Sickle cell disease awareness and perception among Christian religious leaders in Accra Metropolis: a qualitative study

2024-10-2

Genetic testing perspectives in Pakistani population: a survey on knowledge, attitudes, awareness, and concerns

2024-10-1

Building a National Policy for Rare Disease in Brazil

2024-9-26

How to communicate and what to disclose to participants in a recall-by-genotype research approach: a multistep empirical study

2024-9-26

Improving the communication of multifactorial cancer risk assessment results for different audiences: a co-design process

2024-9-25

What do women want to see in a personalized breast cancer risk report? A qualitative study of Asian women of two countries

2024-9-25

Research participant perceptions of personal utility in disclosure of individual research results from genomic analysis

2024-9-18

The mentee report: outcomes from implementing a mentorship program for international genetic counseling applicants

2024-9-9

Raising awareness and education of genetic testing and counseling through fotonovelas among Latina women at risk for hereditary breast and ovarian cancer

2024-9-6

From stigma to increased social acceptance? Living with Machado-Joseph disease in São Miguel, Azores, Portugal

2024-8-31

Deciphering the needs of patients with hereditary breast and ovarian Cancer in the Process of Genetic Counseling to Inform the Development of a Mobile Support App: a qualitative study in Germany

2024-8-19

The importance of geographic and sociodemographic aspects in the characterization of mucopolysaccharidoses: a case series from Ceará state (Northeast Brazil)

2024-8-19

Teaching and training of human resources for genetics and genomics in Brazil

2024-8-13

Barriers, motivators and strategies to increase participation in genetic research among Asian and Black families of autistic individuals

2024-8-13

“I don’t think people should die young”: perspectives of parents with children diagnosed with familial hypercholesterolemia

2024-8-10

Knowledge, attitudes, and practices of primary healthcare practitioners in low- and middle-income countries: a scoping review on genetics

2024-8-9

Parental perspectives regarding the return of genomic research results in neurodevelopmental disorders in South Africa: anticipated impact and preferences

2024-8-2

Is Tunisia ready for precision medicine? Challenges of medical genomics within a LMIC healthcare system

2024-7-31

Exploring family communication preferences in hereditary breast and ovarian cancer and Lynch syndrome: a national Canadian survey

2024-7-24

“Living with a question mark”: psychosocial experience of Portuguese young adults at risk for hereditary amyloid transthyretin amyloidosis with polyneuropathy

2024-7-8

Congenital anomalies in Santa Catarina, Southern Brazil: macroregional and temporal birth prevalence for the period 2011–2020

2024-6-25

“Unnatural resources?”: parallels and distinctions between the Newfoundland Genome and traditional resource sectors

2024-6-19

Knowledge of genetics and attitudes toward genetic testing among university students in Indonesia

2024-6-8

Prevalence of congenital anomalies and prenatal diagnosis by birth institution (public vs. non-public): indicators of inequality in access to elective termination of pregnancy for fetal anomalies

2024-6-1

Family communication of cancer genetic test results in an ethnically diverse population: a qualitative exploration of more than 200 patients

2024-5-30

Health-related roles of older generations in families with inherited genetic conditions: a scoping review

2024-5-25

Caregiver-reported barriers to care for children and adults with Williams Syndrome

2024-5-22

The acceptability and clinical impact of using polygenic scores for risk-estimation of common cancers in primary care: a systematic review

2024-5-21

The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis

2024-5-10

The need to set explicit goals for human germline gene editing public dialogues

2024-5-8

Comparative assessment of quality of life among adolescents with sickle cell disease and sickle cell trait: evidence from Odisha, India

2024-4-8

Patient perspectives on pharmacogenomic (PGx) testing for antidepressant prescribing in primary care: a qualitative description study

2024-4-8

A collaborative model for Medical Genetics services delivery in Portugal: a multidisciplinary perspective

2024-3-7

Research biobank participants attitudes towards genetic exceptionalism and health record confidentiality

2024-3-5

The urgency for a change in genetics healthcare provision: views from Portuguese medical geneticists

2024-3-1

Understanding perceptions of tumor genomic profile testing in Black/African American cancer patients in a qualitative study: the role of medical mistrust, provider communication, and family support

2024-2-16

Public participation in human genome editing research governance: what do scientists think?

2024-2-14

Development of a culturally targeted chatbot to inform living kidney donor candidates of African ancestry about APOL1 genetic testing: a mixed methods study

2024-2-13

Endline assessment of knowledge about sickle cell disease among the tribal community of Chhotaudepur district of Gujarat

2024-2-9

Attitudes of medical professionals toward fragile X carrier screening and genetic counseling in China

2024-1-26

Advertisement by medical facilities as an opportunity route of APOE genetic testing in Japan: a website analysis

2024-1-15

Empowerment of genetic information by women at-risk of being carriers of Duchenne and Becker muscular dystrophies

2024-1-2

Wikipedia as an academic service-learning tool in science and technology: higher education case from Siberia

2023-12-21

Training of community health agents — a strategy for earlier recognition of mucopolysaccharidoses

2023-12-20

Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population

2023-12-20

Patient experiences in receiving telegenetics care for inherited cardiovascular diseases

2023-12-14

A qualitative exploration of interprofessional collaborative practice between genetic counselors and mental health providers

2023-12-8

Latina immigrants’ breast and colon cancer causal attributions: genetics is key

2023-11-30

Survey of attitude to human genome modification in Nigeria

2023-11-23

Genetic risk prediction in Hispanics/Latinos: milestones, challenges, and social-ethical considerations

2023-11-14