Large ABCA3 and SFTPC Deletions Resulting in Lung Disease

Por Henderson, Lindsay B., Melton, Kristin, Wert, Susan, Couriel, Jonathan, Bush, Andrew, Ashworth, Michael, Nogee, Lawrence M.
Publicado em 2013

Genomic Changes in Gliomas Detected Using Single Nucleotide Polymorphism Array in Formalin-Fixed, Paraffin-Embedded Tissue: Superior Results Compared with Microsatellite Analysis

Por Harada, Shuko, Henderson, Lindsay B., Eshleman, James R., Gocke, Christopher D., Burger, Peter, Griffin, Constance A., Batista, Denise A.S.
Publicado em 2011

First Trimester Diagnosis of Holoprosencephaly Secondary to a Ring Chromosome 7

Por Henderson, Lindsay B., Corson, Virginia L., Saul, Daniel O., Anderson, Cynthia, Millard, Sarah, Batista, Denise A. S., Blakemore, Karin J., DeScipio, Cheryl
Publicado em 2013

Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients

Por Green, Deanna M, McDougal, Kathryn E, Blackman, Scott M, Sosnay, Patrick R, Henderson, Lindsay B, Naughton, Kathleen M, Collaco, J Michael, Cutting, Garry R
Publicado em 2010

Variation in MSRA Modifies Risk of Neonatal Intestinal Obstruction in Cystic Fibrosis

Por Henderson, Lindsay B., Doshi, Vishal K., Blackman, Scott M., Naughton, Kathleen M., Pace, Rhonda G., Moskovitz, Jackob, Knowles, Michael R., Durie, Peter R., Drumm, Mitchell L., Cutting, Garry R.
Publicado em 2012

Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis

Por McDougal, Kathryn E, Green, Deanna M, Vanscoy, Lori L, Fallin, M Daniele, Grow, Michael, Cheng, Suzanne, Blackman, Scott M, Collaco, J Michael, Henderson, Lindsay B, Naughton, Kathleen, Cutting, Garry R
Publicado em 2010

De Novo Missense Variants in PPP2R5D Are Associated with Intellectual Disability, Macrocephaly, Hypotonia, and Autism

Por Shang, Linshan, Henderson, Lindsay B., Cho, Megan T., Petrey, Donald S., Fong, Chin-To, Haude, Katrina M., Shur, Natasha, Lundberg, Julie, Hauser, Natalie, Carmichael, Jason, Innis, Jeffrey, Schuette, Jane, Wu, Yvonne W., Asaikar, Shailesh, Pearson, Margaret, Folk, Leandra, Retterer, Kyle, Monaghan, Kristin G., Chung, Wendy K.
Publicado no Neurogenetics (2015)

Mutations in HIVEP2 are associated with developmental delay, intellectual disability and dysmorphic features

Por Steinfeld, Hallie, Cho, Megan T., Retterer, Kyle, Person, Rick, Schaefer, G. Bradley, Danylchuk, Noelle, Malik, Saleem, Wechsler, Stephanie Burns, Wheeler, Patricia G., van Gassen, Koen L.I., Terhal, P.A., Verhoeven, Virginie J.M., van Slegtenhorst, Marjon A., Monaghan, Kristin G., Henderson, Lindsay B., Chung, Wendy K.
Publicado no Neurogenetics (2016)

IFRD1 polymorphisms in cystic fibrosis with potential link to altered neutrophil function

Por Gu, YuanYuan, Harley, Isaac T. W., Henderson, Lindsay B., Aronow, Bruce J., Vietor, Ilja, Huber, Lukas A., Harley, John B., Kilpatrick, Jeffrey R., Langefeld, Carl D., Williams, Adrienne H., Jegga, Anil G., Chen, Jing, Wills-Karp, Marsha, Arshad, S. Hasan, Ewart, Susan L., Thio, Chloe L., Flick, Leah M., Filippi, Marie-Dominique, Grimes, H. Leighton, Drumm, Mitchell L., Cutting, Garry R., Knowles, Michael R., Karp, Christopher L.
Publicado em 2009