, Latifeh Onagh, Abdolazim Sarli, Nahid Rezaie

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The novel SERPINC1 missense mutation c.1148 T > A (p.L383H) causes hereditary antithrombin deficiency and thromboembolism in a Chinese family: a case report by Fangkai He, Yang Wang, Weiwei Ning, Chao Liu, Xiaojun Guan, Yao Yao

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Massive dissemination of a SARS-CoV-2 Spike Y839 variant in Portugal by Vítor Borges, Joana Isidro, Helena Cortes-Martins, Sílvia Duarte, Luís Vieira, Ricardo Leite, Isabel Gordo, Constantino P. Caetano, Baltazar Nunes, Regina Sá, Ana Oliveira, Raquel Guiomar, João Paulo Gomes

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Epidemiological Evaluation of Neuter Status, Sex, and Breed in Dogs With Cystine Uroliths by Jody P. Lulich, Rachael Ulrich, Eva Furrow

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Barrier genes are associated with preterm birth by Kuan-Ru Chen, Shih-Kai Chu, Pao-Lin Kuo, Pao-Lin Kuo, Pao-Lin Kuo

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Bioinformatics pipeline to guide late‐onset Alzheimer's disease (LOAD) post‐GWAS studies: Prioritizing transcription regulatory variants within LOAD‐associated regions by Michael W. Lutz, Ornit Chiba‐Falek

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Studying of the effect of the genetic variant c.470T>C in the CHEK2 gene on increasing the risk of breast cancer in the population of the Russian Federation by E. I. Novikova, V. K. Bozhenko, E. A. Kudinova, V. A. Solodkiy

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Genetic insights from a Brazilian cohort of aortopathies through targeted next-generation sequencing and FBN1 direct sequencing by Juliana Rocha Ferreira, Julia Passarelli Pereira, Anna Paula Arpini Botelho, Daniele do Nascimento Aprijo, Marcelo Machado Melo, Helena Cramer Veiga Rey, Glauber Monteiro Dias

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