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List of works by Beverly M. Yashar

"My Plate is Full": Reasons for Declining a Genetic Evaluation of Hearing Loss.

scientific article published on 4 October 2017

9p partial monosomy and disorders of sex development: review and postulation of a pathogenetic mechanism

scientific article

A Qualitative Study of Anticipated Decision Making around Type 2 Diabetes Genetic Testing: the Role of Scientifically Concordant and Discordant Expectations

scientific article published on 28 July 2016

A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa

scientific article

Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease

scientific article

An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation

scientific article published on 01 August 2006

Association of apolipoprotein E alleles with susceptibility to age-related macular degeneration in a large cohort from a single center

scientific article published in May 2004

Certified Nurse-Midwives' Experiences With Provision of Prenatal Genetic Screening: A Case for Interprofessional Collaboration

scientific article published on 01 October 2019

Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

scientific article (publication date: December 2003)

DNA‐Sequence Patenting: National Society of Genetic Counselors (NSGC) Position Paper

scientific article published on August 1, 2002

Development of a decision support tool in pediatric Differences/Disorders of Sex Development

scientific article published on 13 September 2019

Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs.

scientific article published on April 2011

Does Patient-centered Care Change Genital Surgery Decisions? The Strategic Use of Clinical Uncertainty in Disorders of Sex Development Clinics

scientific article published on 10 October 2018

Ehlers-Danlos syndrome, hypermobility type: A characterization of the patients' lived experience

scientific article published on 6 November 2013

Evaluating and improving the implementation of a community-based hereditary cancer screening program.

scientific article published on 5 March 2018

Expanding the genetic counseling workforce: program directors' views on increasing the size of genetic counseling graduate programs

scientific article

Family communication in a population at risk for hypertrophic cardiomyopathy

scientific article published on 12 October 2014

Family-based exome sequencing identifies rare coding variants in age-related macular degeneration

scientific article published on 03 April 2020

Gender destinies: assigning gender in Disorders of Sex Development-Intersex clinics

scientific article published on 21 June 2019

Genetic testing impacts the utility of prospective familial screening in hypertrophic cardiomyopathy through identification of a nonfamilial subgroup

scientific article published on 22 June 2017

Genetics educational needs in China: physicians' experience and knowledge of genetic testing.

scientific article published on 11 December 2014

Improving access to cancer genetic services: perspectives of high-risk clients in a community-based setting

scientific article published on 24 April 2019

Introduction to the special issue on genetic counseling: a global perspective

scientific article

Meta-analysis of genome scans of age-related macular degeneration

scientific article published on 29 June 2005

Microarray analysis of gene expression in the aging human retina.

scientific article published in August 2002

Molecular testing for hereditary retinal disease as part of clinical care

scientific article published on 01 February 2007

Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene

scientific article (publication date: 24 January 2003)

Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease

scientific article

Non-invasive prenatal screening for trisomy 21: Consumers' perspectives

scientific article published on 09 November 2015

Optimizing efficiency and skill utilization: Analysis of genetic counselors' attitudes regarding delegation in a clinical setting

scientific article published on 13 November 2019

Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis

scientific article published on 19 May 2015

Peering into a Chilean black box: parental storytelling in pediatric genetic counseling

scientific article published on 29 June 2013

Perceptions of licensure: a survey of Michigan genetic counselors

scientific article published on 19 May 2009

Physician Experiences and Understanding of Genomic Sequencing in Oncology.

scientific article published on 24 August 2017

Presented Abstracts from the Thirty Fourth Annual Education Conference of the National Society of Genetic Counselors (Pittsburgh, PA, October 2015).

scientific article published on 24 October 2015

Primary care physicians' understanding and utilization of pediatric exome sequencing results

scientific article published on 30 August 2019

Quality of Life and Autonomy in Emerging Adults with Early‐Onset Neuromuscular Disorders

scientific article published on February 25, 2012

Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15.

scientific article published in October 2002

Rewards and challenges of parenting a child with Down syndrome: a qualitative study of fathers' perceptions

scientific article published on 07 April 2020

The Lived Experience of MRKH: Sharing Health Information with Peers

scientific article published on 7 October 2015

The interface between the practice of medical genetics and human genetic research: what every genetic counselor needs to know

scientific article

Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration

scientific article