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Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

American journal of human genetics, 2015-07, Vol.97 (1), p.6-21

2015

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The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome)

American journal of medical genetics. Part A, 2009-11, Vol.149A (11), p.2368-2370

2009

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Genetics for the Generalist: Yes, This Is Important for Your Patient

The Medical clinics of North America, 2019-11, Vol.103 (6), p.xvii-xviii

Levy, Howard P., MD, PhD

2019

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Application of a framework to guide genetic testing communication across clinical indications

Genome medicine, 2021-04, Vol.13 (1), p.71-71, Article 71

2021

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A randomized intervention involving family to improve communication in breast cancer care

NPJ breast cancer, 2021-02, Vol.7 (1), p.14-14, Article 14

2021

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Documentation of results and medication prescribing after combinatorial psychiatric pharmacogenetic testing: A case for discrete results

Genetics in medicine, 2024-04, Vol.26 (4), p.101056, Article 101056

2024

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The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results

American journal of human genetics, 2019-04, Vol.104 (4), p.578-595

2019

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Factors associated with adaptation to Klinefelter syndrome: The experience of adolescents and adults

Patient education and counseling, 2015-01, Vol.98 (1), p.90-95

2015

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Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndrome

Autonomic neuroscience, 2020-03, Vol.224, p.102637-102637, Article 102637

2020

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Stickler syndrome: Clinical characteristics and diagnostic criteria

American journal of medical genetics. Part A, 2005-10, Vol.138A (3), p.199-207

2005

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The Impact of Living with Klinefelter Syndrome: A Qualitative Exploration of Adolescents and Adults

Journal of genetic counseling, 2017-08, Vol.26 (4), p.728-737

2017

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Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

Genetics in medicine, 2019-03, Vol.21 (3), p.727-735

2019

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Prevalence and psychosocial correlates of depressive symptoms among adolescents and adults with Klinefelter syndrome

Genetics in medicine, 2011-11, Vol.13 (11), p.966-972

2011

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Physician practices in evaluation and treatment of patients with generalized joint hypermobility and bleeding

Blood coagulation & fibrinolysis, 2021-12, Vol.32 (8), p.591-595

2021

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Sharing in care: engaging care partners in the care and communication of breast cancer patients

Breast cancer research and treatment, 2019-08, Vol.177 (1), p.127-136

2019

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Technical desiderata for the integration of genomic data into Electronic Health Records

Journal of biomedical informatics, 2012-06, Vol.45 (3), p.419-422

2012

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Natural history of aging in Cornelia de Lange syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2007-08, Vol.145C (3), p.248-260

2007

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Characterizing genetic variants for clinical action

American journal of medical genetics. Part C, Seminars in medical genetics, 2014-03, Vol.166C (1), p.93-104

2014

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Thoracolumbar spinal abnormalities in Stickler syndrome

Spine (Philadelphia, Pa. 1976), 2001-02, Vol.26 (4), p.403-409

2001

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Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

American journal of human genetics, 2015-09, Vol.97 (3), p.501-501

2015

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Genetics and Precision Medicine

The Medical clinics of North America, 2019-11, Vol.103 (6), p.i-i

Levy, Howard P.

2019

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Patient reactions to personalized medicine vignettes: An experimental design

Genetics in medicine, 2011-05, Vol.13 (5), p.421-428

2011

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Insomnia in Cornelia de Lange Syndrome

International journal of pediatric otorhinolaryngology, 2012-07, Vol.76 (7), p.972-975

2012

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Characterization of sleep disturbance in Cornelia de Lange Syndrome

International journal of pediatric otorhinolaryngology, 2011-02, Vol.75 (2), p.215-218

2011

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Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm

The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome)

Genetics for the Generalist: Yes, This Is Important for Your Patient

Application of a framework to guide genetic testing communication across clinical indications

A randomized intervention involving family to improve communication in breast cancer care

Documentation of results and medication prescribing after combinatorial psychiatric pharmacogenetic testing: A case for discrete results

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results

Factors associated with adaptation to Klinefelter syndrome: The experience of adolescents and adults

Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndrome

Stickler syndrome: Clinical characteristics and diagnostic criteria

The Impact of Living with Klinefelter Syndrome: A Qualitative Exploration of Adolescents and Adults

Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

Prevalence and psychosocial correlates of depressive symptoms among adolescents and adults with Klinefelter syndrome

Physician practices in evaluation and treatment of patients with generalized joint hypermobility and bleeding

Sharing in care: engaging care partners in the care and communication of breast cancer patients

Technical desiderata for the integration of genomic data into Electronic Health Records

Natural history of aging in Cornelia de Lange syndrome

Characterizing genetic variants for clinical action

Thoracolumbar spinal abnormalities in Stickler syndrome

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

Genetics and Precision Medicine

Patient reactions to personalized medicine vignettes: An experimental design

Insomnia in Cornelia de Lange Syndrome

Characterization of sleep disturbance in Cornelia de Lange Syndrome

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