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  • 10.1016/j.gim.2025.101559
Correspondence on “Estimation of carrier frequencies of autosomal and X-linked recessive genetic conditions based on gnomAD v4.0 data in different ancestries” by Hotakainen et al
  • Dec 1, 2025
  • Genetics in Medicine
  • Mia J Gruzin + 2 more

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  • 10.1016/j.gim.2025.101560
Response to Gruzin et al
  • Dec 1, 2025
  • Genetics in Medicine
  • Ronja Hotakainen + 3 more

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  • 10.1016/s1098-3600(25)00293-x
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  • Dec 1, 2025
  • Genetics in Medicine

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  • 10.1016/s1098-3600(25)00291-6
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  • 10.1016/s1098-3600(25)00292-8
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  • 10.1016/s1098-3600(25)00228-x
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  • Genetics in Medicine

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  • 10.1016/j.gim.2025.101623
De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadism.
  • Oct 1, 2025
  • Genetics in Medicine
  • Maria Stamou + 19 more

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  • 10.1016/s1098-3600(25)00229-1
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  • Oct 1, 2025
  • Genetics in Medicine

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  • 10.1016/s1098-3600(25)00227-8
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  • Oct 1, 2025
  • Genetics in Medicine

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  • 10.1016/j.gim.2025.101620
Charting the Phenotypic Landscape of Mitochondrial Diseases through a Systematic Evaluation of Pathogenic Mitochondrial DNA and Nuclear Gene Variants
  • Oct 1, 2025
  • Genetics in Medicine
  • Thiloka Ratnaike + 14 more