Glycerol Hypersensitivity in a Drosophila Model for Glycerol Kinase Deficiency Is Affected by Mutations in Eye Pigmentation Genes

le Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Foilsithe 2012

Disruption of Glycerol Metabolism by RNAi Targeting of Genes Encoding Glycerol Kinase Results in a Range of Phenotype Severity in Drosophila

le Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Foilsithe 2013

Genetic Screening in Patients with Craniofacial Malformations

le Yoon, Amanda J., Pham, Binh N., Dipple, Katrina M.
Foilsithe in J Pediatr Genet (2016)

Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis

le Kohannim, Omid, Peredo, Jane, Dipple, Katrina M., Quintero-Rivera, Fabiola
Foilsithe 2011

Moonlighting function of glycerol kinase causes systems-level changes in rat hepatoma cells

le Sriram, Ganesh, Parr, Lilly S., Rahib, Lola, Liao, James C., Dipple, Katrina M.
Foilsithe 2010

Transcriptomic and network component analysis of glycerol kinase in skeletal muscle using a mouse model of glycerol kinase deficiency

le Rahib, Lola, Sriram, Ganesh, Harada, Melissa K., Liao, James C., Dipple, Katrina M.
Foilsithe 2009

Ensemble Modeling of Hepatic Fatty Acid Metabolism with a Synthetic Glyoxylate Shunt

le Dean, Jason T., Rizk, Matthew L., Tan, Yikun, Dipple, Katrina M., Liao, James C.
Foilsithe 2010

Mathematical Modeling of the Insulin Signal Transduction Pathway for Prediction of Insulin Sensitivity from Expression Data

le Ho, Clark K, Rahib, Lola, Liao, James C, Sriram, Ganesh, Dipple, Katrina M
Foilsithe in Mol Genet Metab (2014)

Suicide Risk in Adolescents with Fetal Alcohol Spectrum Disorders

le O’Connor, Mary J., Portnoff, Larissa C., Lebsack-Coleman, Michael, Dipple, Katrina M.
Foilsithe in Birth Defects Res (2019)

Gestational diabetes associated with a novel mutation (378–379insTT) in the glycerol kinase gene

le Zhang, Yao H., Van Hove, Johan L., McCabe, Edward R.B., Dipple, Katrina M.
Foilsithe in Mol Genet Metab Rep (2015)

Modeling craniofacial and skeletal congenital birth defects to advance therapies

le Neben, Cynthia L., Roberts, Ryan R., Dipple, Katrina M., Merrill, Amy E., Klein, Ophir D.
Foilsithe in Hum Mol Genet (2016)

Single-Gene Disorders: What Role Could Moonlighting Enzymes Play?

le Sriram, Ganesh, Martinez, Julian A., McCabe, Edward R. B., Liao, James C., Dipple, Katrina M.
Foilsithe 2005

Resistance to Diet-Induced Obesity in Mice with Synthetic Glyoxylate Shunt

le Dean, Jason T., Tran, Linh, Beaven, Simon, Tontonoz, Peter, Reue, Karen, Dipple, Katrina M., Liao, James C.
Foilsithe in Cell Metab (2009)

Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome

le Yazdani, Shahram, Badjatiya, Anish, Dorrani, Naghmeh, Lee, Hane, Grody, Wayne W., Nelson, Stanley F., Dipple, Katrina M.
Foilsithe in Mol Genet Metab Rep (2020)

Global Metabolic Effects of Glycerol Kinase Overexpression in Rat Hepatoma Cells

le Sriram, Ganesh, Rahib, Lola, He, Jian-Sen, Campos, Allison E., Parr, Lilly S., Liao, James C., Dipple, Katrina M.
Foilsithe 2007

Development of catecholamine and cortisol stress responses in zebrafish()()

le Eto, Kaoru, Mazilu-Brown, Jaime K., Henderson-MacLennan, Nicole, Dipple, Katrina M., McCabe, Edward R.B.
Foilsithe in Mol Genet Metab Rep (2014)

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

le Lee, Hane, Deignan, Joshua L., Dorrani, Naghmeh, Strom, Samuel P., Kantarci, Sibel, Quintero-Rivera, Fabiola, Das, Kingshuk, Toy, Traci, Harry, Bret, Yourshaw, Michael, Fox, Michelle, Fogel, Brent L., Martinez-Agosto, Julian A., Wong, Derek A., Chang, Vivian Y., Shieh, Perry B., Palmer, Christina G. S., Dipple, Katrina M., Grody, Wayne W., Vilain, Eric, Nelson, Stanley F.
Foilsithe in JAMA (2014)

The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children

le Freed, Amanda S., Candadai, Sarah V. Clowes, Sikes, Megan C., Thies, Jenny, Byers, Heather M., Dines, Jennifer N., Ndugga-Kabuye, Mesaki Kenneth, Smith, Mallory B., Fogus, Katie, Mefford, Heather C., Lam, Christina, Adam, Margaret P., Sun, Angela, McGuire, John K., DiGeronimo, Robert, Dipple, Katrina M., Deutsch, Gail H., Billimoria, Zeenia C., Bennett, James T.
Foilsithe in J Pediatr (2020)

Validation of Candidate Causal Genes for Abdominal Obesity Which Affect Shared Metabolic Pathways and Networks

le Yang, Xia, Deignan, Joshua L., Qi, Hongxiu, Zhu, Jun, Qian, Su, Zhong, Judy, Torosyan, Gevork, Majid, Sana, Falkard, Brie, Kleinhanz, Robert R., Karlsson, Jenny, Castellani, Lawrence W., Mumick, Sheena, Wang, Kai, Xie, Tao, Coon, Michael, Zhang, Chunsheng, Estrada-Smith, Daria, Farber, Charles R., Wang, Susanna S., Van Nas, Atila, Ghazalpour, Anatole, Zhang, Bin, MacNeil, Douglas J., Lamb, John R., Dipple, Katrina M., Reitman, Marc L., Mehrabian, Margarete, Lum, Pek Y., Schadt, Eric E., Lusis, Aldons J., Drake, Thomas A.
Foilsithe 2009

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update

le Huang, Lijia, Vanstone, Megan R., Hartley, Taila, Osmond, Matthew, Barrowman, Nick, Allanson, Judith, Baker, Laura, Dabir, Tabib A., Dipple, Katrina M., Dobyns, William B., Estrella, Jane, Faghfoury, Hanna, Favaro, Francine P., Goel, Himanshu, Gregersen, Pernille A., Gripp, Karen W., Grix, Art, Guion-Almeida, Maria-Leine, Harr, Margaret H., Hudson, Cindy, Hunter, Alasdair G.W., Johnson, John, Joss, Shelagh K., Kimball, Amy, Kini, Usha, Kline, Antonie D., Lauzon, Julie, Lildballe, Dorte L., López-González, Vanesa, Martinezmoles, Johanna, Meldrum, Cliff, Mirzaa, Ghayda M., Morel, Chantal F., Morton, Jenny E.V., Pyle, Louise C., Quintero-Rivera, Fabiola, Richer, Julie, Scheuerle, Angela E., Schönewolf-Greulich, Bitten, Shears, Deborah J., Silver, Josh, Smith, Amanda C., Temple, I. Karen, van de Kamp, Jiddeke M., van Dijk, Fleur S., Vandersteen, Anthony M., White, Sue M., Zackai, Elaine H., Zou, Ruobing, Bulman, Dennis E., Boycott, Kym M., Lines, Matthew A.
Foilsithe in Hum Mutat (2015)