Genetic services survey—experience of people with rare diseases and their families accessing genetic services in the Irish Republic AJ WardDM LambertSA Lynch Research Open access 26 August 2023 Pages: 583 - 592
Quality of life of Brazilian families who have children with Fragile X syndrome: a descriptive study Thamires Rosa dos SantosNicoly Stefani Sevalho CarlucciDébora Gusmão Melo Research 18 August 2023 Pages: 407 - 418
Psychosocial impacts of caring for a child with a genetic disorder in Accra, Ghana Paul OpokuAnnabella Osei-TutuMabel Oti-Boadi Research 15 August 2023 Pages: 565 - 574
Genetic counseling in sickle cell disease: Insights from the Indian tribal population Pooja AggarwalDeepa Bhat Review 04 August 2023 Pages: 345 - 353
Identification of maternal attitudes and knowledge about newborn screenings: a Turkey sample Türkan KadiroğluGamzegül AltayÇiğdem Can Bayrak Research 03 August 2023 Pages: 555 - 564
Nigerian parents’ perspectives on genetic testing in their children with genetic eye diseases Henrietta Ifechukwude MonyeOlusola Oluyinka OlawoyeTunji Sunday Oluleye Research 27 July 2023 Pages: 387 - 394
A pilot evaluation of an 8-week mindfulness-based stress reduction program for people with pre-symptomatic Huntington’s disease Sarah VelissarisMarie-Claire DavisJulie C. Stout Research 17 July 2023 Pages: 395 - 405
Adolescents’ experiences and views of the national school-based thalassaemia screening programme in Malaysia: a qualitative study Huey Yee TanNorita HusseinTun Firzara Abdul Malik Research 01 July 2023 Pages: 361 - 369
The beta thalassaemia trait in Jamaica G. R. SerjeantB. E. SerjeantA. E. Kulozik Research 30 June 2023 Pages: 355 - 360
“What if” should precede “whether” and “how” in the social conversation around human germline gene editing Diewertje HoutmanWendy GeuverinkSam Riedijk Research Open access 16 June 2023 Pages: 371 - 375
The role of polygenic risk scores in breast cancer risk perception and decision-making Leslie RiddleGalen JosephJennifer Elyse James Research Open access 13 June 2023 Pages: 489 - 501
Life story of Iranian parents of a child with phenylketonuria: a qualitative study Marjan Mardani-HamoolehHaydeh Heidari Research 06 June 2023 Pages: 419 - 427
“Fruits of our past karma”: a qualitative study on knowledge and attitudes about congenital anomalies among women in Pune district, India Anita KarDipali DhamdhereAishwarya Medhekar Research 03 June 2023 Pages: 429 - 438
Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review Norina GasteigerAmy VercellAlan Davies Review Open access 18 May 2023 Pages: 227 - 240
The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation Aaliyah HeywardKelsi HagertyNandini Govil Research 08 May 2023 Pages: 377 - 385
Knowledge, attitude, and perceptions about cancer genetic testing in clinical practice in Karachi, Pakistan Shameel ShafqatMasooma NaseemZahid Mehmood Research 05 May 2023 Pages: 337 - 344
Clinical utility of polygenic risk scores: a critical 2023 appraisal Sebastian KochJörg SchmidtkeAmke Caliebe Research Open access 03 May 2023 Pages: 471 - 487
Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project Sonia OkuyamaLarissa L. WhiteHeather Spencer Feigelson Research Open access 01 May 2023 Pages: 329 - 336
A review of key terminology and definitions used for birth defects globally HL MalherbeB Modell C Aldous Research Open access 24 April 2023 Pages: 241 - 262
Never “totally prepared”: Support groups on helping families prepare for a child with a genetic condition Kaitlynn P. CraigKirsten A. RigganMarsha Michie Research 12 April 2023 Pages: 319 - 327
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study Laura WeddMargaret GleesonRajneesh Kaur Research Open access 03 April 2023 Pages: 307 - 317
Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community Inez BeadellMalia ByunStephanie Best Research Open access 31 March 2023 Pages: 295 - 305
Communicating risk and the landscape of cancer prevention — an exploratory study that examines perceptions of cancer-related genetic counseling and testing among African Americans and Latinos in the Midwest Crystal Y. LumpkinsRafaela NelsonAndrew K. Godwin Original Article Open access 17 March 2023 Pages: 121 - 133
An exemplary model of genetic counselling for highly specialised services Juliette HarrisMarion BartlettFleur S van Dijk Review 09 March 2023 Pages: 115 - 119
Fundamental knowledge taught in compulsory education for effective genetic counseling: a qualitative study of descriptions in textbooks Eri SakaiTakahiro YamadaShinji Kosugi Research 28 February 2023 Pages: 263 - 274
