KLHDC8B in Hodgkin lymphoma and possibly twinning

بواسطة Timms, Andrew E, Horwitz, Marshall S
منشور في 2010

Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice

بواسطة Geister, Krista A., Timms, Andrew E., Beier, David R.
الحاوية / القاعدة G3 (Bethesda) (2017)

Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice

بواسطة Ha, Seungshin, Lindsay, Anna M., Timms, Andrew E., Beier, David R.
الحاوية / القاعدة G3 (Bethesda) (2016)

Variant mapping and mutation discovery in inbred mice using next-generation sequencing

بواسطة Gallego-Llamas, Jabier, Timms, Andrew E., Geister, Krista A., Lindsay, Anna, Beier, David R.
الحاوية / القاعدة BMC Genomics (2015)

Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice

بواسطة Gallego-Llamas, Jabier, Timms, Andrew E., Pitstick, Rose, Peters, Janet, Carlson, George A., Beier, David R.
الحاوية / القاعدة PLoS One (2016)

Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus

بواسطة Ruggeri, Gaia, Timms, Andrew E., Cheng, Chi, Weiss, Avery, Kollros, Peter, Chapman, Teresa, Tully, Hannah, Mirzaa, Ghayda M.
الحاوية / القاعدة Am J Med Genet A (2018)

Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature

بواسطة Gao, Juehua, Gentzler, Ryan D, Timms, Andrew E, Horwitz, Marshall S, Frankfurt, Olga, Altman, Jessica K, Peterson, LoAnn C
منشور في 2014

Erratum: Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature

بواسطة Gao, Juehua, Gentzler, Ryan D., Timms, Andrew E., Horwitz, Marshall S., Frankfurt, Olga, Altman, Jessica K., Peterson, LoAnn C.
الحاوية / القاعدة J Hematol Oncol (2015)

The effect of mouse strain, sex and carcinogen dose on toxicity and the development of lung dysplasia and squamous cell carcinomas in mice

بواسطة Riolobos, Laura, Gad, Ekram A., Treuting, Piper M., Timms, Andrew E., Hershberg, Elliot A., Corulli, Lauren R., Rodmaker, Erin, Disis, Mary L.
الحاوية / القاعدة Cancer Prev Res (Phila) (2019)

A Novel Rasopathy Caused by Recurrent De Novo Missense Mutations In PPP1CB Closely Resembles Noonan Syndrome with Loose Anagen Hair

بواسطة Gripp, Karen W., Aldinger, Kimberly A., Bennett, James T., Baker, Laura, Tusi, Jessica, Powell-Hamilton, Nina, Stabley, Deborah, Sol-Church, Katia, Timms, Andrew E., Dobyns, William B.
الحاوية / القاعدة Am J Med Genet A (2016)

Genotype correlates with clinical severity in PIK3CA-associated lymphatic malformations

بواسطة Zenner, Kaitlyn, Cheng, Chi Vicky, Jensen, Dana M., Timms, Andrew E., Shivaram, Giridhar, Bly, Randall, Ganti, Sheila, Whitlock, Kathryn B., Dobyns, William B., Perkins, Jonathan, Bennett, James T.
الحاوية / القاعدة JCI Insight (2019)

Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain

بواسطة Aldinger, Kimberly A., Timms, Andrew E., MacDonald, James W., McNamara, Hanna K., Herstein, Jennifer S., Bammler, Theo K., Evgrafov, Oleg V., Knowles, James A., Levitt, Pat
الحاوية / القاعدة Sci Data (2020)

Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosis

بواسطة Park, Sarah S., Beyer, Richard P., Smyth, Matthew D., Clarke, Christine M., Timms, Andrew E., Bammler, Theo K., Stamper, Brendan D., Mecham, Brigham H., Gustafson, Jennifer A., Cunningham, Michael L.
الحاوية / القاعدة Bone (2015)

Mapping the cis-regulatory architecture of the human retina reveals noncoding genetic variation in disease

