نتائج البحث

Opt-in for secondary findings as part of diagnostic whole-exome sequencing: Real-life experience from an international diagnostic laboratory.

• Authors : Brunfeldt M; Finnish Institute for Health and Welfare, Helsinki, Finland.; Kaare M

Subjects: Genetic Testing* ; Genetic Counseling*; Child

• Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Aug; Vol. 11 (8), pp. e2180. Date of Electronic Publication: 2023 Apr 06.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic

تفاصيل العنوان

ULTRALOW COVERAGE SEQUENCING IS THE MOST ACCURATE LIBRARY QUANTIFICATION METHOD PRIOR TO EXOME SEQUENCING.

• Authors : KRASNENKO, Anna Yu.^1,2,3; STETSENKO, Ivan F.^1,2; RAKITKO, Alexander S.^1,4

• Source: Periódico Tchê Química. 2019, Vol. 16 Issue 32, p1010-1016. 7p.

تفاصيل العنوان

Correspondence on 'ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)' by Miller et al

• Authors : McGurk, KA; Zheng, SL; Henry, A ...

Subjects: Science & Technology; Life Sciences & Biomedicine; Genetics & HeredityUnited States

• Source: 746 ; 744

تفاصيل العنوان

Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis - a prospective population-based cohort study.

• Authors : Borghesi, A; Trück, J; Asgari, S ...

Subjects: child; exome sequencing; genomicsUnited States

• Source: e623 ; e614

تفاصيل العنوان

Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.

• Authors : Bowling KM; HudsonAlpha Institute for Biotechnology, Huntsville, AL, 35806, USA.; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.

Subjects: Genome, Human* ; Exome*; Humans

• Source: Genome medicine [Genome Med] 2022 Nov 21; Vol. 14 (1), pp. 131. Date of Electronic Publication: 2022 Nov 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

تفاصيل العنوان

Whole exome sequence-based association analyses of plasma amyloid-β in African and European Americans; the Atherosclerosis Risk in Communities-Neurocognitive Study.

• Authors : Simino J; Gertrude C. Ford MIND Center, University of Mississippi Medical Center, Jackson, Mississippi, United States of America.; Department of Data Science, John D. Bower School of Population Health, University of Mississippi Medical Center, Jackson, Mississippi, United States of America.

Subjects: Polymorphism, Single Nucleotide*; Black or African American/Black or African American/Black or African American/*genetics ; Amyloid beta-Peptides/Amyloid beta-Peptides/Amyloid beta-Peptides/*blood

• Source: PloS one [PLoS One] 2017 Jul 13; Vol. 12 (7), pp. e0180046. Date of Electronic Publication: 2017 Jul 13 (Print Publication: 2017).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

تفاصيل العنوان

Whole-exome sequencing reveals genetic variability among lung cancer cases subphenotyped for emphysema.

• Authors : Lusk, Christine M.^1,2; Wenzlaff, Angela S.^1,2; Dyson, Greg^1,2

Subjects: *LUNG cancer & genetics; *EXOMES; *PUBLIC healthUNITED States

• Source: Carcinogenesis. Feb2016, Vol. 37 Issue 2, p139-144. 6p.

تفاصيل العنوان

Military Health Care Dilemmas and Genetic Discrimination: A Family's Experience with Whole Exome Sequencing.

• Authors : Helm BM; Langley K; Spangler BB

Subjects: Disclosure* ; Employment* ; Genetic Testing*

• Source: Narrative inquiry in bioethics [Narrat Inq Bioeth] 2015 Summer; Vol. 5 (2), pp. 179-86.Publisher: Johns Hopkins University Press Country of Publication: United States NLM ID: 101603418 Publication Model: Print

تفاصيل العنوان

Exome-Wide Association Study of Endometrial Cancer in a Multiethnic Population.

• Authors : Chen, Maxine M.¹; Crous-Bou, Marta^1,2; Setiawan, Veronica W.³

Subjects: *CANCER-related mortality; *CANCER; *ENDOMETRIAL cancer risk factorsUNITED States

• Source: PLoS ONE. May2014, Vol. 9 Issue 5, p1-9. 9p.

تفاصيل العنوان

Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.

• Authors : Esslinger, U; Garnier, S; Korniat, A

Subjects: General Science & TechnologyUnited States

• Source: e0229472

تفاصيل العنوان