B. Yashar

发表

Stimulatory effects of yeast and mammalian 14-3-3 proteins on the Raf protein kinase.

K. Irie, K. Matsumoto, B. Errede, 1994, Science.

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

B. Yashar, Jing Li, Tengda Xu, 2014, Genetics in Medicine.

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

M. Smith-Wheelock, A. Swaroop, S. Zareparsi, 2004, Investigative ophthalmology & visual science.

The introduction of genetic counseling in Ethiopia: Results of a training workshop and lessons learned

B. Yashar, Betregiorgis Hailu Zegeye, Bridget C. O’Connor, 2021, PloS one.

Evaluation of the ELOVL4 gene in patients with age-related macular degeneration

P. Sieving, A. Hutchinson, A. Swaroop, 2001, Ophthalmic genetics.

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

B. Yashar, S. Greenberg, M. Marvin, 2019, Journal of Community Genetics.

Certified Nurse-Midwives' Experiences With Provision of Prenatal Genetic Screening

B. Yashar, R. Zielinski, Shenin A. Dettwyler, 2019, The Journal of perinatal & neonatal nursing.

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

J. Roberts, B. Yashar, K. Christensen, 2011, Genetics in Medicine.

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

B. Yashar, Bridget C. O’Connor, Sarah Mazzola, 2019, Journal of genetic counseling.

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

B. Yashar, T. Jayaratne, Emily J. Moe, 2017, Journal of Genetic Counseling.

Searching for Answers: Information-Seeking by Young People At-Risk for Huntington’s Disease

R. Albin, B. Yashar, W. Uhlmann, 2022, Journal of Huntington's disease.

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

G. Abecasis, J. Haines, M. Pericak-Vance, 2005, Human molecular genetics.

Novel members of the mitogen-activated protein kinase activator family in Xenopus laevis

L. Zon, B. Errede, B. Yashar, 1993, Molecular and cellular biology.

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

L. Siminoff, S. Timmermans, E. Vilain, 2019, Sociology of health & illness.

Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations

Lynette Hammond Gerido, J. Griggs, K. Resnicow, 2022, Journal of genetic counseling.

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

B. Yashar, D. Clauw, W. Uhlmann, 2013, American journal of medical genetics. Part A.

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

B. Yashar, M. Marvin, L. Robinson, 2019, Journal of genetic counseling.

Assessing the impact of pre‐test education on patient knowledge, perceptions, and expectations of pharmacogenomic testing to guide antidepressant use

B. Yashar, Nicholette T. Sloat, V. Ellingrod, 2022, Journal of genetic counseling.

Dynamics and organization of MAP kinase signal pathways

K. Irie, B. Errede, D. E. Levin, 1995, Molecular reproduction and development.

“My Plate is Full”: Reasons for Declining a Genetic Evaluation of Hearing Loss

B. Yashar, M. Lesperance, Tori L. Melendez, 2018, Journal of Genetic Counseling.

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

B. Yashar, K. Owens, L. Kiedrowski, 2016, Journal of Genetic Counseling.

Changes in polyadenylated RNA sequences associated with fruiting body morphogenesis in Coprinus cinereus

B. Yashar, P. Pukkila, 1985 .

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

J. Dowling, E. Petty, B. Yashar, 2012, Journal of Genetic Counseling.

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

L. Siminoff, S. Timmermans, E. Vilain, 2018, Journal of health and social behavior.

Analysis of meiotic development in Coprinus cinereus.

B. Yashar, P. Pukkila, D. Binninger, 1984, Symposia of the Society for Experimental Biology.

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

G. Abecasis, Mingyao Li, A. Swaroop, 2005, Human molecular genetics.

Toll-like receptor 4 variant D 299 G is associated with susceptibility to age-related macular degeneration

G. Abecasis, Mingyao Li, A. Swaroop, 2005 .

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

T. Glover, B. Yashar, C. Keegan, 2013, American journal of medical genetics. Part A.

Microarray analysis of gene expression in the aging human retina.

A. Swaroop, S. Yoshida, B. Yashar, 2002, Investigative ophthalmology & visual science.

Molecular Genetic Diagnosis of Inherited Cancer Predisposition

E. Petty, B. Yashar, 2002 .

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

B. Yashar, S. Day, P. Arscott, 2017, Genetics in Medicine.

A guide to genetic counseling

B. Yashar, W. Uhlmann, Jane L. Schuette, 1998 .

Improving gender‐affirming care in genetic counseling: Using educational tools that amplify transgender and/or gender non‐binary community voices

B. Yashar, Diane R. Koeller, Bailey Hulswit, 2022, Journal of genetic counseling.

Continuing a search for a diagnosis: the impact of adolescence and family dynamics

William E. Byrd, Marni J. Falk, Mahshid S. Azamian, 2023, Orphanet Journal of Rare Diseases.