Pakistani healthcare professionals’ perceptions of communication with patients and their relatives about hereditary breast cancer: a qualitative study in a LMIC Shenaz AhmedHussain JafriMushtaq Ahmed Research Open access 23 February 2023 Pages: 287 - 294
Re-envisioning community genetics: community empowerment in preventive genomics Hannah WandDaphne O. Martschenkoon behalf of the Preventive Genomics Program Co-Design Working Group Research 11 February 2023 Pages: 459 - 469
New year, new goals for the journal? Martina C. CornelAngus Clarke Editorial 11 February 2023 Pages: 1 - 3
Correction to: Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling Colleen JodarskiRylee DuncanMorgan Similuk Correction Open access 10 February 2023 Pages: 27 - 27
What makes a good life: using theatrical performance to enhance communication about polygenic risk scores research in patient and public involvement Amy M. MasonIfunanya ObiSarah Fahle Research Open access 10 February 2023 Pages: 453 - 458
Interventions addressing genetic disease burdens within selected countries in the MENA region: a scoping review Madison GrantTamar Kabakian-KhasholianSoha Yazbek Review 24 January 2023 Pages: 29 - 39
Public’s awareness of biobanks and willingness to participate in biobanking: the moderating role of social value orientation Matúš GrežoMartin Sedlár Research 20 January 2023 Pages: 275 - 285
Health in Our Hands: diabetes and substance use education through a new genomic framework for schools and communities Stephen M. ModellIrene S. BayerElla Greene-Moton Research Open access 16 January 2023 Pages: 211 - 225
Assessing patient-level knowledge of precision medicine in a community health center setting Sarah C. StallingsJennifer RichmondMelinda C. Aldrich Research 07 January 2023 Pages: 197 - 210
Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling Colleen JodarskiRylee DuncanMorgan Similuk Review Open access 07 January 2023 Pages: 17 - 25
Mothers of children with Down syndrome: a clinical and epidemiological study Joissy AprigioCarolina M. L. de CastroMárcia R. Amorim Research 23 December 2022 Pages: 189 - 195
Evaluating visual imagery for participant understanding of research concepts in genomics research Erin RothwellNaomi O. RichesJoshua L. Bonkowsky Original Article 19 December 2022 Pages: 51 - 62
Ethical, legal, and social implications of genetic risk prediction for multifactorial disease: a narrative review identifying concerns about interpretation and use of polygenic scores Carolyn Riley Chapman Research 19 December 2022 Pages: 441 - 452
Understanding how educational interventions improve treatment adherence in patients with familial hypercholesterolaemia: a systematic review Hannah MasseyBarbara JenningsZosia Miedzybrodzka Review 13 December 2022 Pages: 5 - 15
Lost in print: difficulty in reading online information pertaining to phenylketonuria Lalitha SamuelJoseph FeraCorey H. Basch Research 11 December 2022 Pages: 185 - 188
Identification of psychoeducation needs and an intervention response for pre-symptomatic Huntington’s disease Cathy GluyasLisa MottramJulie Stout Research 10 December 2022 Pages: 175 - 183
Human genetics education as part of the Japanese Cancer Education Comprehensive Support Project Fumi Yamada-KurebayashiMotoko SasakiHidehiko Miyake Research 30 November 2022 Pages: 163 - 174
Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK Alison C. KayNicola V. Taverner Research Open access 29 November 2022 Pages: 149 - 162
Cost-effectiveness of a gene sequencing test for Alzheimer’s disease in Ontario Nicolas IragorriDanielle ToccalinoThe ONDRI Investigators Research 25 November 2022 Pages: 135 - 147
Service provision of genetics health care in Portugal C. CostaM. S. LemosM. Paneque Research 22 November 2022 Pages: 101 - 113
Telehealth in genetic counselling consultations: the impact of COVID-19 in a Portuguese genetic healthcare service Mayla A. A. DantasJorge Diogo Da SilvaMilena Paneque Research 22 November 2022 Pages: 91 - 100
Cross-sectional survey on genetic testing utilization and perceptions in Wisconsin Amish and Mennonite communities Katie B. WilliamsMichael R. LasarevChristine M. Seroogy Original Article 17 November 2022 Pages: 41 - 49
Ophthalmic genetic counselling: emerging trends in practice perspectives in Asia Esther K. Y. HuiJason C. S. YamGovindasamy Kumaramanickavel Research 02 November 2022 Pages: 81 - 89
Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: a web-based panel discussion Myla AshfaqSyed A. AhmedAisha Furqan Research 20 October 2022 Pages: 71 - 80
Direct-to-consumer genetic testing in the news: a descriptive analysis Corey H. BaschGrace C. HillyerBetty Cohn Research 14 October 2022 Pages: 63 - 69