Genetic Risks to the Mother and the Infant: Assessment, Counseling, and Management

Por Shapira, Stuart K., Dolan, Siobhan
Publicado em 2006

Invited Commentary: Male Reproductive System Congenital Malformations and the Risk of Autism Spectrum Disorder

Por Schieve, Laura A., Shapira, Stuart K.
Publicado no Am J Epidemiol (2018)

Expanding Diagnostic Testing beyond Cytogenetics: Implications for Birth Defects Research and Surveillance

Por Jackson, Jodi M., Druschel, Charlotte M., Shapira, Stuart K.
Publicado no Birth Defects Res A Clin Mol Teratol (2013)

Maternal Vasoactive Exposures, Amniotic Bands, and Terminal Transverse Limb Defects

Por Werler, Martha M., Bosco, Jaclyn L. F., Shapira, Stuart K.
Publicado em 2009

Survival Disparities Associated with Congenital Diaphragmatic Hernia

Por Hinton, Cynthia F., Siffel, Csaba, Correa, Adolfo, Shapira, Stuart K.
Publicado no Birth Defects Res (2017)

Identification of Primary Congenital Hypothyroidism Based on Two Newborn Screens — Utah, 2010–2016

Por Jones, David E., Hart, Kim, Shapira, Stuart K., Murray, Mary, Atkinson-Dunn, Robyn, Rohrwasser, Andreas
Publicado no MMWR Morb Mortal Wkly Rep (2018)

Single newborn screen or routine second screening for primary congenital hypothyroidism

Por Shapira, Stuart K., Hinton, Cynthia F., Held, Patrice K., Jones, Elizabeth, Hannon, W. Harry, Ojodu, Jelili
Publicado no Mol Genet Metab (2015)

Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states

Por Held, Patrice K., Shapira, Stuart K., Hinton, Cynthia F., Jones, Elizabeth, Hannon, W. Harry, Ojodu, Jelili
Publicado no Mol Genet Metab (2015)

Association of Paternal Age and Risk for Major Congenital Anomalies from the National Birth Defects Prevention Study, 1997–2004

Por Green, Ridgely Fisk, Devine, Owen, Crider, Krista S., Olney, Richard S., Archer, Natalie, Olshan, Andrew F., Shapira, Stuart K.
Publicado em 2010

Associations Between the 2nd to 4th Digit Ratio and Autism Spectrum Disorder in Population-Based Samples of Boys and Girls: Findings from the Study to Explore Early Development

Por Schieve, Laura A., Tian, Lin, Dowling, Nicole, Croen, Lisa, Hoover-Fong, Julie, Alexander, Aimee, Shapira, Stuart K.
Publicado no J Autism Dev Disord (2018)

Treatment Discontinuation by 3 Years After Levothyroxine Initiation among Children Diagnosed with Congenital Hypothyroidism

Por Kemper, Alex R., Grosse, Scott D., Baker, Mei, Pollock, Allison J., Hinton, Cynthia F., Shapira, Stuart K.
Publicado no J Pediatr (2020)

What we Don’t Know Can Hurt us: Nonresponse Bias Assessment in Birth Defects Research

Por Strassle, Paula D., Cassell, Cynthia H., Shapira, Stuart K., Tinker, Sarah C., Meyer, Robert E., Grosse, Scott D.
Publicado no Birth Defects Res A Clin Mol Teratol (2015)

Treated Prevalence of Attention-Deficit/Hyperactivity Disorder Increased from 2009 to 2015 Among School-Aged Children and Adolescents in the United States

Por Nyarko, Kwame A., Grosse, Scott D., Danielson, Melissa L., Holbrook, Joseph R., Visser, Susanna N., Shapira, Stuart K.
Publicado no J Child Adolesc Psychopharmacol (2017)

Paternal occupation and birth defects: findings from the National Birth Defects Prevention Study

Por Desrosiers, Tania A., Herring, Amy H., Shapira, Stuart K., Hooiveld, Mariette, Luben, Tom J., Herdt-Losavio, Michele L., Lin, Shao, Olshan, Andrew F.
Publicado em 2012

CDC Grand Rounds: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease

Por Grosse, Scott D., Riehle-Colarusso, Tiffany, Gaffney, Marcus, Mason, Craig A., Shapira, Stuart K., Sontag, Marci K., Braun, Kim Van Naarden, Iskander, John
Publicado no MMWR Morb Mortal Wkly Rep (2017)

Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome

Por Heilstedt, Heidi A., Ballif, Blake C., Howard, Leslie A., Lewis, Richard A., Stal, Samuel, Kashork, Catherine D., Bacino, Carlos A., Shapira, Stuart K., Shaffer, Lisa G.
Publicado em 2003

Detecting moderate or complex congenital heart defects in adults from an electronic health records system

Por Diallo, Alpha Oumar, Krishnaswamy, Asha, Shapira, Stuart K, Oster, Matthew E, George, Mary G, Adams, Jenna C, Walker, Elizabeth R, Weiss, Paul, Ali, Mohammed K, Book, Wendy
Publicado no J Am Med Inform Assoc (2018)

ADHD Medication Use During Pregnancy and Risk for Selected Birth Defects: National Birth Defects Prevention Study, 1998–2011

Por Anderson, Kayla N., Dutton, Annelise C., Broussard, Cheryl S., Farr, Sherry L., Lind, Jennifer N., Visser, Susanna N., Ailes, Elizabeth C., Shapira, Stuart K., Reefhuis, Jennita, Tinker, Sarah C.
Publicado no J Atten Disord (2018)

A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma (NEMO)

Por Zonana, Jonathan, Elder, Melissa E., Schneider, Lynda C., Orlow, Seth J., Moss, Celia, Golabi, Mahin, Shapira, Stuart K., Farndon, Peter A., Wara, Diane W., Emmal, Stephanie A., Ferguson, Betsy M.
Publicado em 2000

Infants with Congenital Disorders Identified Through Newborn Screening — United States, 2015–2017

Por Sontag, Marci K., Yusuf, Careema, Grosse, Scott D., Edelman, Sari, Miller, Joshua I., McKasson, Sarah, Kellar-Guenther, Yvonne, Gaffney, Marcus, Hinton, Cynthia F., Cuthbert, Carla, Singh, Sikha, Ojodu, Jelili, Shapira, Stuart K.
Publicado no MMWR Morb Mortal Wkly Rep (2020)