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

od Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Wydane 2012

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

od Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Wydane 2013

Genetic Screening in Patients with Craniofacial Malformations

od Yoon, Amanda J., Pham, Binh N., Dipple, Katrina M.
Wydane w 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

od Kohannim, Omid, Peredo, Jane, Dipple, Katrina M., Quintero-Rivera, Fabiola
Wydane 2011

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

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

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

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

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

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

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

od Ho, Clark K, Rahib, Lola, Liao, James C, Sriram, Ganesh, Dipple, Katrina M
Wydane w Mol Genet Metab (2014)

Suicide Risk in Adolescents with Fetal Alcohol Spectrum Disorders

od O’Connor, Mary J., Portnoff, Larissa C., Lebsack-Coleman, Michael, Dipple, Katrina M.
Wydane w Birth Defects Res (2019)

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

od Zhang, Yao H., Van Hove, Johan L., McCabe, Edward R.B., Dipple, Katrina M.
Wydane w Mol Genet Metab Rep (2015)

Modeling craniofacial and skeletal congenital birth defects to advance therapies

od Neben, Cynthia L., Roberts, Ryan R., Dipple, Katrina M., Merrill, Amy E., Klein, Ophir D.
Wydane w Hum Mol Genet (2016)

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

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

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

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

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

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

Global Metabolic Effects of Glycerol Kinase Overexpression in Rat Hepatoma Cells

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

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

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

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

od 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.
Wydane w JAMA (2014)

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

od 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.
Wydane w J Pediatr (2020)

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

od 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.
Wydane 2009

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update

od 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.
Wydane w Hum Mutat (2015)