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Items: 1 to 50 of 138

1.

Challenges to informed consent for exome sequencing: A best-worst scaling experiment.

Gore RH, Bridges JFP, Cohen JS, Biesecker BB.

J Genet Couns. 2019 Sep 25. doi: 10.1002/jgc4.1171. [Epub ahead of print]

PMID:
31553105
2.

Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial.

Umstead KL, Han PKJ, Lewis KL, Miller IM, Hepler CL, Thompson LJ, Wolfsberg TG, Nguyen AD, Fredriksen MT, Gibney G, Turbitt E, Biesecker LG, Biesecker BB.

Transl Behav Med. 2019 Aug 31. pii: ibz111. doi: 10.1093/tbm/ibz111. [Epub ahead of print]

PMID:
31505002
3.

The Psychological Well-being of Pregnant Women Undergoing Prenatal Testing and Screening: A Narrative Literature Review.

Biesecker BB.

Hastings Cent Rep. 2019 May;49 Suppl 1:S53-S60. doi: 10.1002/hast.1017.

PMID:
31268571
4.

High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease.

Berrios CD, Chakravarti A, Biesecker BB.

J Pediatr Gastroenterol Nutr. 2019 Sep;69(3):299-305. doi: 10.1097/MPG.0000000000002392.

PMID:
31107799
5.

Uncertainty, hope, and coping efficacy among mothers of children with Duchenne/Becker muscular dystrophy.

Bell M, Biesecker BB, Bodurtha J, Peay HL.

Clin Genet. 2019 Jun;95(6):677-683. doi: 10.1111/cge.13528. Epub 2019 Apr 3.

PMID:
30847900
6.

Managing the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore.

Kumar N, Turbitt E, Biesecker BB, Miller IM, Cham B, Smith KC, Rimal RN.

Am J Med Genet A. 2019 May;179(5):762-769. doi: 10.1002/ajmg.a.61107. Epub 2019 Mar 1.

PMID:
30821068
7.

Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey.

Turbitt E, Roberts MC, Taber JM, Waters EA, McNeel TS, Biesecker BB, Klein WMP.

Prev Med. 2019 Jun;123:12-19. doi: 10.1016/j.ypmed.2019.02.027. Epub 2019 Feb 25.

PMID:
30817954
8.

A primer in genomics for social and behavioral investigators.

Turbitt E, Biesecker BB.

Transl Behav Med. 2019 Feb 22. pii: ibz018. doi: 10.1093/tbm/ibz018. [Epub ahead of print]

PMID:
30793199
9.

Fragile X syndrome clinical trials: exploring parental decision-making.

D'Amanda CS, Peay HL, Wheeler AC, Turbitt E, Biesecker BB.

J Intellect Disabil Res. 2019 Aug;63(8):926-935. doi: 10.1111/jir.12605. Epub 2019 Feb 12.

PMID:
30747463
10.

Noninvasive Prenatal Whole Genome Sequencing: Pregnant Women's Views and Preferences.

Sullivan HK, Bayefsky M, Wakim PG, Huddleston K, Biesecker BB, Hull SC, Berkman BE.

Obstet Gynecol. 2019 Mar;133(3):525-532. doi: 10.1097/AOG.0000000000003121.

PMID:
30741804
11.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.

Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, Ghazani AA, Gilmore MJ, Goddard KAB, Jarvik GP, Johnston JJ, Kauffman TL, Kelley WV, Krier JB, Lewis KL, McGuire AL, McMullen C, Ou J, Plon SE, Rehm HL, Richards CS, Romasko EJ, Sagardia AM, Spinner NB, Thompson ML, Turbitt E, Vassy JL, Wilfond BS, Veenstra DL, Berg JS, Green RC, Biesecker LG, Hindorff LA.

Genet Med. 2019 May;21(5):1261-1262. doi: 10.1038/s41436-019-0440-2.

PMID:
30670880
12.

A behavior-theoretic evaluation of values clarification on parental beliefs and intentions toward genomic sequencing for newborns.

Paquin RS, Peinado S, Lewis MA, Biesecker BB, Rini C, Roche M, Butterfield RM, Powell CM, Berg JS, Bailey DB Jr.

Soc Sci Med. 2018 Nov 9. pii: S0277-9536(18)30651-8. doi: 10.1016/j.socscimed.2018.11.017. [Epub ahead of print]

PMID:
30448267
13.

Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort.

Lewis KL, Heidlebaugh AR, Epps S, Han PKJ, Fishler KP, Klein WMP, Miller IM, Ng D, Hepler C, Biesecker BB, Biesecker LG.

