Updated national birth prevalence estimates for selected birth defects in the United States, 2004-2006 von Parker, Samantha E., Mai, Cara T., Canfield, Mark A., Rickard, Russel, Wang, Ying, Meyer, Robert E., Anderson, Patrick, Mason, Craig A., Collins, Julianne S., Kirby, Russell S., Correa, Adolfo

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United States Head Circumference Growth Reference Charts: Birth to 21 Years von Rollins, Jonathan D., BS, Collins, Julianne S., PhD, Holden, Kenton R., MD

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National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999-2001 von Canfield, Mark A., Honein, Margaret A., Yuskiv, Nataliya, Xing, Jian, Mai, Cara T., Collins, Julianne S., Devine, Owen, Petrini, Joann, Ramadhani, Tunu A., Hobbs, Charlotte A., Kirby, Russell S.

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Trends in the postfortification prevalence of spina bifida and anencephaly in the United States von Boulet, Sheree L., Yang, Quanhe, Mai, Cara, Kirby, Russell S., Collins, Julianne S., Robbins, James M., Meyer, Robert, Canfield, Mark A., Mulinare, Joe

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Quantitative standards for fetal and neonatal autopsy von ARCHIE, John G, COLLINS, Julianne S, LEBEL, Robert Roger

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Prevalence, Incidence, and Etiology of Epilepsies in Rural Honduras: The Salamá Study von Medina, Marco T., Durón, Reyna M., Martínez, Lisandro, Osorio, Juan Ramón, Estrada, Ana L., Zúniga, Concepción, Cartagena, Dora, Collins, Julianne S., Holden, Kenton R.

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Long Term Maintenance of Neural Tube Defects Prevention in a High Prevalence State von Collins, Julianne S., PhD, Atkinson, Kristy K., BS, Dean, Jane H., RN, Best, Robert G., PhD, Stevenson, Roger E., MD

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Economic Evaluation of a Neural Tube Defect Recurrence–Prevention Program von Grosse, Scott D., PhD, Ouyang, Lijing, PhD, Collins, Julianne S., PhD, Green, Denise, MPH, Dean, Jane H., RN, Stevenson, Roger E., MD

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Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders von Boccuto, Luigi, Lauri, Maria, Sarasua, Sara M, Skinner, Cindy D, Buccella, Daniela, Dwivedi, Alka, Orteschi, Daniela, Collins, Julianne S, Zollino, Marcella, Visconti, Paola, Dupont, Barb, Tiziano, Danilo, Schroer, Richard J, Neri, Giovanni, Stevenson, Roger E, Gurrieri, Fiorella, Schwartz, Charles E

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Association between deletion size and important phenotypes expands the genomic region of interest in Phelan–McDermid syndrome (22q13 deletion syndrome) von Sarasua, Sara M, Dwivedi, Alka, Boccuto, Luigi, Rollins, Jonathan D, Chen, Chin-Fu, Rogers, R Curtis, Phelan, Katy, DuPont, Barbara R, Collins, Julianne S

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22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan–McDermid syndrome von Sarasua, Sara M., Dwivedi, Alka, Boccuto, Luigi, Chen, Chin-Fu, Sharp, Julia L., Rollins, Jonathan D., Collins, Julianne S., Rogers, R. Curtis, Phelan, Katy, DuPont, Barbara R.

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Folic acid supplementation and neural tube defect recurrence prevention von Grosse, Scott D., Collins, Julianne S.

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Detecting Polymorphisms and Mutations in Candidate Genes von Collins, Julianne S., Schwartz, Charles E.

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Survival of Infants With Neural Tube Defects in the Presence of Folic Acid Fortification von Bol, Kirk A, Collins, Julianne S, Kirby, Russell S, National Birth Defects Prevention Network

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Reduction in rate of epilepsy from neurocysticercosis by community interventions: The Salamá, Honduras Study von Medina, Marco T., Aguilar‐Estrada, Rafael L., Alvarez, Allan, Durón, Reyna M., Martínez, Lizandro, Dubón, Sofia, Estrada, Ana L., Zúniga, Concepción, Cartagena, Dora, Thompson, Arnold, Ramirez, Eunice, Banegas, Lenín, Osorio, Juan R., Delgado‐Escueta, Antonio V., Collins, Julianne S., Holden, Kenton R.

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The role of TNF and its receptors in Alzheimer’s disease von Perry, Rodney T, Collins, Julianne S, Wiener, Howard, Acton, Ronald, Go, Rodney C.P

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Results of a high-resolution genome screen of 437 Alzheimer's Disease families von Blacker, Deborah, Bertram, Lars, Saunders, Aleister J., Moscarillo, Thomas J., Albert, Marilyn S., Wiener, Howard, Perry, Rodney T., Collins, Julianne S., Harrell, Lindy E., Go, Rodney C.P., Mahoney, Amy, Beaty, Terri, Fallin, M. Danielle, Avramopoulos, Dimitrios, Chase, Gary A., Folstein, Marshal F., McInnis, Melvin G., Bassett, Susan S., Doheny, Kimberly J., Pugh, Elizabeth W., Tanzi, Rudolph E.

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Changes in the birth prevalence of selected birth defects after grain fortification with folic acid in the United States : Findings from a multi-state population-based study von CANFIELD, Mark A, COLLINS, Julianne S, BOTTO, Lorenzo D, WILLIAMS, Laura J, MAI, Cara T, KIRBY, Russell S, PEARSON, Kay, DEVINE, Owen, MULINARE, Joe

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Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder von Jackson, Pamela B., Boccuto, Luigi, Skinner, Cindy, Collins, Julianne S., Neri, Giovanni, Gurrieri, Fiorella, Schwartz, Charles E.

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Birth defects surveillance, epidemiology, and public health von Kirby, Russell S., Collins, Julianne S.

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