Publications by authors named "Kenneth A Pass"

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Newborn screening for autism: in search of candidate biomarkers.
Gerald J Mizejewski, Barbara Lindau-Shepard, Kenneth A Pass

Biomark Med· April 2013

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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

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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

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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

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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

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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

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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.
Jacalyn L Gerstel-Thompson, Jonathan F Wilkey, Jennifer C Baptiste, Jennifer S Navas, Sung-Yun Pai, Kenneth A Pass

Clin Chem· September 2010

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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

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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.
Cynthia F Hinton, Katharine B Harris, Lynette Borgfeld, Margaret Drummond-Borg, Roger Eaton, Kenneth A Pass

Pediatrics· May 2010

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Newborn screening for cystic fibrosis by use of a multiplex immunoassay.
Barbara A Lindau-Shepard, Kenneth A Pass

Clin Chem· March 2010

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Update: newborn screening for endocrinopathies.
Kenneth A Pass, Eurico Carmago Neto

Endocrinol Metab Clin North Am· December 2009

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Emergency preparedness for newborn screening and genetic services.
Kenneth A Pass, Jess Thoene, Michael S Watson

Genet Med· June 2009

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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

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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

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Enhancing newborn screening for tyrosinemia type I.
Kenneth A Pass, Mark Morrissey

Clin Chem· April 2008

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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.
Matthew J Nichols, Carlos A Saavedra-Matiz, Kenneth A Pass, Michele Caggana

Am J Med Genet A· March 2008

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Increase in congenital hypothyroidism in New York State and in the United States.
Katharine B Harris, Kenneth A Pass

Mol Genet Metab· July 2007

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How reliable is newborn screening for congenital adrenal hyperplasia?
Kenneth A Pass

Nat Clin Pract Endocrinol Metab· February 2006

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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

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Neonatal screening by DNA microarray: spots and chips.
Nancy S Green, Kenneth A Pass

Nat Rev Genet· February 2005

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Characterization of beta-globin haplotypes using blood spots from a population-based cohort of newborns with homozygous HbS.
Dana C Crawford, Michele Caggana, Katharine B Harris, Fred Lorey, Claudia Nash, Kenneth A Pass

Genet Med· March 2003

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Not as pink as you think!
Kenneth A Pass

Pediatrics· March 2003

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Report from a workshop on multianalyte microsphere assays.
Marie C Earley, Robert F Vogt, Howard M Shapiro, Francis F Mandy, Kathryn L Kellar, Kenneth A Pass

Cytometry· October 2002

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