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Academic Journal

Cascade testing for hereditary cancer in Singapore: how population genomics help guide clinical policy.

  • Authors : Caeser R; Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, 169610, Singapore.; Oncology Academic Clinical Program, Duke-NUS Medical School, Singapore, Singapore.

Subjects: Genetic Testing*/Genetic Testing*/Genetic Testing*/methods ; Genomics*/Genomics*/Genomics*/methods ; Genetic Predisposition to Disease*

  • Source: Familial cancer [Fam Cancer] 2024 Jun; Vol. 23 (2), pp. 133-140. Date of Electronic Publication: 2024 Apr 25.Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populations.

  • Authors : Cohen ASA; Genomic Medicine Center, Children's Mercy Kansas City, Kansas City, MO 64108, USA; Department of Pathology and Laboratory Medicine, Children's Mercy Kansas City, Kansas City, MO 64108, USA

Subjects: Rural Population* ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methods ; Rare Diseases*/Rare Diseases*/Rare Diseases*/genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2024 May 02; Vol. 111 (5), pp. 825-832. Date of Electronic Publication: 2024 Apr 17.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Interpreting and integrating genomic tests results in clinical cancer care: Overview and practical guidance.

  • Authors : Casolino R; Wolfson Wohl Cancer Research Center, School of Cancer Sciences, University of Glasgow, Glasgow, UK.; Beer PA

Subjects: Neoplasms*/Neoplasms*/Neoplasms*/genetics ; Neoplasms*/Neoplasms*/Neoplasms*/therapy ; Neoplasms*/Neoplasms*/Neoplasms*/diagnosis

  • Source: CA: a cancer journal for clinicians [CA Cancer J Clin] 2024 May-Jun; Vol. 74 (3), pp. 264-285. Date of Electronic Publication: 2024 Jan 04.Publisher: Wiley Country of Publication: United States NLM ID: 0370647 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1542-4863

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Academic Journal

Genomic multidisciplinary teams: A model for navigating genetic mainstreaming and precision medicine.

  • Authors : Ma A; Department of Clinical Genetics, Sydney Children's Hospitals Network - Westmead, Sydney, New South Wales, Australia.; Specialty of Genomic Medicine, University of Sydney, Sydney, New South Wales, Australia.

Subjects: Precision Medicine*/Precision Medicine*/Precision Medicine*/methods ; Patient Care Team* ; Genomics*

  • Source: Journal of paediatrics and child health [J Paediatr Child Health] 2024 Apr-May; Vol. 60 (4-5), pp. 118-124. Date of Electronic Publication: 2024 Apr 11.Publisher: Blackwell Scientific Publications Country of Publication: Australia NLM ID: 9005421 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa.

  • Authors : Oladayo AM; Department Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City, Iowa, USA.; Iowa Institute of Oral Health Research, University of Iowa, Iowa City, Iowa, USA.

Subjects: Cleft Palate*/Cleft Palate*/Cleft Palate*/genetics ; Genetic Testing* ; Parents*

  • Source: AJOB empirical bioethics [AJOB Empir Bioeth] 2024 Apr-Jun; Vol. 15 (2), pp. 133-146. Date of Electronic Publication: 2024 Jan 18.Publisher: Taylor & Francis Group, 2014- Country of Publication: United States NLM ID: 101631047 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

The expanding diagnostic toolbox for rare genetic diseases.

  • Authors : Kernohan KD; CHEO Research Institute, University of Ottawa, Ottawa, ON, Canada.; Newborn Screening Ontario, CHEO, Ottawa, ON, Canada.

Subjects: Rare Diseases*/Rare Diseases*/Rare Diseases*/genetics ; Rare Diseases*/Rare Diseases*/Rare Diseases*/diagnosis ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methods

  • Source: Nature reviews. Genetics [Nat Rev Genet] 2024 Jun; Vol. 25 (6), pp. 401-415. Date of Electronic Publication: 2024 Jan 18.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 100962779 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Discussion of off-target and tentative genomic findings may sometimes be necessary to allow evaluation of their clinical significance.

  • Authors : Horton RH; Clinical Ethics, Law and Society, Wellcome Trust Centre for Human Genetics, Oxford, UK.; Centre for Personalised Medicine, St Anne's College, Oxford, UK.

Subjects: Genomics*/Genomics*/Genomics*/ethics ; Genetic Testing*/Genetic Testing*/Genetic Testing*/ethics; Humans

  • Source: Journal of medical ethics [J Med Ethics] 2024 May 09; Vol. 50 (5), pp. 295-298. Date of Electronic Publication: 2024 May 09.Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 7513619 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Gene selection for genomic newborn screening: Moving toward consensus?

  • Authors : Downie L; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia; Murdoch Children's Research Institute, Melbourne, VIC, Australia

Subjects: Neonatal Screening*/Neonatal Screening*/Neonatal Screening*/methods ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methods ; Genetic Testing*/Genetic Testing*/Genetic Testing*/standards

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 May; Vol. 26 (5), pp. 101077. Date of Electronic Publication: 2024 Jan 23.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

More Than a Decade of Rapid Genomic Sequencing: Where Are We Now?

  • Authors : Saunders CJ; Director, Division of Genetics and Genomics Laboratory, Department of Pathology and Laboratory Medicine, Children's Mercy-Kansas City, Professor of Pediatrics and Pathology, University of Missouri-Kansas City School of Medicine, Kansas City, MO, United States.; Brunelli L

Subjects: Genetic Testing* ; Genomics*; Humans

  • Source: Clinical chemistry [Clin Chem] 2024 Apr 03; Vol. 70 (4), pp. 577-583.Publisher: Oxford University Press Country of Publication: England NLM ID: 9421549 Publication Model: Print Cited Medium: Internet ISSN:

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Periodical

Super-speedy sequencing puts genomic diagnosis in the fast lane.

Subjects: Genomics*/Genomics*/Genomics*/methods ; Genomics*/Genomics*/Genomics*/trends ; High-Throughput Nucleotide Sequencing*/High-Throughput Nucleotide Sequencing*/High-Throughput Nucleotide Sequencing*/methods

  • Source: Nature [Nature] 2024 Feb; Vol. 626 (8000), pp. 915-917.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 0410462 Publication Model: Print Cited Medium: Internet ISSN:

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  • 1-10 of  10,324 results for ""Genomics""