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

Bằng Shapira, Stuart K., Dolan, Siobhan
Được phát hành 2006

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

Bằng Schieve, Laura A., Shapira, Stuart K.
Xuất bản năm Am J Epidemiol (2018)

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

Bằng Jackson, Jodi M., Druschel, Charlotte M., Shapira, Stuart K.
Xuất bản năm Birth Defects Res A Clin Mol Teratol (2013)

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

Bằng Werler, Martha M., Bosco, Jaclyn L. F., Shapira, Stuart K.
Được phát hành 2009

Survival Disparities Associated with Congenital Diaphragmatic Hernia

Bằng Hinton, Cynthia F., Siffel, Csaba, Correa, Adolfo, Shapira, Stuart K.
Xuất bản năm Birth Defects Res (2017)

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

Bằng Jones, David E., Hart, Kim, Shapira, Stuart K., Murray, Mary, Atkinson-Dunn, Robyn, Rohrwasser, Andreas
Xuất bản năm MMWR Morb Mortal Wkly Rep (2018)

Single newborn screen or routine second screening for primary congenital hypothyroidism

Bằng Shapira, Stuart K., Hinton, Cynthia F., Held, Patrice K., Jones, Elizabeth, Hannon, W. Harry, Ojodu, Jelili
Xuất bản năm Mol Genet Metab (2015)

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

Bằng Held, Patrice K., Shapira, Stuart K., Hinton, Cynthia F., Jones, Elizabeth, Hannon, W. Harry, Ojodu, Jelili
Xuất bản năm Mol Genet Metab (2015)

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

Bằng Green, Ridgely Fisk, Devine, Owen, Crider, Krista S., Olney, Richard S., Archer, Natalie, Olshan, Andrew F., Shapira, Stuart K.
Được phát hành 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

Bằng Schieve, Laura A., Tian, Lin, Dowling, Nicole, Croen, Lisa, Hoover-Fong, Julie, Alexander, Aimee, Shapira, Stuart K.
Xuất bản năm J Autism Dev Disord (2018)

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

Bằng Kemper, Alex R., Grosse, Scott D., Baker, Mei, Pollock, Allison J., Hinton, Cynthia F., Shapira, Stuart K.
Xuất bản năm J Pediatr (2020)

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

Bằng Strassle, Paula D., Cassell, Cynthia H., Shapira, Stuart K., Tinker, Sarah C., Meyer, Robert E., Grosse, Scott D.
Xuất bản năm 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

Bằng Nyarko, Kwame A., Grosse, Scott D., Danielson, Melissa L., Holbrook, Joseph R., Visser, Susanna N., Shapira, Stuart K.
Xuất bản năm J Child Adolesc Psychopharmacol (2017)

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

Bằng Desrosiers, Tania A., Herring, Amy H., Shapira, Stuart K., Hooiveld, Mariette, Luben, Tom J., Herdt-Losavio, Michele L., Lin, Shao, Olshan, Andrew F.
Được phát hành 2012

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

Bằng Grosse, Scott D., Riehle-Colarusso, Tiffany, Gaffney, Marcus, Mason, Craig A., Shapira, Stuart K., Sontag, Marci K., Braun, Kim Van Naarden, Iskander, John
Xuất bản năm MMWR Morb Mortal Wkly Rep (2017)

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

Bằng 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.
Được phát hành 2003

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

Bằng 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
Xuất bản năm J Am Med Inform Assoc (2018)

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

Bằng 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.
Xuất bản năm 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)

Bằng 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.
Được phát hành 2000

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

Bằng 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.
Xuất bản năm MMWR Morb Mortal Wkly Rep (2020)