M. Kleyn

发表

Michigan BioTrust for Health: Public Support for Using Residual Dried Blood Spot Samples for Health Research

D. Duquette, C. Langbo, J. Bach, 2012, Public Health Genomics.

The financial and time burden associated with phenylketonuria treatment in the United States

L. Prosser, S. Grosse, Norma-Jean E. Simon, 2019, Molecular genetics and metabolism reports.

Current Practices for U.S. Newborn Screening of Pompe Disease and MPSI

Ayesha Ahmad, Rachel Fisher, Elizabeth G. Ames, 2020, International journal of neonatal screening.

Evaluation of genetic counseling among cystic fibrosis carriers, Michigan Newborn Screening

D. Homnick, J. Schuen, E. Carmany, 2013, Pediatric pulmonology.

Incidence, demographic characteristics, and geographic distribution of sickle cell trait and sickle cell anemia births in Michigan, 1997–2014

K. Spector-Bagdady, S. Reeves, H. Jary, 2019, Molecular genetics & genomic medicine.

Performance Metrics After Changes in Screening Protocol for Congenital Hypothyroidism

G. Birbeck, R. Romero, N. Paneth, 2012, Pediatrics.

Pneumococcal vaccination coverage among children with sickle cell anemia, sickle cell trait, and normal hemoglobin

H. Jary, Jennifer P Gondhi, K. Dombkowski, 2018, Pediatric blood & cancer.

Performance of ICD-10-CM diagnosis codes for identifying children with Sickle Cell Anemia.

G. Freed, M. Caggana, K. Dombkowski, 2020, Health services research.

Evaluation of Pulse Oximetry Screening Rates Among the Midwife-Attended Out-of-Hospital Birth Community in Michigan.

C. Fussman, M. Kleyn, E. Withrow, 2019, Journal of midwifery & women's health.

Identifying sickle cell disease cases using administrative claims.

Erika Garcia, K. Dombkowski, Michelle Housey, 2014, Academic pediatrics.

Predictors of insufficient sweat production during confirmatory testing for cystic fibrosis

D. Homnick, S. Korzeniewski, J. Schuen, 2011, Pediatric pulmonology.

Newborn screening follow-up within the lifespan context: Michigan's experience.

S. Korzeniewski, V. Grigorescu, W. Whitten-Shurney, 2010, American journal of preventive medicine.

Health outcomes and services in children with sickle cell trait, sickle cell anemia, and normal hemoglobin.

H. Jary, Jennifer P Gondhi, K. Dombkowski, 2019, Blood advances.

Screening for congenital hypothyroidism in newborns transferred to neonatal intensive care

R. Romero, T. Chaiworapongsa, S. Korzeniewski, 2012, Archives of Disease in Childhood: Fetal and Neonatal Edition.

Congenital Hypothyroidism Long-Term Follow-up Project: Navigating the Rough Waters of a Multi-Center, Multi-State Public Health Project

E. Eugster, Lisa A. Gorman, K. Wintergerst, 2014, Journal of Genetic Counseling.

Transient hypothyroidism at 3-year follow-up among cases of congenital hypothyroidism detected by newborn screening.

G. Birbeck, R. Romero, N. Paneth, 2013, The Journal of pediatrics.

Newborn Screening Collection and Delivery Processes in Michigan Birthing Hospitals: Strategies to Improve Timeliness

Amy L. Cochran, A. Cochran, B. Tarini, 2018, Maternal and Child Health Journal.

QA / QC 2 – Strategies to Reduce False Positives and False Negatives ( Part 2 ) Tuesday , Oct . 28 – 10 : 30 am-12 : 00 pm Moderators –

B. Taffe, M. Seeterlin, M. Kleyn, 2022 .

Variation in immunoreactive trypsinogen concentrations among michigan newborns and implications for cystic fibrosis newborn screening

S. Grosse, S. Korzeniewski, S. Nasr, 2011, Pediatric pulmonology.

Maternal weathering and risk of preterm delivery.

J. Kaufman, P. O’Campo, J. Culhane, 2009, American journal of public health.

From Newborn Screening to Population Health Research: Implementation of the Michigan BioTrust for Health

F. Downes, C. Langbo, J. Bach, 2013, Public health reports.

Congenital Hypothyroidism 3-Year Follow-Up Project: Region 4 Midwest Genetics Collaborative Results

Julie A. Moore, R. Menon, E. Eugster, 2018, International journal of neonatal screening.

Predictors of insufficient sweat production during confirmatory testing for cystic fibrosis

D. Homnick, S. Korzeniewski, J. Schuen, 2011, Pediatric pulmonology.

Newborn Tandem Mass Spectroscopy Screening for Adenosine Deaminase Deficiency-First Two Years' Experience.

E. Secord, N. Hartog, K. Walkovich, 2022, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Missed Cystic Fibrosis Newborn Screening Cases due to Immunoreactive Trypsinogen Levels below Program Cutoffs: A National Survey of Risk Factors

M. Caggana, A. Comeau, B. Therrell, 2022, International Journal of Neonatal Screening.

Use of Online Newborn Screening Educational Resources for the Education of Expectant Parents: An Improvement in Equity

M. Kleyn, Kristen Thompson, Shelby Atkinson, 2022, International Journal of Neonatal Screening.

Five cases of missed cystic fibrosis heterozygous mutations identified after a positive newborn screen on a sibling

J. Schuen, I. Abdulhamid, S. Nasr, 2022, Respiratory medicine case reports.