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Invited commentary: The Covid-19 pandemic in the United States

International journal for equity in health, 2021-01, Vol.20 (1), p.3-3, Article 3

Holtzman, Neil A Tony

2021

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Editorial Commentary on “Psychological Impact of Learning CDKN2A Variant Status as a Genetic Research Result” by Zhu et al

Public health genomics, 2018-01, Vol.21 (3/4), p.164-167

2018

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ACMG recommendations on incidental findings are flawed scientifically and ethically

Genetics in medicine, 2013-09, Vol.15 (9), p.750-751

Holtzman, Neil A.

2013

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Data withholding in genetics and the other life sciences: prevalences and predictors

Academic medicine, 2006-02, Vol.81 (2), p.137-145

2006

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The strange malady of Alessandro's uncle

BMJ, 2007-12, Vol.335 (7633), p.1306-1307

Holtzman, Neil A Tony

International edition, 2007

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Newborn screening for severe combined immunodeficiency: progress and challenges

JAMA : the journal of the American Medical Association, 2014-08, Vol.312 (7), p.701

Holtzman, Neil A

2014

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Will Genetics Revolutionize Medicine?

The New England journal of medicine, 2000-07, Vol.343 (2), p.141-144

2000

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Promoting Safe and Effective Genetic Tests in the United States: Work of the Task Force on Genetic Testing

Clinical chemistry (Baltimore, Md.), 1999-05, Vol.45 (5), p.732-738

Holtzman, Neil A

1999

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Data withholding in academic genetics: evidence from a national survey

JAMA : the journal of the American Medical Association, 2002-01, Vol.287 (4), p.473

2002

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Withdrawing FDA approval of midodrine after marketing

JAMA : the journal of the American Medical Association, 2011-02, Vol.305 (8), p.781

2011

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The evidence dilemma and cultural change

Health Affairs, 2009-05, Vol.28 (3), p.925-926

Holtzman, Neil A

2009

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How does the mode of inheritance of a genetic condition influence families? A study of guilt, blame, stigma, and understanding of inheritance and reproductive risks in families with X-linked and autosomal recessive diseases

Genetics in medicine, 2006-04, Vol.8 (4), p.234-242

2006

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Expanding newborn screening: how good is the evidence?

JAMA : the journal of the American Medical Association, 2003-11, Vol.290 (19), p.2606

Holtzman, Neil A

2003

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The media and public reaction to genetic research

JAMA : the journal of the American Medical Association, 2002-02, Vol.287 (6), p.773

2002

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What Role for Public Health in Genetics and Vice Versa?

Community genetics, 2006-01, Vol.9 (1), p.8-20

Holtzman, Neil A.

2006

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Management of hyperbilirubinemia: quality of evidence and cost

Pediatrics (Evanston), 2004-10, Vol.114 (4), p.1086-1088

Holtzman, Neil A

2004

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Are Genetic Tests Adequately Regulated?

Science (American Association for the Advancement of Science), 1999-10, Vol.286 (5439), p.409-409

Holtzman, Neil A.

1999

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The new genetics: Genetic testing and public policy

BMJ, 1998-03, Vol.316 (7134), p.852-856

1998

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Does knowledge about the genetics of breast cancer differ between nongeneticist physicians who do or do not discuss or order BRCA testing?

Genetics in medicine, 2003-03, Vol.5 (2), p.99-105

2003

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Scientists' and science writers' experiences reporting genetic discoveries: Toward an ethic of trust in science journalism

Genetics in medicine, 2005-03, Vol.7 (3), p.198-205

2005

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Mapping the human genome: An assessment of media coverage and public reaction

Genetics in medicine, 2002-01, Vol.4 (1), p.31-36

2002

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The Quality of Media Reports on Discoveries Related to Human Genetic Diseases

Community genetics, 2005-01, Vol.8 (3), p.133-144

2005

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Adoption of Liquid-Based Cervical Cancer Screening Tests by Family Physicians and Gynecologists

Health services research, 2004-08, Vol.39 (4p1), p.927-948

2004

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PUTTING THE SEARCH FOR GENES IN PERSPECTIVE

International journal of health services, 2001-01, Vol.31 (2), p.445-461

Holtzman, Neil A.

2001

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Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease

American journal of medical genetics, 2003-05, Vol.119C (1), p.60-69

2003

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Invited commentary: The Covid-19 pandemic in the United States

Editorial Commentary on “Psychological Impact of Learning CDKN2A Variant Status as a Genetic Research Result” by Zhu et al

ACMG recommendations on incidental findings are flawed scientifically and ethically

Data withholding in genetics and the other life sciences: prevalences and predictors

The strange malady of Alessandro's uncle

Newborn screening for severe combined immunodeficiency: progress and challenges

Will Genetics Revolutionize Medicine?

Promoting Safe and Effective Genetic Tests in the United States: Work of the Task Force on Genetic Testing

Data withholding in academic genetics: evidence from a national survey

Withdrawing FDA approval of midodrine after marketing

The evidence dilemma and cultural change

How does the mode of inheritance of a genetic condition influence families? A study of guilt, blame, stigma, and understanding of inheritance and reproductive risks in families with X-linked and autosomal recessive diseases

Expanding newborn screening: how good is the evidence?

The media and public reaction to genetic research

What Role for Public Health in Genetics and Vice Versa?

Management of hyperbilirubinemia: quality of evidence and cost

Are Genetic Tests Adequately Regulated?

The new genetics: Genetic testing and public policy

Does knowledge about the genetics of breast cancer differ between nongeneticist physicians who do or do not discuss or order BRCA testing?

Scientists' and science writers' experiences reporting genetic discoveries: Toward an ethic of trust in science journalism

Mapping the human genome: An assessment of media coverage and public reaction

The Quality of Media Reports on Discoveries Related to Human Genetic Diseases

Adoption of Liquid-Based Cervical Cancer Screening Tests by Family Physicians and Gynecologists

PUTTING THE SEARCH FOR GENES IN PERSPECTIVE

Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease

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