Limiting the Extent of the RDN1 Heterochromatin Domain by a Silencing Barrier and Sir2 Protein Levels in Saccharomyces cerevisiae

nork Biswas, Moumita, Maqani, Nazif, Rai, Ragini, Kumaran, Srikala P., Iyer, Kavitha R., Sendinc, Erdem, Smith, Jeffrey S., Laloraya, Shikha
Argitaratua 2009

Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders

nork Szot, Justin O., Campagnolo, Carla, Cao, Ye, Iyer, Kavitha R., Cuny, Hartmut, Drysdale, Thomas, Flores-Daboub, Josue A., Bi, Weimin, Westerfield, Lauren, Liu, Pengfei, Leung, Tse Ngong, Choy, Kwong Wai, Chapman, Gavin, Xiao, Rui, Siu, Victoria M., Dunwoodie, Sally L.
Argitaratua izan da Am J Hum Genet (2020)

Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants

nork Chapman, Gavin, Moreau, Julie L M, I P, Eddie, Szot, Justin O, Iyer, Kavitha R, Shi, Hongjun, Yam, Michelle X, O’Reilly, Victoria C, Enriquez, Annabelle, Greasby, Joelene A, Alankarage, Dimuthu, Martin, Ella M M A, Hanna, Bernadette C, Edwards, Matthew, Monger, Steven, Blue, Gillian M, Winlaw, David S, Ritchie, Helen E, Grieve, Stuart M, Giannoulatou, Eleni, Sparrow, Duncan B, Dunwoodie, Sally L
Argitaratua izan da Hum Mol Genet (2020)

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

nork Martin, Ella M M A, Enriquez, Annabelle, Sparrow, Duncan B, Humphreys, David T, McInerney-Leo, Aideen M, Leo, Paul J, Duncan, Emma L, Iyer, Kavitha R, Greasby, Joelene A, Ip, Eddie, Giannoulatou, Eleni, Sheng, Delicia, Wohler, Elizabeth, Dimartino, Clémantine, Amiel, Jeanne, Capri, Yline, Lehalle, Daphné, Mory, Adi, Wilnai, Yael, Lebenthal, Yael, Gharavi, Ali G, Krzemień, Grażyna G, Miklaszewska, Monika, Steiner, Robert D, Raggio, Cathy, Blank, Robert, Baris Feldman, Hagit, Milo Rasouly, Hila, Sobreira, Nara L M, Jobling, Rebekah, Gordon, Christopher T, Giampietro, Philip F, Dunwoodie, Sally L, Chapman, Gavin
Argitaratua izan da Hum Mol Genet (2020)