Response to Mounts and Besser

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FOXR2-activated CNS neuroblastoma: Characterized by variable structural disruption of the <i>FOXR2</i> regulatory region, recurrent copy number alterations, and elevated <i>FOXR2</i> expression.

Neuro-oncology pediatrics·2026

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Germline genetic testing and privacy concerns in patients with mesothelioma.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

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Investigating Genetic Risk to Oxaliplatin-Induced Sinusoidal Obstruction Syndrome in Colorectal Cancer Through Routinely Available Next-Generation Sequencing Data.

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc·2026

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Spinal muscular atrophy among US Hutterites: Phenotype variability in the setting of conserved ancestral haplotype and 4 SMN2 copies.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

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Sialidosis type I: How to alleviate disabling myoclonic seizures?-A multicenter analysis of eight cases and review of the literature.

Epilepsia open·2026

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Points to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG).

Genetics in medicine : official journal of the American College of Medical Genetics·2026

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RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Same journal

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Same journal

Delineating the clinical and molecular spectrum of the neurodevelopmental disorder associated with SET.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Same journal

KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Same journal

Beyond Mistrust: Diverse Biobanking Preferences Among Parents and Adolescents with Sickle Cell Disease.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

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Correspondence on "Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome mechanisms" by Pastor et al.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Related Experiment Videos

Response to Mounts and Besser

Related Concept Videos

FOXR2-activated CNS neuroblastoma: Characterized by variable structural disruption of the <i>FOXR2</i> regulatory region, recurrent copy number alterations, and elevated <i>FOXR2</i> expression.

Germline genetic testing and privacy concerns in patients with mesothelioma.

Investigating Genetic Risk to Oxaliplatin-Induced Sinusoidal Obstruction Syndrome in Colorectal Cancer Through Routinely Available Next-Generation Sequencing Data.

Spinal muscular atrophy among US Hutterites: Phenotype variability in the setting of conserved ancestral haplotype and 4 SMN2 copies.

Sialidosis type I: How to alleviate disabling myoclonic seizures?-A multicenter analysis of eight cases and review of the literature.

Points to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG).

RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Delineating the clinical and molecular spectrum of the neurodevelopmental disorder associated with SET.

KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.

Beyond Mistrust: Diverse Biobanking Preferences Among Parents and Adolescents with Sickle Cell Disease.

Correspondence on "Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome mechanisms" by Pastor et al.

Related Experiment Videos

Response to Mounts and Besser

Related Concept Videos

Related Articles

FOXR2-activated CNS neuroblastoma: Characterized by variable structural disruption of the <i>FOXR2</i> regulatory region, recurrent copy number alterations, and elevated <i>FOXR2</i> expression.

Germline genetic testing and privacy concerns in patients with mesothelioma.

Investigating Genetic Risk to Oxaliplatin-Induced Sinusoidal Obstruction Syndrome in Colorectal Cancer Through Routinely Available Next-Generation Sequencing Data.

Spinal muscular atrophy among US Hutterites: Phenotype variability in the setting of conserved ancestral haplotype and 4 SMN2 copies.

Sialidosis type I: How to alleviate disabling myoclonic seizures?-A multicenter analysis of eight cases and review of the literature.

Points to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG).

RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Delineating the clinical and molecular spectrum of the neurodevelopmental disorder associated with SET.

KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.

Beyond Mistrust: Diverse Biobanking Preferences Among Parents and Adolescents with Sickle Cell Disease.

Correspondence on "Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome mechanisms" by Pastor et al.