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Prioritizing Genomic Applications for Action by Level of Evidence: A Horizon-Scanning Method

Clinical pharmacology and therapeutics, 2014-04, Vol.95 (4), p.394-402

2014

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Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles

Gene therapy, 1998, Vol.5 (1), p.19-30

1998

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Polylysine modification of adenoviral fiber protein enhances muscle cell transduction

Human gene therapy, 1999-07, Vol.10 (10), p.1633-1640

1999

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Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectors

Human gene therapy, 1997-03, Vol.8 (4), p.371-380

1997

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The basal lamina is a physical barrier to herpes simplex virus-mediated gene delivery to mature muscle fibers

Journal of Virology, 1996-11, Vol.70 (11), p.8117-8123

1996

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Selection and use of ligands for receptor-mediated gene delivery to myogenic cells

Gene therapy, 1997-07, Vol.4 (7), p.664-674

1997

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A Genetic Test Registry: Bringing Credible and Actionable Data Together

Public health genomics, 2010-01, Vol.13 (6), p.360-361

2010

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Patient Physical Characteristics and Primary Care Physician Decision Making in Preconception Genetic Screening

Public health genomics, 2010-01, Vol.13 (6), p.336-344

2010

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New Standards and Enhanced Utility for Family Health History Information in the Electronic Health Record: An Update from the American Health Information Community's Family Health History Multi-Stakeholder Workgroup

Journal of the American Medical Informatics Association : JAMIA, 2008-11, Vol.15 (6), p.723-728

2008

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Validation of My Family Health Portrait for six common heritable conditions

Genetics in medicine, 2010-06, Vol.12 (6), p.370-375

2010

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Making Personalized Health Care Even More Personalized: Insights From Activities of the IOM Genomics Roundtable

Annals of family medicine, 2015-07, Vol.13 (4), p.373-380

2015

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Molecular genetic and genetic correlations in sodium channelopathies : lack of founder effect and evidence for a second gene

American journal of human genetics, 1993-06, Vol.52 (6), p.1074-1084

1993

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Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families

Neurology, 1993-04, Vol.43 (4), p.668-668

1993

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The economics of genomic medicine: insights from the IOM Roundtable on Translating Genomic-Based Research for Health

JAMA : the journal of the American Medical Association, 2013-03, Vol.309 (12), p.1235

2013

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Hyperkalemic periodic paralysis with cardiac dysrhythmia: A novel sodium channel mutation?

Annals of neurology, 1995-03, Vol.37 (3), p.408-411

1995

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The Genomic Applications in Practice and Prevention Network

Genetics in medicine, 2009-07, Vol.11 (7), p.488-494

2009

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The clinical content of preconception care: women with chronic medical conditions

American journal of obstetrics and gynecology, 2008-12, Vol.199 (6), p.S310-S327

2008

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A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: Recommendations of the United States Secretary for Health and Human Services Advisory Committee on Heritable Disorders in Newborns and Children

Genetics in medicine, 2010-02, Vol.12 (2), p.77-80

2010

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Peas, priorities and primary care: cultural competency starts at home

Genetics in medicine, 2005-10, Vol.7 (8), p.588-589

Feero, W Gregory

2005

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Genetic thrombophilia

Primary Care: Clinics in Office Practice, 2004-09, Vol.31 (3), p.685-709

Feero, W.Gregory

2004

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Their loss is our gain?

Current biology, 1995-01, Vol.5 (11), p.1229-1231

1995

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Selectin and use of ligands for receptor-mediated gene delivery to myogenic cells

Gene therapy, 1997-07, Vol.4 (7), p.664-674

1997

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Huntington's Disease: Their loss is our gain?

Current biology, 1995-11, Vol.5 (11), p.1229-1231

1995

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Identification of a Thr-to-Met Mutation in the Skeletal Muscle Sodium Channel Gene in Hyperkalemic Periodic Paralysis of a Japanese Family

Annals of the New York Academy of Sciences, 1993-12, Vol.707 (1), p.342-345

1993

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Molecular genetic and genetic correlations in sodium channelopathies: Lack of founder effect and evidence for a second gene

American journal of human genetics, 1993-01, Vol.52 (6), p.1073-1084

1993

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Prioritizing Genomic Applications for Action by Level of Evidence: A Horizon-Scanning Method

Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles

Polylysine modification of adenoviral fiber protein enhances muscle cell transduction

Viral gene delivery to skeletal muscle: insights on maturation-dependent loss of fiber infectivity for adenovirus and herpes simplex type 1 viral vectors

The basal lamina is a physical barrier to herpes simplex virus-mediated gene delivery to mature muscle fibers

Selection and use of ligands for receptor-mediated gene delivery to myogenic cells

A Genetic Test Registry: Bringing Credible and Actionable Data Together

Patient Physical Characteristics and Primary Care Physician Decision Making in Preconception Genetic Screening

New Standards and Enhanced Utility for Family Health History Information in the Electronic Health Record: An Update from the American Health Information Community's Family Health History Multi-Stakeholder Workgroup

Validation of My Family Health Portrait for six common heritable conditions

Making Personalized Health Care Even More Personalized: Insights From Activities of the IOM Genomics Roundtable

Molecular genetic and genetic correlations in sodium channelopathies : lack of founder effect and evidence for a second gene

Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families

The economics of genomic medicine: insights from the IOM Roundtable on Translating Genomic-Based Research for Health

Hyperkalemic periodic paralysis with cardiac dysrhythmia: A novel sodium channel mutation?

The Genomic Applications in Practice and Prevention Network

The clinical content of preconception care: women with chronic medical conditions

A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: Recommendations of the United States Secretary for Health and Human Services Advisory Committee on Heritable Disorders in Newborns and Children

Peas, priorities and primary care: cultural competency starts at home

Genetic thrombophilia

Their loss is our gain?

Selectin and use of ligands for receptor-mediated gene delivery to myogenic cells

Huntington's Disease: Their loss is our gain?

Identification of a Thr-to-Met Mutation in the Skeletal Muscle Sodium Channel Gene in Hyperkalemic Periodic Paralysis of a Japanese Family

Molecular genetic and genetic correlations in sodium channelopathies: Lack of founder effect and evidence for a second gene

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