Publications by authors named "Kenneth Pass"

Claim this Profile
B
Beyond criminalization: reconsidering HIV criminalization in an era of reform.
Trevor Hoppe, Alexander McClelland, Kenneth Pass

Curr Opin HIV AIDS· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A qualitative analysis of emerging adult black men's sexual decision-making behavior and substance use.
Kenneth M Pass, Sinead N Younge, Angelica Geter, Maliyhah Al-Bayan, Bruce H Wade

J Ethn Subst Abuse· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
Chrysovalanto Mamasoula, R Reid Prentice, Tomasz Pierscionek, Faith Pangilinan, James L Mills, Kenneth Pass

Circ Cardiovasc Genet· August 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Newborn screening for autism: in search of candidate biomarkers.
Gerald J Mizejewski, Barbara Lindau-Shepard, Kenneth A Pass

Biomark Med· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A microsphere-based assay for mutation analysis of the biotinidase gene using dried blood spots.
Barbara Lindau-Shepard, David K Janik, Kenneth A Pass

J Pediatr Genet· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Newborn screening for metabolic disorders: how are we doing, and where are we going?
Michael J Bennett, Piero Rinaldo, Bridget Wilcken, Kenneth A Pass, Michael S Watson

Clin Chem· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Improved immunoassay for the detection of severe combined immunodeficiency.
David K Janik, Barbara Lindau-Shepard, Bent Nørgaard-Pedersen, Carsten Heilmann, Kenneth A Pass

Clin Chem· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative.
Richard J Auchus, Selma Feldman Witchel, Kelly R Leight, Javier Aisenberg, Ricardo Azziz, Kenneth A Pass

Int J Pediatr Endocrinol· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.
David M S McHugh, Cynthia A Cameron, Jose E Abdenur, Mahera Abdulrahman, Ona Adair, Kenneth A Pass

Genet Med· March 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
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.
Jacalyn L Gerstel-Thompson, Jonathan F Wilkey, Jennifer C Baptiste, Jennifer S Navas, Sung-Yun Pai, Kenneth A Pass

Clin Chem· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A multiplex immunoassay using the Guthrie specimen to detect T-cell deficiencies including severe combined immunodeficiency disease.
David K Janik, Barbara Lindau-Shepard, Anne Marie Comeau, Kenneth A Pass

Clin Chem· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas.
Cynthia F Hinton, Katharine B Harris, Lynette Borgfeld, Margaret Drummond-Borg, Roger Eaton, Kenneth A Pass

Pediatrics· May 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Newborn screening for cystic fibrosis by use of a multiplex immunoassay.
Barbara A Lindau-Shepard, Kenneth A Pass

Clin Chem· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Update: newborn screening for endocrinopathies.
Kenneth A Pass, Eurico Carmago Neto

Endocrinol Metab Clin North Am· December 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Emergency preparedness for newborn screening and genetic services.
Kenneth A Pass, Jess Thoene, Michael S Watson

Genet Med· June 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory report.
Ira M Lubin, Margaret M McGovern, Zoe Gibson, Susan J Gross, Elaine Lyon, Kenneth Pass

J Mol Diagn· March 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Perinatal transfer of genetic information: developing an algorithm for reporting cystic fibrosis prenatal test results to the newborn screening program.
Ellen S Regalado, Elinor Langfelder-Schwind, Andrew D Corwin, Kenneth A Pass

Genet Med· November 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Use of newborn screening program blood spots for exposure assessment: declining levels of perluorinated compounds in New York State infants.
Henry M Spliethoff, Lin Tao, Shannon M Shaver, Kenneth M Aldous, Kenneth A Pass

Environ Sci Technol· July 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Enhancing newborn screening for tyrosinemia type I.
Kenneth A Pass, Mark Morrissey

Clin Chem· April 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
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.
Matthew J Nichols, Carlos A Saavedra-Matiz, Kenneth A Pass, Michele Caggana

Am J Med Genet A· March 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Increase in congenital hypothyroidism in New York State and in the United States.
Katharine B Harris, Kenneth A Pass

Mol Genet Metab· July 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pilot programs in newborn screening.
Kenneth Pass, Nancy S Green, Fred Lorey, John Sherwin, Anne Marie Comeau

Ment Retard Dev Disabil Res Rev· March 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
How reliable is newborn screening for congenital adrenal hyperplasia?
Kenneth A Pass

Nat Clin Pract Endocrinol Metab· February 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Folate-related genes and omphalocele.
James L Mills, Charlotte M Druschel, Faith Pangilinan, Kenneth Pass, Christopher Cox

Am J Med Genet A· July 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evaluation of glucose-6-phosphate dehydrogenase stability in blood samples under different collection and storage conditions.
Simone M Castro, Raquel Weber, Vivian Dadalt, Vanessa F Santos, George J Reclos, Kenneth A Pass

Clin Chem· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis