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Increase in congenital hypothyroidism in New York State and in the United States

Molecular genetics and metabolism, 2007-07, Vol.91 (3), p.268-277

2007

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Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas

Pediatrics (Evanston), 2010-05, Vol.125 Suppl 2, p.S37

2010

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Use of Newborn Screening Program Blood Spots for Exposure Assessment: Declining Levels of Perfluorinated Compounds in New York State Infants

Environmental science & technology, 2008-07, Vol.42 (14), p.5361-5367

2008

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High-Throughput Multiplexed T-Cell-Receptor Excision Circle Quantitative PCR Assay with Internal Controls for Detection of Severe Combined Immunodeficiency in Population-Based Newborn Screening

Clinical chemistry (Baltimore, Md.), 2010-09, Vol.56 (9), p.1466-1474

2010

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Newborn screening for autism: in search of candidate biomarkers

Biomarkers in medicine, 2013-04, Vol.7 (2), p.247-260

2013

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A Multiplex Immunoassay Using the Guthrie Specimen to Detect T-Cell Deficiencies Including Severe Combined Immunodeficiency Disease

Clinical chemistry (Baltimore, Md.), 2010-09, Vol.56 (9), p.1460-1465

2010

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Newborn Screening for Cystic Fibrosis by Use of a Multiplex Immunoassay

Clinical chemistry (Baltimore, Md.), 2010-03, Vol.56 (3), p.445-450

2010

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Update: Newborn Screening for Endocrinopathies

Endocrinology and metabolism clinics of North America, 2009-12, Vol.38 (4), p.827-837

2009

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Neonatal screening by DNA microarray: spots and chips

Nature reviews. Genetics, 2005-02, Vol.6 (2), p.147-151

2005

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Enhancing newborn screening for tyrosinemia type I

Clinical chemistry (Baltimore, Md.), 2008-04, Vol.54 (4), p.627-629

2008

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A qualitative analysis of emerging adult black men's sexual decision-making behavior and substance use

Journal of ethnicity in substance abuse, 2016-10, Vol.15 (4), p.386-404

2016

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Newborn screening for metabolic disorders: how are we doing, and where are we going?

Clinical chemistry (Baltimore, Md.), 2012-02, Vol.58 (2), p.324-331

2012

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HIV Apartheid: Black Politics and the Fight Against Health Inequities

Pass, Kenneth

2024

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Improved immunoassay for the detection of severe combined immunodeficiency

Clinical chemistry (Baltimore, Md.), 2011-08, Vol.57 (8), p.1207-1209

2011

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Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: Under-representation of the common c.985 A > G mutation in the New York state population

American journal of medical genetics. Part A, 2008-03, Vol.146A (5), p.610-619

2008

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US Newborn Screening System Guidelines II: Follow-up of Children, Diagnosis, Management, and Evaluation Statement of the Council of Regional Networks for Genetic Services (CORN)

The Journal of pediatrics, 2000-10, Vol.137 (4), p.S1-S47

2000

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A microsphere-based assay for mutation analysis of the biotinidase gene using dried blood spots

Journal of pediatric genetics (Birmingham, Ala.), 2012-09, Vol.1 (3), p.153-160

2012

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How reliable is newborn screening for congenital adrenal hyperplasia?

Nature clinical practice. Endocrinology & metabolism, 2006-02, Vol.2 (2), p.74-75

Pass, Kenneth A

2006

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Emergency preparedness for newborn screening and genetic services

Genetics in medicine, 2009-06, Vol.11 (6), p.455-464

2009

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Not as pink as you think

Pediatrics (Evanston), 2003-03, Vol.111 (3), p.670

Pass, Kenneth A

2003

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Simultaneous measurement of antibodies to three HIV-1 antigens in newborn dried blood-spot specimens using a multiplexed microsphere-based immunoassay

Early human development, 2001-08, Vol.64 (1), p.21-25

2001

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Commentary on: Use of Microsphere Immunoassay for Simplified Multianalyte Screening of Thyrotropin and Thyroxine in Dried Blood Spots from Newborns

Clinical chemistry (Baltimore, Md.), 2003-02, Vol.49 (2), p.336-336

Pass, Kenneth A

2003

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Perinatal transfer of genetic information: developing an algorithm for reporting cystic fibrosis prenatal test results to the newborn screening program

Genetics in medicine, 2008-11, Vol.10 (11), p.805-810

2008

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Evaluation of glucose-6-phosphate dehydrogenase stability in blood samples under different collection and storage conditions

Clinical chemistry (Baltimore, Md.), 2005-06, Vol.51 (6), p.1080-1081

2005

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Lysosomal storage diseases: Diagnostic confirmation and management of presymptomatic individuals

Genetics in medicine, 2011-05, Vol.13 (5), p.457-484

2011

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Increase in congenital hypothyroidism in New York State and in the United States

Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas

Use of Newborn Screening Program Blood Spots for Exposure Assessment: Declining Levels of Perfluorinated Compounds in New York State Infants

High-Throughput Multiplexed T-Cell-Receptor Excision Circle Quantitative PCR Assay with Internal Controls for Detection of Severe Combined Immunodeficiency in Population-Based Newborn Screening

Newborn screening for autism: in search of candidate biomarkers

A Multiplex Immunoassay Using the Guthrie Specimen to Detect T-Cell Deficiencies Including Severe Combined Immunodeficiency Disease

Newborn Screening for Cystic Fibrosis by Use of a Multiplex Immunoassay

Update: Newborn Screening for Endocrinopathies

Neonatal screening by DNA microarray: spots and chips

Enhancing newborn screening for tyrosinemia type I

A qualitative analysis of emerging adult black men's sexual decision-making behavior and substance use

Newborn screening for metabolic disorders: how are we doing, and where are we going?

HIV Apartheid: Black Politics and the Fight Against Health Inequities

Improved immunoassay for the detection of severe combined immunodeficiency

Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: Under-representation of the common c.985 A > G mutation in the New York state population

US Newborn Screening System Guidelines II: Follow-up of Children, Diagnosis, Management, and Evaluation Statement of the Council of Regional Networks for Genetic Services (CORN)

A microsphere-based assay for mutation analysis of the biotinidase gene using dried blood spots

How reliable is newborn screening for congenital adrenal hyperplasia?

Emergency preparedness for newborn screening and genetic services

Not as pink as you think

Simultaneous measurement of antibodies to three HIV-1 antigens in newborn dried blood-spot specimens using a multiplexed microsphere-based immunoassay

Commentary on: Use of Microsphere Immunoassay for Simplified Multianalyte Screening of Thyrotropin and Thyroxine in Dried Blood Spots from Newborns

Perinatal transfer of genetic information: developing an algorithm for reporting cystic fibrosis prenatal test results to the newborn screening program

Evaluation of glucose-6-phosphate dehydrogenase stability in blood samples under different collection and storage conditions

Lysosomal storage diseases: Diagnostic confirmation and management of presymptomatic individuals

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