Genet Med. 2019 Jun;21(6):1355-1362. doi: 10.1038/s41436-018-0341-9. Epub 2018 Nov 1.

PMID:
30382154
14.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.

Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, Ghazani AA, Gilmore MJ, Goddard KAB, Jarvik GP, Johnston JJ, Kauffman TL, Kelley WV, Krier JB, Lewis KL, McGuire AL, McMullen C, Ou J, Plon SE, Rehm HL, Richards CS, Romasko EJ, Miren Sagardia A, Spinner NB, Thompson ML, Turbitt E, Vassy JL, Wilfond BS, Veenstra DL, Berg JS, Green RC, Biesecker LG, Hindorff LA.

Genet Med. 2019 May;21(5):1100-1110. doi: 10.1038/s41436-018-0308-x. Epub 2018 Oct 5. Erratum in: Genet Med. 2019 Jan 22;:.

PMID:
30287922
15.

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.

Amendola LM, Berg JS, Horowitz CR, Angelo F, Bensen JT, Biesecker BB, Biesecker LG, Cooper GM, East K, Filipski K, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hassmiller-Lich K, Joseph G, Kenny EE, Koenig BA, Knight S, Kwok PY, Lewis KL, McGuire AL, Norton ME, Ou J, Parsons DW, Powell BC, Risch N, Robinson M, Rini C, Scollon S, Slavotinek AM, Veenstra DL, Wasserstein MP, Wilfond BS, Hindorff LA; CSER consortium, Plon SE, Jarvik GP.

Am J Hum Genet. 2018 Sep 6;103(3):319-327. doi: 10.1016/j.ajhg.2018.08.007.

16.

Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.

Sapp JC, Johnston JJ, Driscoll K, Heidlebaugh AR, Miren Sagardia A, Dogbe DN, Umstead KL, Turbitt E, Alevizos I, Baron J, Bönnemann C, Brooks B, Donkervoort S, Jee YH, Linehan WM, McMahon FJ, Moss J, Mullikin JC, Nielsen D, Pelayo E, Remaley AT, Siegel R, Su H, Zarate C; NISC Comparative Sequencing Program, Manolio TA, Biesecker BB, Biesecker LG.

Am J Hum Genet. 2018 Sep 6;103(3):358-366. doi: 10.1016/j.ajhg.2018.07.018. Epub 2018 Aug 16.

17.

Decision role preferences for return of results from genome sequencing amongst young breast cancer patients.

Matsen CB, Lyons S, Goodman MS, Biesecker BB, Kaphingst KA.

Patient Educ Couns. 2019 Jan;102(1):155-161. doi: 10.1016/j.pec.2018.08.004. Epub 2018 Aug 4.

PMID:
30098907
18.

Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes.

Miller IM, Lewis KL, Lawal TA, Ng D, Johnston JJ, Biesecker BB, Biesecker LG.

Genet Med. 2019 Mar;21(3):748-752. doi: 10.1038/s41436-018-0083-8. Epub 2018 Jul 12.

19.

Web-Based Platform vs Genetic Counselors in Educating Patients About Carrier Results From Exome Sequencing-Reply.

Biesecker BB, Lewis KL, Biesecker LG.

JAMA Intern Med. 2018 Jul 1;178(7):999. doi: 10.1001/jamainternmed.2018.2236. No abstract available.

PMID:
29971366
20.

Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications.

Hellwig LD, Biesecker BB, Lewis KL, Biesecker LG, James CA, Klein WMP.

Circ Genom Precis Med. 2018 Jun;11(6):e001975. doi: 10.1161/CIRCGEN.117.001975.

21.

Associations of perceived norms with intentions to learn genomic sequencing results: Roles for attitudes and ambivalence.

Reid AE, Taber JM, Ferrer RA, Biesecker BB, Lewis KL, Biesecker LG, Klein WMP.

Health Psychol. 2018 Jun;37(6):553-561. doi: 10.1037/hea0000579. Epub 2018 May 10.

22.

Genetic counselors as social and behavioral scientists in the era of precision medicine.

Biesecker BB.

Am J Med Genet C Semin Med Genet. 2018 Mar;178(1):10-14. doi: 10.1002/ajmg.c.31609.

PMID:
29675992
23.

Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing.

Biesecker BB, Woolford SW, Klein WMP, Brothers KB, Umstead KL, Lewis KL, Biesecker LG, Han PKJ.

Clin Genet. 2018 May;93(5):1119. doi: 10.1111/cge.13241. No abstract available.

PMID:
29655271
24.

Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial.

Lewis KL, Umstead KL, Johnston JJ, Miller IM, Thompson LJ, Fishler KP, Biesecker LG, Biesecker BB.

Am J Hum Genet. 2018 Apr 5;102(4):540-546. doi: 10.1016/j.ajhg.2018.02.009. Epub 2018 Mar 8.

25.

Intentions to share exome sequencing results with family members: exploring spousal beliefs and attitudes.

Turbitt E, Roberts MC, Ferrer RA, Taber JM, Lewis KL, Biesecker LG, Biesecker BB, Klein WM.

Eur J Hum Genet. 2018 May;26(5):735-739. doi: 10.1038/s41431-018-0118-2. Epub 2018 Feb 23.

26.

Barriers and facilitators to clinical trial participation among parents of children with pediatric neuromuscular disorders.

Peay HL, Biesecker BB, Wilfond BS, Jarecki J, Umstead KL, Escolar DM, Tibben A.

Clin Trials. 2018 Apr;15(2):139-148. doi: 10.1177/1740774517751118. Epub 2018 Feb 23.

27.

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study.

Turbitt E, Chrysostomou PP, Peay HL, Heidlebaugh AR, Nelson LM, Biesecker BB.

Eur J Hum Genet. 2018 May;26(5):622-630. doi: 10.1038/s41431-018-0105-7. Epub 2018 Feb 16.

28.

50 Years Ago in The Journal of Pediatrics: The Rationale for Genetic Counseling.

Biesecker BB, Biesecker LG.

J Pediatr. 2018 Feb;193:33. doi: 10.1016/j.jpeds.2017.12.037. No abstract available.

PMID:
29389452
29.

Disclosure of cardiac variants of uncertain significance results in an exome cohort.

Lawal TA, Lewis KL, Johnston JJ, Heidlebaugh AR, Ng D, Gaston-Johansson FG, Klein WMP, Biesecker BB, Biesecker LG.

Clin Genet. 2018 May;93(5):1022-1029. doi: 10.1111/cge.13220. Epub 2018 Mar 2.

30.

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.

Biesecker BB, Lewis KL, Umstead KL, Johnston JJ, Turbitt E, Fishler KP, Patton JH, Miller IM, Heidlebaugh AR, Biesecker LG.

JAMA Intern Med. 2018 Mar 1;178(3):338-346. doi: 10.1001/jamainternmed.2017.8049.

31.

Self-Regulation Principles Underlying Risk Perception and Decision Making within the Context of Genomic Testing.

Cameron LD, Biesecker BB, Peters E, Taber JM, Klein WMP.

Soc Personal Psychol Compass. 2017 May;11(5). pii: e12315. doi: 10.1111/spc3.12315. Epub 2017 May 5.

32.

Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery.

Shapira R, Turbitt E, Erby LH, Biesecker BB, Klein WMP, Hooker GW.

Fam Cancer. 2018 Oct;17(4):485-493. doi: 10.1007/s10689-017-0065-z.

PMID:
29209897
33.

Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention.

Haakonsen Smith C, Turbitt E, Muschelli J, Leonard L, Lewis KL, Freedman B, Muratori M, Biesecker BB.

J Genet Couns. 2018 Feb;27(1):252-262. doi: 10.1007/s10897-017-0144-1. Epub 2017 Sep 6.

PMID:
28879629
34.

Reactions to clinical reinterpretation of a gene variant by participants in a sequencing study.

Taber JM, Klein WMP, Lewis KL, Johnston JJ, Biesecker LG, Biesecker BB.

Genet Med. 2018 Mar;20(3):337-345. doi: 10.1038/gim.2017.88. Epub 2017 Jul 27.

35.

A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.

Di Gioia SA, Connors S, Matsunami N, Cannavino J, Rose MF, Gilette NM, Artoni P, de Macena Sobreira NL, Chan WM, Webb BD, Robson CD, Cheng L, Van Ryzin C, Ramirez-Martinez A, Mohassel P, Leppert M, Scholand MB, Grunseich C, Ferreira CR, Hartman T, Hayes IM, Morgan T, Markie DM, Fagiolini M, Swift A, Chines PS, Speck-Martins CE, Collins FS, Jabs EW, Bönnemann CG, Olson EN; Moebius Syndrome Research Consortium, Carey JC, Robertson SP, Manoli I, Engle EC.

Nat Commun. 2017 Jul 6;8:16077. doi: 10.1038/ncomms16077.

36.

Widowed parenting self-efficacy scale: A new measure.