Physician Experiences and Understanding of Genomic Sequencing in Oncology

A. Chinnaiyan, B. Zikmund‐Fisher, B. Yashar, 2018, Journal of Genetic Counseling.

Family Communication in a Population at Risk for Hypertrophic Cardiomyopathy

L. Salberg, B. Yashar, S. Day, 2015, Journal of Genetic Counseling.

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

L. Siminoff, S. Timmermans, E. Vilain, 2019, Seminars in pediatric surgery.

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

P. Sieving, S. Jacobson, A. Swaroop, 2002, American journal of human genetics.

The Lived Experience of MRKH: Sharing Health Information with Peers.

B. Yashar, C. Keegan, A. Lossie, 2016, Journal of pediatric and adolescent gynecology.

Disclosure of genetic risk to dating partners among young adults with von Hippel-Lindau disease.

B. Yashar, M. Marvin, T. Else, 2022, Familial cancer.

Yeast MEK-dependent signal transduction: response thresholds and parameters affecting fidelity

Brian J. Stevenson, K. Irie, K. Matsumoto, 1995, Molecular and cellular biology.

Shigeo Yoshida, Anand Swaroop, Gonçalo R Abecasis, 2004, American journal of human genetics.

G. Abecasis, P. Sieving, S. Jacobson, 2004 .

Molecular testing for hereditary retinal disease as part of clinical care.

P. Sieving, J. Heckenlively, K. Branham, 2007, Archives of ophthalmology.

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

B. Yashar, R. Molday, M. Mura, 2006, Vision Research.

Searching for Genotype-Phenotype Correlations in X-Linked Juvenile Retinoschisis

P. Sieving, B. Yashar, R. Ayyagari, 2001 .

Juvenile retinoschisis: a model for molecular diagnostic testing of X-linked ophthalmic disease.

P. Sieving, B. Yashar, R. Ayyagari, 1999, Transactions of the American Ophthalmological Society.

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

B. Yashar, Rachel Pothast, C. Wicklund, 2016, Genetics in Medicine.

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

A. Milam, G. Aguirre, A. Swaroop, 2002, Experimental eye research.

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

P. Sieving, S. Schwartz, S. Jacobson, 2012, Investigative ophthalmology & visual science.

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

A. Swaroop, D. Breuer, B. Yashar, 2003, Ophthalmic genetics.

X-Linked Retinitis Pigmentosa: Current Status

P. Sieving, S. Jacobson, A. Swaroop, 2001 .

A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination

M. Myers, B. Yashar, Laura Conway, 2021, Journal of genetic counseling.

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

Alan M. Kwong, G. Abecasis, E. Chew, 2020, Human molecular genetics.

Peering into a Chilean Black Box: Parental Storytelling in Pediatric Genetic Counseling

B. Yashar, Katy Downs, J. Ordóñez, 2013, Journal of Genetic Counseling.

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

B. Zikmund‐Fisher, B. Yashar, Jane P. Sheldon, 2016, American journal of medical genetics. Part A.

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change

P. Sieving, G. Fishman, B. Yashar, 1999, Human mutation.

The Interface Between the Practice of Medical Genetics and Human Genetic Research: What Every Genetic Counselor Needs to Know

B. Yashar, D. Markel, 2004, Journal of Genetic Counseling.

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

B. Yashar, M. Oliver, Jane P. Sheldon, 2020, Disability and rehabilitation.

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

B. Yashar, Kelly J. Branda, K. Taylor, 2002, Journal of Genetic Counseling.

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

B. Yashar, S. Greenberg, M. Marvin, 2018, Journal of Community Genetics.

Graduate training during the COVID‐19 pandemic: North American genetic counseling students' challenges, intolerance of uncertainty, and psychological well‐being

B. Yashar, Jane P. Sheldon, A. Carmichael, 2021, Journal of genetic counseling.

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

P. Sieving, S. Jacobson, A. Swaroop, 2003, Molecular vision.

Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.

P. Sieving, A. Swaroop, A. Wright, 2000, American journal of human genetics.

Perceptions of Licensure: A Survey of Michigan Genetic Counselors

A. Trepanier, L. Rozek, B. Yashar, 2009, Journal of Genetic Counseling.

Introduction to the Special Issue on Genetic Counseling: A Global Perspective

B. Yashar, M. Peterson, 2013, Journal of Genetic Counseling.

Preadoption Genetic Testing: Social workers' decision-making process

B. Yashar, W. Uhlmann, K. Freeark, 2018, Adoption Quarterly.

Providing comprehensive genetic‐based ophthalmic care

B. Yashar, K. Branham, B M Yashar, 2013, Clinical genetics.

Presented Abstracts from the Thirty Third Annual Education Conference of the National Society of Genetic Counselors (New Orleans, LA, September 2014)

B. Yashar, Emily Edelman, Katie Darin, 2014, Journal of Genetic Counseling.

Remapping of the RP 15 Locus for X-Linked Cone-Rod Degeneration to Xp 11 . 4p 21 . 1 , and Identification of a De Novo Insertion in the RPGR Exon ORF 15

P. Sieving, A. Swaroop, R. Vervoort, 2022 .

Learning from our patients: Utilizing the expertise of transgender and/or gender diverse educators to build an inclusive learning cycle

B. Yashar, Bailey Hulswit, Nicole Huser, 2023, Journal of genetic counseling.