Genetics and Public Health in the 20th Century

por Caggana, Michele
Publicado 2001

The Impact of Post-Analytical Tools on New York Screening for Krabbe Disease and Pompe Disease

por Martin, Monica M., Wilson, Ryan, Caggana, Michele, Orsini, Joseph J.
Publicado en Int J Neonatal Screen (2020)

Newborn Screening for Krabbe’s Disease

por Orsini, Joseph J., Saavedra-Matiz, Carlos A., Gelb, Michael H., Caggana, Michele
Publicado en J Neurosci Res (2016)

Newborn Screening: From Guthrie to Whole Genome Sequencing

por Caggana, Michele, Jones, Elizabeth A., Shahied, S.I., Tanksley, Susan, Hermerath, Cheryl A., Lubin, Ira M.
Publicado 2013

The Impact of Seasonal Changes on Thyroxine and Thyroid-Stimulating Hormone in Newborns

por McMahon, Rebecca, DeMartino, Lenore, Sowizral, Mycroft, Powers, Diana, Tracy, Melissa, Caggana, Michele, Tavakoli, Norma P.
Publicado en Int J Neonatal Screen (2021)

Lysosomal storage disorder 4+1 multiplex assay for newborn screening using tandem mass spectrometry: Application to a small-scale population study for five lysosomal storage disord...

por Orsini, Joseph J., Martin, Monica M., Showers, Amanda L., Bodamer, Olaf A., Zhang, X. Kate, Gelb, Michael H., Caggana, Michele
Publicado 2012

Abnormal Newborn Screening Data and Acylcarnitines in HIV/ARV-Exposed Infants

por Kirmse, Brian, Hobbs, Charlotte V., Peter, Inga, LaPlante, Bryan, Caggana, Michele, Kloke, Karen, Raymond, Kimiyo, Summar, Marshall, Borkowsky, William
Publicado en Pediatr Infect Dis J (2013)

Eliciting parental support for the use of newborn blood spots for pediatric research

por Yeung, Edwina H., Louis, Germaine Buck, Lawrence, David, Kannan, Kurunthachalam, McLain, Alexander C., Caggana, Michele, Druschel, Charlotte, Bell, Erin
Publicado en BMC Med Res Methodol (2016)

Temporal Trends of Polybrominated Diphenyl Ethers (PBDEs) in the Blood of Newborns from New York State during 1997 through 2011: Analysis of Dried Blood Spots from the Newborn Scre...

por Ma, Wan-Li, Yun, Sehun, Bell, Erin M., Druschel, Charlotte M., Caggana, Michele, Aldous, Kenneth M., Buck Louis, Germaine M., Kannan, Kurunthachalam
Publicado 2013

Genetic and epigenetic regulation of AHR gene expression in MCF-7 breast cancer cells: role of the proximal promoter GC-rich region

por Englert, Neal A., Turesky, Robert J., Han, Weiguo, Bessette, Erin E., Spivack, Simon D., Caggana, Michele, Spink, David C., Spink, Barbara C.
Publicado 2012

Analysis of polychlorinated biphenyls and organochlorine pesticides in archived dried blood spots and its application to track temporal trends of environmental chemicals in newborn...

por Ma, Wan-Li, Gao, Chongjing, Bell, Erin M., Druschel, Charlotte M., Caggana, Michele, Aldous, Kenneth M., Buck Louis, Germaine M., Kannan, Kurunthachalam
Publicado 2014

Newborn Screening for X-Linked Adrenoleukodystrophy

por Moser, Ann B., Jones, Richard O., Hubbard, Walter C., Tortorelli, Silvia, Orsini, Joseph J., Caggana, Michele, Vogel, Beth H., Raymond, Gerald V.
Publicado en Int J Neonatal Screen (2016)

Folate and Vitamin B12 Related Genes and Risk for Omphalocele

por Mills, James L., Carter, Tonia C., Kay, Denise M., Browne, Marilyn, Brody, Lawrence C., Liu, Aiyi, Romitti, Paul A., Caggana, Michele, Druschel, Charlotte
Publicado 2011

Mortality of New York children with sickle cell disease identified through newborn screening

por Wang, Ying, Liu, Gang, Caggana, Michele, Kennedy, Joseph, Zimmerman, Regina, Oyeku, Suzette O., Werner, Ellen M., Grant, Althea M., Green, Nancy S., Grosse, Scott D.
Publicado en Genet Med (2014)

Ordering Molecular Genetic Tests and Reporting Results: Practices in Laboratory and Clinical Settings

por Lubin, Ira M., Caggana, Michele, Constantin, Carolyn, Gross, Susan J., Lyon, Elaine, Pagon, Roberta A., Trotter, Tracy L., Wilson, Jean Amos, McGovern, Margaret M.
Publicado 2008

Sickle cell disease incidence among newborns in New York State by maternal race/ethnicity and nativity

por Wang, Ying, Kennedy, Joseph, Caggana, Michele, Zimmerman, Regina, Thomas, Sanil, Berninger, John, Harris, Katharine, Green, Nancy S., Oyeku, Suzette, Hulihan, Mary, Grant, Althea M., Grosse, Scott D
Publicado en Genet Med (2012)

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

por Reeves, Sarah L., Madden, Brian, Wu, Meng, Miller, Lauren S., Anders, David, Caggana, Michele, Cogan, Lindsay W., Kleyn, Mary, Hurden, Isabel, Freed, Gary L., Dombkowski, Kevin J.
Publicado en Health Serv Res (2020)

Evaluation of Genes Involved in Limb Development, Angiogenesis, and Coagulation as Risk Factors for Congenital Limb Deficiencies

por Browne, Marilyn L., Carter, Tonia C., Kay, Denise M., Kuehn, Devon, Brody, Lawrence C., Romitti, Paul A., Liu, Aiyi, Caggana, Michele, Druschel, Charlotte M., Mills, James L.
Publicado 2012

Fragile X protein in newborn dried blood spots

por Adayev, Tatyana, LaFauci, Giuseppe, Dobkin, Carl, Caggana, Michele, Wiley, Veronica, Field, Michael, Wotton, Tiffany, Kascsak, Richard, Nolin, Sarah L, Glicksman, Anne, Hosmer, Nicole, Brown, W Ted
Publicado en BMC Med Genet (2014)

Newborn screening for congenital adrenal hyperplasia in New York State

por Pearce, Melissa, DeMartino, Lenore, McMahon, Rebecca, Hamel, Rhonda, Maloney, Breanne, Stansfield, Daniele-Marisa, McGrath, Emily C., Occhionero, Amanda, Gearhart, Adam, Caggana, Michele, Tavakoli, Norma P.
Publicado en Mol Genet Metab Rep (2016)