Edwards TP, Yopp JM, Park EM, Deal A, Biesecker BB, Rosenstein DL.

Death Stud. 2018 Apr;42(4):247-253. doi: 10.1080/07481187.2017.1339743. Epub 2017 Jul 14.

37.

Personal utility in genomic testing: a systematic literature review.

Kohler JN, Turbitt E, Biesecker BB.

Eur J Hum Genet. 2017 Jun;25(6):662-668. doi: 10.1038/ejhg.2017.10. Epub 2017 Mar 15. Review.

38.

A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling.

Athens BA, Caldwell SL, Umstead KL, Connors PD, Brenna E, Biesecker BB.

J Genet Couns. 2017 Oct;26(5):902-933. doi: 10.1007/s10897-017-0082-y. Epub 2017 Mar 2. Review.

PMID:
28255928
39.

Defining personal utility in genomics: A Delphi study.

Kohler JN, Turbitt E, Lewis KL, Wilfond BS, Jamal L, Peay HL, Biesecker LG, Biesecker BB.

Clin Genet. 2017 Sep;92(3):290-297. doi: 10.1111/cge.12998. Epub 2017 Apr 19.

40.

A taxonomy of medical uncertainties in clinical genome sequencing.

Han PKJ, Umstead KL, Bernhardt BA, Green RC, Joffe S, Koenig B, Krantz I, Waterston LB, Biesecker LG, Biesecker BB.

Genet Med. 2017 Aug;19(8):918-925. doi: 10.1038/gim.2016.212. Epub 2017 Jan 19.

41.

PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing.

Biesecker BB, Woolford SW, Klein WMP, Brothers KB, Umstead KL, Lewis KL, Biesecker LG, Han PKJ.

Clin Genet. 2017 Aug;92(2):172-179. doi: 10.1111/cge.12949. Epub 2017 Jan 30. Erratum in: Clin Genet. 2018 May;93(5):1119.

42.

Engagement and communication among participants in the ClinSeq Genomic Sequencing Study.

Hooker GW, Umstead KL, Lewis KL, Koehly LK, Biesecker LG, Biesecker BB.

Genet Med. 2017 Jan;19(1):98-103. doi: 10.1038/gim.2016.71. Epub 2016 Oct 20.

43.

Family functioning mediates adaptation in caregivers of individuals with Rett syndrome.

Lamb AE, Biesecker BB, Umstead KL, Muratori M, Biesecker LG, Erby LH.

Patient Educ Couns. 2016 Nov;99(11):1873-1879. doi: 10.1016/j.pec.2016.06.018. Epub 2016 Jun 18.

44.

Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age.

Seo J, Ivanovich J, Goodman MS, Biesecker BB, Kaphingst KA.

J Genet Couns. 2017 Jun;26(3):511-521. doi: 10.1007/s10897-016-0006-2. Epub 2016 Aug 20.

45.

Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age.

Elrick A, Ashida S, Ivanovich J, Lyons S, Biesecker BB, Goodman MS, Kaphingst KA.

J Genet Couns. 2017 Feb;26(1):173-181. doi: 10.1007/s10897-016-9995-0. Epub 2016 Jul 16.

46.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium.

Am J Hum Genet. 2016 Jul 7;99(1):246. doi: 10.1016/j.ajhg.2016.06.002. No abstract available.

47.
48.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Green RC, Goddard KAB, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP, Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA, Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM, Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS, Robinson D, Salama JS, Scollon S, Sharp RR, Shirts B, Spinner NB, Tabor HK, Tarczy-Hornoch P, Veenstra DL, Wagle N, Weck K, Wilfond BS, Wilhelmsen K, Wolf SM, Wynn J, Yu JH; CSER Consortium.

Am J Hum Genet. 2016 Jun 2;98(6):1051-1066. doi: 10.1016/j.ajhg.2016.04.011. Epub 2016 May 12. Erratum in: Am J Hum Genet. 2016 Jul 7;99(1):246.

49.

Predictive genetic testing of minors: evidence and experience with families.

Biesecker BB.

Genet Med. 2016 Aug;18(8):763-4. doi: 10.1038/gim.2015.191. Epub 2016 Jan 28. No abstract available.

50.

"Watching time tick by…": Decision making for Duchenne muscular dystrophy trials.

Peay HL, Scharff H, Tibben A, Wilfond B, Bowie J, Johnson J, Nagaraju K, Escolar D, Piacentino J, Biesecker BB.

Contemp Clin Trials. 2016 Jan;46:1-6. doi: 10.1016/j.cct.2015.11.006. Epub 2015 Nov 9.

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