Publications by:
Melissa H. Little
Also publishes as (Melissa Little)
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Mallawaarachchi, Amali, Mccarthy, Hugh, Forbes, Thomas A., Jayasinghe, Kushani, Patel, Chirag, Alexander, Stephen I., Boughtwood, Tiffany, Braithwaite, Jeffrey, Chakera, Aron, Crafter, Sam, Deveson, Ira W., Faull, Randall, Harris, Trudie, Johnstone, Lilian, Jose, Matthew, Leaver, Anna, Little, Melissa H., MacArthur, Daniel, Mattiske, Tessa, Mincham, Christine, Nicholls, Kathy, Quinlan, Catherine, Quinn, Michael C.J., Rangan, Gopala, Ryan, Jessica, Simons, Cas, Smyth, Ian, Sundaram, Madhivanan, Trnka, Peter, Wedd, Laura, Biros, Erik, Stark, Zornitza, and Mallett, Andrew (2025) Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocol. BMC Nephrology, 26 (1). 51.
Ryan, Danica, Sutherland, Megan R., Flores, Tracey J., Kent, Alison L., Dahlstrom, Jane E., Puelles, Victor G., Bertram, John F., McMahon, Andrew P., Little, Melissa H., Moore, Lynette, and Black, Mary Jane (2018) Development of the human fetal kidney from mid to late gestation in male and female infants. EBioMedicine, 27. pp. 275-283.
Forbes, Thomas A., Howden, Sara E., Lawlor, Kynan, Phipson, Belinda, Maksimovic, Jovana, Hale, Lorna, Wilson, Sean, Quinlan, Catherine, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Trnka, Peter, Oshlack, Alicia, Patel, Chirag, Mallett, Andrew, Simons, Cas, and Little, Melissa H. (2018) Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms. American Journal of Human Genetics, 102 (5). pp. 816-831.
Mallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, Alexander, Stephen I., Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, Mccarthy, Hugh J., Hyland, Valentine, Hoy, Wendy E., Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy, Helen, and Little, Melissa (2015) A protocol for the identification and validation of novel genetic causes of kidney disease. BMC Nephrology, 16. 152.
