CAFFEINE INTAKE AND RISK OF NEURAL TUBE DEFECTS: AUTHOR RESPONSE TO CORRESPONDENCE

Por Schmidt, Rebecca J., Browne, Marilyn L., Pessah, Isaac N.
Publicado no Birth Defects Res A Clin Mol Teratol (2010)

Unintentional drownings among New York State residents, 1988-1994.

Por Browne, Marilyn L., Lewis-Michl, Elizabeth L., Stark, Alice D.
Publicado em 2003

Watercraft-related drownings among New York State residents, 1988-1994.

Por Browne, Marilyn L., Lewis-Michl, Elizabeth L., Stark, Alice D.
Publicado em 2003

Caffeine, Selected Metabolic Gene Variants, and Risk for Neural Tube Defects

Por Schmidt, Rebecca J., Romitti, Paul A., Burns, Trudy L., Murray, Jeffrey C., Browne, Marilyn L., Druschel, Charlotte M., Olney, Richard S.
Publicado em 2010

Maternal Caffeine Consumption and Risk of Congenital Limb Deficiencies

Por Chen, Lei, Bell, Erin M., Browne, Marilyn L., Druschel, Charlotte M., Romitti, Paul A., Schmidt, Rebecca J., Burns, Trudy L., Moslehi, Roxana, Olney, Richard S.
Publicado no Birth Defects Res A Clin Mol Teratol (2012)

Maternal Autoimmune Disease and Birth Defects in the National Birth Defects Prevention Study

Por Howley, Meredith M., Browne, Marilyn L., Van Zutphen, Alissa R., Richardson, Sandra D., Blossom, Sarah J., Broussard, Cheryl S., Carmichael, Suzan L., Druschel, Charlotte M.
Publicado no Birth Defects Res A Clin Mol Teratol (2016)

Next steps for birth defects research and prevention: The Birth Defects Study To Evaluate Pregnancy exposureS (BD-STEPS)

Por Tinker, Sarah C., Carmichael, Suzan L., Anderka, Marlene, Browne, Marilyn L., Caspers Conway, Kristin M., Meyer, Robert E., Nembhard, Wendy N., Olney, Richard S., Reefhuis, Jennita
Publicado no Birth Defects Res A Clin Mol Teratol (2015)

Prevalence and Clinical Attributes of Congenital Microcephaly — New York, 2013–2015

Por Graham, Krishika A., Fox, Deborah J., Talati, Achala, Pantea, Cristian, Brady, Laura, Carter, Sondra L., Friedenberg, Eric, Vora, Neil M., Browne, Marilyn L., Lee, Christopher T.
Publicado no MMWR Morb Mortal Wkly Rep (2017)

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 em 2012

Hirschsprung’s disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation

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

Anorectal atresia and variants at predicted regulatory sites in candidate genes

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

Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways

Por Sicko, Robert J., Browne, Marilyn L., Rigler, Shannon L., Druschel, Charlotte M., Liu, Gang, Fan, Ruzong, Romitti, Paul A., Caggana, Michele, Kay, Denise M., Brody, Lawrence C., Mills, James L.
Publicado no PLoS One (2016)

Rare Copy Number Variants in a Population Based Investigation of Hypoplastic Right Heart Syndrome

Por Dimopoulos, Aggeliki, Sicko, Robert J., Kay, Denise M., Rigler, Shannon L., Druschel, Charlotte M., Caggana, Michele, Browne, Marilyn L., Fan, Ruzong, Romitti, Paul A., Brody, Lawrence C., Mills, James L.
Publicado no Birth Defects Res (2017)

Antihypertensive Medication Use During Pregnancy and the Risk of Cardiovascular Malformations

Por Caton, Alissa R., Bell, Erin M., Druschel, Charlotte M., Werler, Martha M., Lin, Angela E., Browne, Marilyn L., McNutt, Louise-Anne, Romitti, Paul A., Mitchell, Allen A., Olney, Richard S., Correa, Adolfo
Publicado no Hypertension (2009)

Copy-number variants and candidate gene mutations in isolated split hand/foot malformation

Por Carter, Tonia C., Sicko, Robert J., Kay, Denise M., Browne, Marilyn L., Romitti, Paul A., Edmunds, Zoë L., Liu, Aiyi, Fan, Ruzong, Druschel, Charlotte M., Caggana, Michele, Brody, Lawrence C., Mills, James L.
Publicado no J Hum Genet (2017)

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects

Por Pangilinan, Faith, Molloy, Anne M, Mills, James L, Troendle, James F, Parle-McDermott, Anne, Kay, Denise M, Browne, Marilyn L, McGrath, Emily C, Abaan, Hatice Ozel, Sutton, Marie, Kirke, Peadar N, Caggana, Michele, Shane, Barry, Scott, John M, Brody, Lawrence C
Publicado no BMC Med Genet (2014)

The National Birth Defects Prevention Study: a review of the methods

Por Reefhuis, Jennita, Gilboa, Suzanne M., Anderka, Marlene, Browne, Marilyn L., Feldkamp, Marcia L., Hobbs, Charlotte A., Jenkins, Mary M., Langlois, Peter H., Newsome, Kimberly B., Olshan, Andrew F., Romitti, Paul A., Shapira, Stuart K., Shaw, Gary M., Tinker, Sarah C., Honein, Margaret A.
Publicado no Birth Defects Res A Clin Mol Teratol (2015)

Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways

Por Hagen, Erin M., Sicko, Robert J., Kay, Denise M., Rigler, Shannon L., Dimopoulos, Aggeliki, Ahmad, Shabbir, Doleman, Margaret H., Fan, Ruzong, Romitti, Paul A., Browne, Marilyn L., Caggana, Michele, Brody, Lawrence C., Shaw, Gary M., Jelliffe-Pawlowski, Laura L., Mills, James L.
Publicado no Hum Genet (2016)

Population-Based Microcephaly Surveillance in the United States, 2009 to 2013: An Analysis of Potential Sources of Variation

Por Cragan, Janet D., Isenburg, Jennifer L., Parker, Samantha E., Alverson, C.J., Meyer, Robert E., Stallings, Erin B., Kirby, Russell S., Lupo, Philip J., Liu, Jennifer S., Seagroves, Amanda, Ethen, Mary K., Cho, Sook Ja, Evans, MaryAnn, Liberman, Rebecca F., Fornoff, Jane, Browne, Marilyn L., Rutkowski, Rachel E., Nance, Amy E., Anderka, Marlene, Fox, Deborah J., Steele, Amy, Copeland, Glenn, Romitti, Paul A., Mai, Cara T.
Publicado no Birth Defects Res A Clin Mol Teratol (2016)