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

av Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Publicerad 2012

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

av Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Publicerad 2013

Genetic Screening in Patients with Craniofacial Malformations

av Yoon, Amanda J., Pham, Binh N., Dipple, Katrina M.
I publikationen 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

av Kohannim, Omid, Peredo, Jane, Dipple, Katrina M., Quintero-Rivera, Fabiola
Publicerad 2011

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

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

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

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

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

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

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

av Ho, Clark K, Rahib, Lola, Liao, James C, Sriram, Ganesh, Dipple, Katrina M
I publikationen Mol Genet Metab (2014)

Suicide Risk in Adolescents with Fetal Alcohol Spectrum Disorders

av O’Connor, Mary J., Portnoff, Larissa C., Lebsack-Coleman, Michael, Dipple, Katrina M.
I publikationen Birth Defects Res (2019)

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

av Zhang, Yao H., Van Hove, Johan L., McCabe, Edward R.B., Dipple, Katrina M.
I publikationen Mol Genet Metab Rep (2015)

Modeling craniofacial and skeletal congenital birth defects to advance therapies

av Neben, Cynthia L., Roberts, Ryan R., Dipple, Katrina M., Merrill, Amy E., Klein, Ophir D.
I publikationen Hum Mol Genet (2016)

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

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

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

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

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

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

Global Metabolic Effects of Glycerol Kinase Overexpression in Rat Hepatoma Cells

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

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

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

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

av 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.
I publikationen JAMA (2014)

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

av 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.
I publikationen J Pediatr (2020)

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

av 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.
Publicerad 2009

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update

av 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.
I publikationen Hum Mutat (2015)