Profil bibliographique

Michele A. Lloyd-Puryear

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

97Publications signalées

5012Citations signalées

1Affiliations récentes

Institutions déclarées

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Domaines associés

Metabolism and Genetic DisordersGenomics and Rare DiseasesBRCA gene mutations in cancerPrenatal Screening and DiagnosticsChild and Adolescent Health

Publications récentes

Accès ouvert 2025 articleOpenAlex

The importance of residual newborn screening dried blood spots, 2025 revision: A position statement of the American College of Medical Genetics and Genomics (ACMG)

Nancy C. Rose, Michele Caggana, Mary Beth Dinulos, Leslie P. Francis et autres

3 citationsGenetics in Medicine

Accès ouvert 2024 articleOpenAlex

Newborn Screening for Six Primary Conditions in a Clinical Setting in Morocco

Sara El Janahi, Mounir Filali, Zakia Boudar, Amina Akhattab et autres

4 citationsInternational Journal of Neonatal Screening

Accès ouvert 2023 articleOpenAlex

Factors influencing creatine kinase-MM concentrations in newborns and implications for newborn screening for Duchenne muscular dystrophy

Breanne Maloney, Sunju Park, Mycroft Sowizral, Isa Brackett et autres

9 citationsClinical Biochemistry

Accès ouvert 2023 articleOpenAlex

Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission

Frédéric B. Piel, David C. Rees, Michael R. DeBaun, Obiageli Nnodu et autres

172 citationsThe Lancet Haematology

Accès ouvert 2023 articleOpenAlex

Newborn screening for Duchenne muscular dystrophy: A two‐year pilot study

Norma P. Tavakoli, Dorota Gruber, Niki Armstrong, Wendy K. Chung et autres

33 citationsAnnals of Clinical and Translational Neurology

Accès ouvert 2022 articleOpenAlex

Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot

M. J. Hartnett, Michele A. Lloyd-Puryear, Norma P. Tavakoli, Julia Wynn et autres

23 citationsInternational Journal of Neonatal Screening

2022 articleOpenAlex

Considerations for policymakers for improving health care through telegenetics: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)

Heather Williams, Lila Aiyar, Mary Beth Dinulos, David B. Flannery et autres

3 citationsGenetics in Medicine

Accès ouvert 2022 articleOpenAlex

The Progress and Future of US Newborn Screening

Michael S. Watson, Michele A. Lloyd-Puryear, R. Rodney Howell

53 citationsInternational Journal of Neonatal Screening

Accès ouvert 2022 articleOpenAlex

Metagenomics Approaches to Investigate the Neonatal Gut Microbiome

Zakia Boudar, Sofia Sehli, Sara El Janahi, Najib Al Idrissi et autres

11 citationsFrontiers in Pediatrics

Accès ouvert 2022 articleOpenAlex

Newborn screening for neurodevelopmental diseases: Are we there yet?

Wendy K. Chung, Jonathan S. Berg, Jeffrey R. Botkin, Steven E. Brenner et autres

28 citationsAmerican Journal of Medical Genetics Part C Seminars in Medical Genetics

Accès ouvert 2022 articleOpenAlex

Newborn screening for Duchenne muscular dystrophy‐early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy

Dorota Gruber, Michele A. Lloyd-Puryear, Niki Armstrong, Mena Scavina et autres

25 citationsAmerican Journal of Medical Genetics Part C Seminars in Medical Genetics

Accès ouvert 2020 articleOpenAlex

Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism

Peter W. Stacpoole, Andrew E. Mulberg, Jerry Vockley, Lynne Yao et autres

0 citationsCarolina Digital Repository (University of North Carolina at Chapel Hill)

Profil ORCID Notice OpenAlex

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