275 related articles for article (PubMed ID: 29986673)
21. Parents' experiences of newborn screening for genetic susceptibility to type 1 diabetes.
Kerruish NJ
J Med Ethics; 2011 Jun; 37(6):348-53. PubMed ID: 21266388
[TBL] [Abstract][Full Text] [Related]
22. [Genomic newborn screening. Perspective from the Ethics commission of the Spanish Society for Human Genetics. Part I. Next generation sequencing technologies applied to newborn screening. Challenges and opportunities.].
Pàmpols Ros T; Pérez Aytés A; García Sagredo JM; Díaz de Bustamante A; Blanco Guillermo I
Rev Esp Salud Publica; 2022 Feb; 96():. PubMed ID: 35115483
[TBL] [Abstract][Full Text] [Related]
23. The Legal Dimensions of Genomic Sequencing in Newborn Screening.
Zacharias RL; Smith ME; King JS
Hastings Cent Rep; 2018 Jul; 48 Suppl 2():S39-S41. PubMed ID: 30133728
[TBL] [Abstract][Full Text] [Related]
24. [Genomic newborn screening. Perspective from the Ethics Commission of the Spanish Society for Human Genetics. Part II: Ethical, legal and social issues (ELSIs) of the introduction of next generation sequencing technologies in a public health newborn screening program.].
Pàmpols Ros T; Pérez Aytés A; García Sagredo JM; Díaz de Bustamante A; Blanco Guillermo I
Rev Esp Salud Publica; 2022 Mar; 96():. PubMed ID: 35283479
[TBL] [Abstract][Full Text] [Related]
25. Genetic counseling and neonatal screening for cystic fibrosis: an assessment of the communication process.
Ciske DJ; Haavisto A; Laxova A; Rock LZ; Farrell PM
Pediatrics; 2001 Apr; 107(4):699-705. PubMed ID: 11335747
[TBL] [Abstract][Full Text] [Related]
26. Challenges of using next generation sequencing in newborn screening.
Reinstein E
Genet Res (Camb); 2015 Nov; 97():e21. PubMed ID: 26521961
[TBL] [Abstract][Full Text] [Related]
27. Commercial Interests, the Technological Imperative, and Advocates: Three Forces Driving Genomic Sequencing in Newborns.
Pereira S; Clayton EW
Hastings Cent Rep; 2018 Jul; 48 Suppl 2():S43-S44. PubMed ID: 30133724
[TBL] [Abstract][Full Text] [Related]
28. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Vassy JL; Lautenbach DM; McLaughlin HM; Kong SW; Christensen KD; Krier J; Kohane IS; Feuerman LZ; Blumenthal-Barby J; Roberts JS; Lehmann LS; Ho CY; Ubel PA; MacRae CA; Seidman CE; Murray MF; McGuire AL; Rehm HL; Green RC;
Trials; 2014 Mar; 15():85. PubMed ID: 24645908
[TBL] [Abstract][Full Text] [Related]
29. [Newborn screening for primary carnitine deficiency and variant spectrum of SLC22A5 gene in Guangzhou].
Huang YL; Tang CF; Liu SC; Sheng HY; Tang F; Jiang X; Zheng RD; Mei HF; Liu L
Zhonghua Er Ke Za Zhi; 2020 Jun; 58(6):476-481. PubMed ID: 32521959
[No Abstract] [Full Text] [Related]
30. Parents' interest in whole-genome sequencing of newborns.
Goldenberg AJ; Dodson DS; Davis MM; Tarini BA
Genet Med; 2014 Jan; 16(1):78-84. PubMed ID: 23743552
[TBL] [Abstract][Full Text] [Related]
31. RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
Elliott AM; du Souich C; Lehman A; Guella I; Evans DM; Candido T; Tooman L; Armstrong L; Clarke L; Gibson W; Gill H; Lavoie PM; Lewis S; McKinnon ML; Nikkel SM; Patel M; Solimano A; Synnes A; Ting J; van Allen M; Christilaw J; Farrer MJ; Friedman JM; Osiovich H
Eur J Pediatr; 2019 Aug; 178(8):1207-1218. PubMed ID: 31172278
[TBL] [Abstract][Full Text] [Related]
32. A curated gene list for reporting results of newborn genomic sequencing.
Ceyhan-Birsoy O; Machini K; Lebo MS; Yu TW; Agrawal PB; Parad RB; Holm IA; McGuire A; Green RC; Beggs AH; Rehm HL
Genet Med; 2017 Jul; 19(7):809-818. PubMed ID: 28079900
[TBL] [Abstract][Full Text] [Related]
33. Psychosocial Factors Influencing Parental Interest in Genomic Sequencing of Newborns.
Waisbren SE; Weipert CM; Walsh RC; Petty CR; Green RC
Pediatrics; 2016 Jan; 137 Suppl 1(Suppl 1):S30-5. PubMed ID: 26729701
[TBL] [Abstract][Full Text] [Related]
34. Whole exome or genome sequencing: nurses need to prepare families for the possibilities.
Prows CA; Tran G; Blosser B
J Adv Nurs; 2014 Dec; 70(12):2736-45. PubMed ID: 25175401
[TBL] [Abstract][Full Text] [Related]
35. An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening.
Milko LV; O'Daniel JM; DeCristo DM; Crowley SB; Foreman AKM; Wallace KE; Mollison LF; Strande NT; Girnary ZS; Boshe LJ; Aylsworth AS; Gucsavas-Calikoglu M; Frazier DM; Vora NL; Roche MI; Powell BC; Powell CM; Berg JS
J Pediatr; 2019 Jun; 209():68-76. PubMed ID: 30851990
[TBL] [Abstract][Full Text] [Related]
36. Genetic profiling of newborns: ethical and social issues.
Almond B
Nat Rev Genet; 2006 Jan; 7(1):67-71. PubMed ID: 16369573
[TBL] [Abstract][Full Text] [Related]
37. Preconception genome medicine: current state and future perspectives to improve infertility diagnosis and reproductive and health outcomes based on individual genomic data.
Capalbo A; Poli M; Riera-Escamilla A; Shukla V; Kudo Høffding M; Krausz C; Hoffmann ER; Simon C
Hum Reprod Update; 2021 Feb; 27(2):254-279. PubMed ID: 33197264
[TBL] [Abstract][Full Text] [Related]
38. Personal utility of genomic sequencing for infants with congenital deafness.
Tutty E; Amor DJ; Jarmolowicz A; Paton K; Downie L
Am J Med Genet A; 2021 Dec; 185(12):3634-3643. PubMed ID: 34184819
[TBL] [Abstract][Full Text] [Related]
39. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
[TBL] [Abstract][Full Text] [Related]
40. A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism.
Wang W; Yang J; Xue J; Mu W; Zhang X; Wu W; Xu M; Gong Y; Liu Y; Zhang Y; Xie X; Gu W; Bai J; Cram DS
BMC Med Genet; 2019 Jan; 20(1):3. PubMed ID: 30612563
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
