Lista de obras -

"It's a Little Different for Men"-Sponsorship and Gender in Academic Medicine: a Qualitative Study

scientific article published on 29 June 2020

A genetic perspective on infant mortality

scientific article published on May 2010

AMEN in challenging conversations: bridging the gaps between faith, hope, and medicine.

artículo científico publicado en 2014

Comparing screening and preventive health behaviors in two study populations: daughters of mothers with breast cancer and women responding to the behavioral risk factor surveillance system survey

artículo científico publicado en 2011

De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease.

artículo científico publicado en 2016

Defining underinsurance among children with special health care needs: a Virginia sample

artículo científico publicado en 2005

Demographic and socioeconomic trends in DNA banking utilization in the USA

artículo científico publicado en 2021

Disparities in the Clinical Encounter: Virginia's African American Children with Special Health Care Needs

artículo científico publicado en 2011

Evidence for a major gene in familial anencephaly

artículo científico publicado en 1990

Evolution of an integrated public health surveillance system.

artículo científico publicado en 2011

Exploring hereditary cancer among dying cancer patients--a cross-sectional study of hereditary risk and perceived awareness of DNA testing and banking.

artículo científico publicado en 2010

Factors Influencing Men's Interest in Gene Testing for Prostate Cancer Susceptibility

artículo científico publicado en 2002

Factors affecting quality of life in children and adolescents with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders

artículo científico publicado en 2019

Family Ties: The Role of Family Context in Family Health History Communication About Cancer

artículo científico publicado en 2016

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

artículo científico publicado en 2009

Gail model risk assessment and risk perceptions

artículo científico publicado en 2004

Genetic Risk, Perceived Risk, and Cancer Worry in Daughters of Breast Cancer Patients ⬇️

artículo científico publicado el 4 de diciembre de 2010

Genetic counselors' current use of personal health records-based family histories in genetic clinics and considerations for their future adoption

artículo científico publicado en 2012

Genetic screening and DNA banking at the end of life #206.

artículo científico publicado en 2011

Genetics assessment at the end of life: suggestions for implementation in clinic and future research

scientific article published on April 2008

Genomics and perinatal care

artículo científico publicado en 2012

Health information technology in screening and treatment of child obesity: a systematic review.

artículo científico

Hereditary renal hypouricemia: a new role for allopurinol?

artículo científico publicado en 2013

Horizontal integration of OMIM across the medical school preclinical curriculum for early reinforcement of clinical genetics principles

artículo científico publicado en 2015

Impact of co-occurring birth defects on the timing of newborn hearing screening and diagnosis

artículo científico publicado en 2011

Implementation and evaluation of the Johns Hopkins University School of Medicine leadership program for women faculty

artículo científico publicado en 2015

Increased risk of birth defects among children from multiple births

artículo científico publicado en 2003

Interdisciplinary research career development: building interdisciplinary research careers in women's health program best practices

artículo científico publicado en 2011

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

artículo científico publicado en 2021

Mammography screening after risk-tailored messages: the women improving screening through education and risk assessment (WISER) randomized, controlled trial

artículo científico publicado en 2009

Mentorship Is Not Enough: Exploring Sponsorship and Its Role in Career Advancement in Academic Medicine

artículo científico publicado en 2019

Milestones for medical students completing a clinical genetics elective.

artículo científico publicado en 2016

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

artículo científico publicado en 2010

Overview: referrals for genetic evaluation from child psychiatrists

artículo científico publicado en 2016

Paternal relatives and family history of breast cancer

artículo científico publicado en 2006

Patient-reported hereditary breast and ovarian cancer in a primary care practice

artículo científico publicado en 2013

PhenX measures for phenotyping rare genetic conditions

artículo científico publicado en 2017

Physicians' current practices and opportunities for DNA banking of dying patients with cancer

artículo científico publicado en 2011

Practical Considerations for Implementing Research Recruitment Etiquette

artículo científico publicado en 2014

Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex

artículo científico publicado en 2010

Recruiting diverse patients to a breast cancer risk communication trial--waiting rooms can improve access.

artículo científico publicado en 2007

Regional models of genetic services in the United States

scientific article published on 06 September 2019

Spiritual coping, family history, and perceived risk for breast cancer--can we make sense of it?

artículo científico publicado en 2006

Talking (or not) about family health history in families of Latino young adults

artículo científico publicado en 2012

The "good planning panel".