بواسطة Cherry, Timothy J., Yang, Marty G., Harmin, David A., Tao, Peter, Timms, Andrew E., Bauwens, Miriam, Allikmets, Rando, Jones, Evan M., Chen, Rui, De Baere, Elfride, Greenberg, Michael E.
الحاوية / القاعدة Proc Natl Acad Sci U S A (2020)

MYT1 role in the microtia‐craniofacial microsomia spectrum

بواسطة Luquetti, Daniela V., Heike, Carrie L., Zarante, Ignacio, Timms, Andrew E., Gustafson, Jonas, Pachajoa, Harry, Porras‐Hurtado, Gloria L., Ayala‐Ramirez, Paola, Duenas‐Roque, Milagros M., Jimenez, Natalia, Ibanez, Lina M., Hurtado‐Villa, Paula
الحاوية / القاعدة Mol Genet Genomic Med (2020)

Single Suture Craniosynostosis: Identification of Rare Variants in Genes Associated with Syndromic Forms

بواسطة Clarke, Christine M., Fok, Vincent T., Gustafson, Jennifer A., Smyth, Matthew D., Timms, Andrew E., Frazar, Chris D., Smith, Joshua D., Birgfeld, Craig B., Lee, Amy, Ellenbogen, Richard, Gruss, Joseph S., Hopper, Richard A., Cunningham, Michael L.
الحاوية / القاعدة Am J Med Genet A (2017)

The Interleukin 1 Gene Cluster Contains a Major Susceptibility Locus for Ankylosing Spondylitis

بواسطة Timms, Andrew E., Crane, Alison M., Sims, Anne-Marie, Cordell, Heather J., Bradbury, Linda A., Abbott, Aaron, Coyne, Mark R. E., Beynon, Owen, Herzberg, Ibi, Duff, Gordon W., Calin, Andrei, Cardon, Lon R., Wordsworth, B. Paul, Brown, Matthew A.
منشور في 2004

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly

بواسطة Di Donato, Nataliya, Timms, Andrew E., Aldinger, Kimberly A., Mirzaa, Ghayda M., Bennett, James T., Collins, Sarah, Olds, Carissa, Mei, Davide, Chiari, Sara, Carvill, Gemma, Myers, Candace T., Rivière, Jean-Baptiste, Zaki, Maha S., Gleeson, Joseph G., Rump, Andreas, Conti, Valerio, Parrini, Elena, Ross, M. Elizabeth, Ledbetter, David H., Guerrini, Renzo, Dobyns, William B.
الحاوية / القاعدة Genet Med (2018)

Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum

بواسطة Haldipur, Parthiv, Aldinger, Kimberly A., Bernardo, Silvia, Deng, Mei, Timms, Andrew E., Overman, Lynne M., Winter, Conrad, Lisgo, Steven N., Razavi, Ferechte, Silvestri, Evelina, Manganaro, Lucia, Adle-Biasette, Homa, Guilmiot, Fabien, Russo, Rosa, Kidron, Debora, Hof, Patrick R., Gerrelli, Dianne, Lindsay, Susan J., Dobyns, William B., Glass, Ian A., Alexandre, Paula, Millen, Kathleen J.
الحاوية / القاعدة Science (2019)

Characterization of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next generation sequencing study

بواسطة Mirzaa, Ghayda, Conti, Valerio, Timms, Andrew E., Smyser, Christopher D., Ahmed, Sarah, Carter, Melissa, Barnett, Sarah, Hufnagel, Robert B., Goldstein, Amy, Narumi-Kishimoto, Yoko, Olds, Carissa, Collins, Sarah, Johnston, Kathreen, Deleuze, Jean-François, Nitschké, Patrick, Friend, Kathryn, Harris, Catharine, Goetsch, Allison, Martin, Beth, Boyle, Evan August, Parrini, Elena, Mei, Davide, Tattini, Lorenzo, Slavotinek, Anne, Blair, Ed, Barnett, Christopher, Shendure, Jay, Chelly, Jamel, Dobyns, William B., Guerrini, Renzo
الحاوية / القاعدة Lancet Neurol (2015)