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Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas

Journal of genetic counseling, 2020-08, Vol.29 (4), p.530-541

2020

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Patients with unexplained mismatch repair deficiency are interested in updated genetic testing

Hereditary cancer in clinical practice, 2020-09, Vol.18 (1), p.19-19, Article 19

2020

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Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications

Journal of genetic counseling, 2019-06, Vol.28 (3), p.692-699

2019

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Survival of Texas infants born with trisomies 21, 18, and 13

American journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.360-366

2010

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First Neonatal Demise with Travel-Associated Zika Virus Infection in the United States of America

American journal of perinatology reports, 2017-04, Vol.7 (2), p.e68-e73

2017

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Indications for genetic referral: a guide for healthcare providers

Genetics in medicine, 2007-06, Vol.9 (6), p.385-389

2007

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Perceptions of Latinas on the Traditional Prenatal Genetic Counseling Model

Journal of genetic counseling, 2015-08, Vol.24 (4), p.675-682

2015

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The psychosocial effects of the Li-Fraumeni Education and Early Detection (LEAD) program on individuals with Li-Fraumeni syndrome

Genetics in medicine, 2017-09, Vol.19 (9), p.1064-1070

2017

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Fetal trisomy 21 and the risk of preeclampsia

The journal of maternal-fetal & neonatal medicine, 2010-01, Vol.23 (1), p.55-59

2010

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Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices

Journal of genetic counseling, 2020-10, Vol.29 (5), p.728-736

2020

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eP303: A tale of two tests: A PGT-M and expanded carrier screening clinical experience study

Genetics in medicine, 2022-03, Vol.24 (3), p.S192-S193

2022

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Knowledge and Self-Esteem of Individuals with Neurofibromatosis Type 1 (NF1)

Journal of genetic counseling, 2017-06, Vol.26 (3), p.620-627

2017

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The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers

Prenatal diagnosis, 2019-04, Vol.39 (5), p.351-360

2019

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Evaluating the NCCN Clinical Criteria for Recommending BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer

Journal of the National Comprehensive Cancer Network, 2017-06, Vol.15 (6), p.797

2017

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Undergraduate Student Perceptions and Awareness of Genetic Counseling

Journal of genetic counseling, 2019-02, Vol.28 (1), p.27-39

2019

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Genetic Testing Practices of Genetic Counselors, Geneticists, and Pediatric Neurologists With Regard to Childhood-Onset Neurogenetic Conditions

Journal of child neurology, 2019-03, Vol.34 (4), p.177-183

2019

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A patient with isochromosome 18q, radial‐thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation

American journal of medical genetics, 2005-02, Vol.133A (1), p.93-98

2005

Volltextzugriff (PDF)

Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States

Journal of genetic counseling, 2017-10, Vol.26 (5), p.1041-1058

2017

Volltextzugriff (PDF)

2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling

Journal of genetic counseling, 2016-10, Vol.25 (5), p.868-879

2016

Volltextzugriff (PDF)

Is it all Lynch syndrome?: An assessment of family history in individuals with mismatch repair-deficient tumors

Genetics in medicine, 2015-06, Vol.17 (6), p.476-484

2015

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Exploring the Role of Religiosity and Spirituality in Amniocentesis Decision-Making Among Latinas

Journal of genetic counseling, 2011-12, Vol.20 (6), p.660-673

2011

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National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions

Journal of genetic counseling, 2018-02, Vol.27 (1), p.9-15

2018

Volltextzugriff (PDF)

Influence of Anchoring on Miscarriage Risk Perception Associated with Amniocentesis

Journal of genetic counseling, 2015-04, Vol.24 (2), p.278-284

2015

Volltextzugriff (PDF)

Fetal trisomy 21 and the risk of preeclampsia

The journal of maternal-fetal & neonatal medicine, 2009, p.1-5

2009

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Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents

Genetics in medicine, 2009-03, Vol.11 (3), p.163-168

2009

Volltextzugriff (PDF)

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Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas

Patients with unexplained mismatch repair deficiency are interested in updated genetic testing

Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications

Survival of Texas infants born with trisomies 21, 18, and 13

First Neonatal Demise with Travel-Associated Zika Virus Infection in the United States of America

Indications for genetic referral: a guide for healthcare providers

Perceptions of Latinas on the Traditional Prenatal Genetic Counseling Model

The psychosocial effects of the Li-Fraumeni Education and Early Detection (LEAD) program on individuals with Li-Fraumeni syndrome

Fetal trisomy 21 and the risk of preeclampsia

Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices

eP303: A tale of two tests: A PGT-M and expanded carrier screening clinical experience study

Knowledge and Self-Esteem of Individuals with Neurofibromatosis Type 1 (NF1)

The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers

Evaluating the NCCN Clinical Criteria for Recommending BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer

Undergraduate Student Perceptions and Awareness of Genetic Counseling

Genetic Testing Practices of Genetic Counselors, Geneticists, and Pediatric Neurologists With Regard to Childhood-Onset Neurogenetic Conditions

A patient with isochromosome 18q, radial‐thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation

Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States

2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling

Is it all Lynch syndrome?: An assessment of family history in individuals with mismatch repair-deficient tumors

Exploring the Role of Religiosity and Spirituality in Amniocentesis Decision-Making Among Latinas

National Society of Genetic Counselors Code of Ethics: Explication of 2017 Revisions

Influence of Anchoring on Miscarriage Risk Perception Associated with Amniocentesis

Fetal trisomy 21 and the risk of preeclampsia

Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents

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