Odgis J, Kelly N, Sebastin M, Golfinopoulos L, Scarimbolo L, Insel B
Public Health Genomics. 2025; 28(1):85-101.
PMID: 39827879
PMC: 11839312.
DOI: 10.1159/000542444.
Clausen M, Krishnapillai S, Hirjikaka D, Kodida R, Shickh S, Reble E
Genet Med Open. 2024; 2:101814.
PMID: 39669596
PMC: 11613922.
DOI: 10.1016/j.gimo.2024.101814.
Scarpa F, Casu M
Int J Environ Res Public Health. 2024; 21(10).
PMID: 39457310
PMC: 11507412.
DOI: 10.3390/ijerph21101337.
Goh E, Chad L, Richer J, Bombard Y, Mighton C, Agatep R
J Med Genet. 2024; 61(12):1123-1131.
PMID: 39362754
PMC: 11672037.
DOI: 10.1136/jmg-2024-110330.
Seed L, Scott A, Pichini A, Peter M, Tadros S, Sortica da Costa C
BMJ Open. 2024; 14(9):e089108.
PMID: 39317512
PMC: 11423729.
DOI: 10.1136/bmjopen-2024-089108.
BRCA genetic testing and counseling in breast cancer: how do we meet our patients' needs?.
Dubsky P, Jackisch C, Im S, Hunt K, Li C, Unger S
NPJ Breast Cancer. 2024; 10(1):77.
PMID: 39237557
PMC: 11377442.
DOI: 10.1038/s41523-024-00686-8.
Factors Associated with Uptake of Patient Portals at a Federally Qualified Health Care Center.
Matthews A, Steffen A, Akufo J, Burke L, Diaz H, Dodd D
Healthcare (Basel). 2024; 12(15).
PMID: 39120208
PMC: 11311389.
DOI: 10.3390/healthcare12151505.
From code to care: Clinician and researcher perspectives on an optimal therapeutic web portal for acute myeloid leukemia.
Knoppers T, Haley C, Bouhouita-Guermech S, Hagan J, Bradbury-Jost J, Alarie S
PLoS One. 2024; 19(4):e0302156.
PMID: 38635542
PMC: 11025855.
DOI: 10.1371/journal.pone.0302156.
The ENGAGE study: a 3-arm randomized hybrid type 1 effectiveness and implementation study of an in-home, collaborative PCP model of remote telegenetic services to increase uptake of cancer genetic services in childhood cancer survivors.
Henderson T, Allen M, Mim R, Egleston B, Fleisher L, Elkin E
BMC Health Serv Res. 2024; 24(1):253.
PMID: 38414045
PMC: 10900774.
DOI: 10.1186/s12913-024-10586-z.
Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol.
Bouffler S, Lee L, Lynch F, Martyn M, Lynch E, Macciocca I
BMJ Open. 2023; 13(6):e072999.
PMID: 37270192
PMC: 10254691.
DOI: 10.1136/bmjopen-2023-072999.
Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review.
Gasteiger N, Vercell A, Khan N, Dowding D, Davies A, Davies A
J Community Genet. 2023; 14(3):227-240.
PMID: 37198378
PMC: 10271952.
DOI: 10.1007/s12687-023-00648-w.
Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?.
White S, Mossfield T, Fleming J, Barlow-Stewart K, Ghedia S, Dickson R
Eur J Hum Genet. 2023; 31(6):703-711.
PMID: 36935418
PMC: 10250371.
DOI: 10.1038/s41431-023-01311-1.
Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
Luca S, Clausen M, Shaw A, Lee W, Krishnapillai S, Adi-Wauran E
Hum Genet. 2023; 142(3):321-330.
PMID: 36629921
PMC: 9838385.
DOI: 10.1007/s00439-022-02512-2.
Digital Health Equity: Addressing Power, Usability, and Trust to Strengthen Health Systems.
Koehle H, Kronk C, Lee Y
Yearb Med Inform. 2022; 31(1):20-32.
PMID: 36463865
PMC: 9719765.
DOI: 10.1055/s-0042-1742512.
From the patient to the population: Use of genomics for population screening.
Mighton C, Shickh S, Aguda V, Krishnapillai S, Adi-Wauran E, Bombard Y
Front Genet. 2022; 13:893832.
PMID: 36353115
PMC: 9637971.
DOI: 10.3389/fgene.2022.893832.
Regulatory oversight and ethical concerns surrounding software as medical device (SaMD) and digital twin technology in healthcare.
Lal A, Dang J, Nabzdyk C, Gajic O, Herasevich V
Ann Transl Med. 2022; 10(18):950.
PMID: 36267783
PMC: 9577733.
DOI: 10.21037/atm-22-4203.
Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.
Leitsalu L, Reigo A, Palover M, Nikopensius T, Lall K, Krebs K
Eur J Hum Genet. 2022; 31(9):1048-1056.
PMID: 36192438
PMC: 10474261.
DOI: 10.1038/s41431-022-01196-6.
Digital health-enabled genomics: Opportunities and challenges.
Bombard Y, Ginsburg G, Sturm A, Zhou A, Lemke A
Am J Hum Genet. 2022; 109(7):1190-1198.
PMID: 35803232
PMC: 9300757.
DOI: 10.1016/j.ajhg.2022.05.001.
Genomics in Egypt: Current Status and Future Aspects.
El-Attar E, Helmy Elkaffas R, Aglan S, Naga I, Nabil A, Abdallah H
Front Genet. 2022; 13:797465.
PMID: 35664315
PMC: 9157251.
DOI: 10.3389/fgene.2022.797465.
ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.
Liles E, Leo M, Freed A, Porter K, Zepp J, Kauffman T
Genet Med. 2022; 24(8):1664-1674.
PMID: 35522237
PMC: 9586129.
DOI: 10.1016/j.gim.2022.04.008.