artículo científico publicado en 2013

The Five pediatric cancers - update on genetic implications

artículo científico publicado en 2016

The KinFact intervention - a randomized controlled trial to increase family communication about cancer history

artículo científico publicado en 2014

The impact of family history of breast cancer and cancer death on women's mammography practices and beliefs

artículo científico publicado en 2008

The link between providers and patients: how laboratories can ensure quality results with genetic testing

artículo científico publicado en 2003

Tolerance for ambiguity could influence awareness of breast cancer genetic testing and inform health education

artículo científico publicado en 2008

Trends in Unmet Need for Genetic Counseling Among Children With Special Health Care Needs, 2001-2010.

artículo científico publicado en 2015

Underinsurance and key health outcomes for children with special health care needs

artículo científico publicado en 2007

Variations in breast cancer screening and health behaviors by age and race among attendees of women's health clinics

artículo científico publicado en 2009

What women think: cancer causal attributions in a diverse sample of women

artículo científico publicado en 2015

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.

artículo científico publicado en 2016

Youth with special health care needs: transition to adult health care services

artículo científico publicado en 2013

Lista de obras de

"It's a Little Different for Men"-Sponsorship and Gender in Academic Medicine: a Qualitative Study

A genetic perspective on infant mortality

AMEN in challenging conversations: bridging the gaps between faith, hope, and medicine.

Comparing screening and preventive health behaviors in two study populations: daughters of mothers with breast cancer and women responding to the behavioral risk factor surveillance system survey

De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease.

Defining underinsurance among children with special health care needs: a Virginia sample

Demographic and socioeconomic trends in DNA banking utilization in the USA

Disparities in the Clinical Encounter: Virginia's African American Children with Special Health Care Needs

Evidence for a major gene in familial anencephaly

Evolution of an integrated public health surveillance system.

Exploring hereditary cancer among dying cancer patients--a cross-sectional study of hereditary risk and perceived awareness of DNA testing and banking.

Factors Influencing Men's Interest in Gene Testing for Prostate Cancer Susceptibility

Factors affecting quality of life in children and adolescents with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders

Family Ties: The Role of Family Context in Family Health History Communication About Cancer

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Gail model risk assessment and risk perceptions

Genetic Risk, Perceived Risk, and Cancer Worry in Daughters of Breast Cancer Patients ⬇️

Genetic counselors' current use of personal health records-based family histories in genetic clinics and considerations for their future adoption

Genetic screening and DNA banking at the end of life #206.

Genetics assessment at the end of life: suggestions for implementation in clinic and future research

Genomics and perinatal care

Health information technology in screening and treatment of child obesity: a systematic review.

Hereditary renal hypouricemia: a new role for allopurinol?

Horizontal integration of OMIM across the medical school preclinical curriculum for early reinforcement of clinical genetics principles

Impact of co-occurring birth defects on the timing of newborn hearing screening and diagnosis

Implementation and evaluation of the Johns Hopkins University School of Medicine leadership program for women faculty

Increased risk of birth defects among children from multiple births

Interdisciplinary research career development: building interdisciplinary research careers in women's health program best practices

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

Mammography screening after risk-tailored messages: the women improving screening through education and risk assessment (WISER) randomized, controlled trial

Mentorship Is Not Enough: Exploring Sponsorship and Its Role in Career Advancement in Academic Medicine

Milestones for medical students completing a clinical genetics elective.

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

Overview: referrals for genetic evaluation from child psychiatrists

Paternal relatives and family history of breast cancer

Patient-reported hereditary breast and ovarian cancer in a primary care practice

PhenX measures for phenotyping rare genetic conditions

Physicians' current practices and opportunities for DNA banking of dying patients with cancer

Practical Considerations for Implementing Research Recruitment Etiquette

Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex

Recruiting diverse patients to a breast cancer risk communication trial--waiting rooms can improve access.

Regional models of genetic services in the United States

Spiritual coping, family history, and perceived risk for breast cancer--can we make sense of it?

Talking (or not) about family health history in families of Latino young adults

The "good planning panel".

The Five pediatric cancers - update on genetic implications

The KinFact intervention - a randomized controlled trial to increase family communication about cancer history

The impact of family history of breast cancer and cancer death on women's mammography practices and beliefs

The link between providers and patients: how laboratories can ensure quality results with genetic testing

Tolerance for ambiguity could influence awareness of breast cancer genetic testing and inform health education

Trends in Unmet Need for Genetic Counseling Among Children With Special Health Care Needs, 2001-2010.

Underinsurance and key health outcomes for children with special health care needs

Variations in breast cancer screening and health behaviors by age and race among attendees of women's health clinics

What women think: cancer causal attributions in a diverse sample of women

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.

Youth with special health care needs: transition to adult health care services