All you ever needed to explain genetics to non-geneticists

nork Collins, Amanda
Argitaratua izan da Eur J Hum Genet (2015)

A classic textbook which will earn its space on your bookshelf

nork Collins, Amanda
Argitaratua izan da Eur J Hum Genet (2015)

Conceptualizing anhedonias and implications for depression treatments

nork Winer, E Samuel, Jordan, D Gage, Collins, Amanda C
Argitaratua izan da Psychol Res Behav Manag (2019)

A 117-kb Microdeletion Removing HOXD9–HOXD13 and EVX2 Causes Synpolydactyly

nork Goodman, Frances R., Majewski, Frank, Collins, Amanda L., Scambler, Peter J.
Argitaratua 2002

Egg masses as training aids for spotted lanternfly Lycorma delicatula detection dogs

nork Essler, Jennifer L., Kane, Sarah A., Collins, Amanda, Ryder, Kaley, DeAngelo, Annemarie, Kaynaroglu, Patricia, Otto, Cynthia M.
Argitaratua izan da PLoS One (2021)

1251. Determinants of Infection at a Nontransplanting Cardiothoracic LVAD Program

nork Milgrom, Alexander, Collins, Amanda, Grubbs, J Aaron, Derrick, Caroline, Logan, Kristin, Edelson, William, Branham, Stephany, Mardis, Andrew, Martin, Jeffrey, Weissman, Sharon
Argitaratua izan da Open Forum Infect Dis (2019)

Quantification of transmission risk in a male patient with a FLNB mosaic mutation causing Larsen syndrome: Implications for genetic counseling in postzygotic mosaicism cases

nork Bernkopf, Marie, Hunt, David, Koelling, Nils, Morgan, Tim, Collins, Amanda L., Fairhurst, Joanna, Robertson, Stephen P., Douglas, Andrew G. L., Goriely, Anne
Argitaratua izan da Hum Mutat (2017)

Inherited 2q23.1 microdeletions involving the MBD5 locus

nork Tadros, Shereen, Wang, Rubin, Waters, Jonathan J., Waterman, Christine, Collins, Amanda L., Collinson, Morag N., Ahn, Joo W., Josifova, Dragana, Chetan, Ravi, Kumar, Ajith
Argitaratua izan da Mol Genet Genomic Med (2017)

704. Evaluation of Risk Factors and Outcomes of Early Left Ventricular Assist Device Infections

nork Shealy, Stephanie, Milgrom, Alexander, burns, Stephen, Ferraro, Hunter, Collins, Amanda, Cox, Jenna, Derrick, Caroline, Mardis, Andrew, Grubbs, James, Weissman, Sharon, Justo, Julie Ann, Bookstaver, P B
Argitaratua izan da Open Forum Infect Dis (2020)

CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila

nork Zweier, Christiane, de Jong, Eiko K., Zweier, Markus, Orrico, Alfredo, Ousager, Lilian B., Collins, Amanda L., Bijlsma, Emilia K., Oortveld, Merel A.W., Ekici, Arif B., Reis, André, Schenck, Annette, Rauch, Anita
Argitaratua 2009

The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services

nork Evans, D Gareth R, Barwell, Julian, Eccles, Diana M, Collins, Amanda, Izatt, Louise, Jacobs, Chris, Donaldson, Alan, Brady, Angela F, Cuthbert, Andrew, Harrison, Rachel, Thomas, Sue, Howell, Anthony, Miedzybrodzka, Zosia, Murray, Alex
Argitaratua izan da Breast Cancer Res (2014)

A neurovascular high-frequency optical coherence tomography system enables in situ cerebrovascular volumetric microscopy

nork Ughi, Giovanni J., Marosfoi, Miklos G., King, Robert M., Caroff, Jildaz, Peterson, Lindsy M., Duncan, Benjamin H., Langan, Erin T., Collins, Amanda, Leporati, Anita, Rousselle, Serge, Lopes, Demetrius K., Gounis, Matthew J., Puri, Ajit S.
Argitaratua izan da Nat Commun (2020)

The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth

nork Lynch, Sally Ann, Foulds, Nicola, Thuresson, Ann-Charlotte, Collins, Amanda L, Annerén, Göran, Hedberg, Bernt-Oves, Delaney, Carol A, Iremonger, James, Murray, Caroline M, Crolla, John A, Costigan, Colm, Lam, Wayne, Fitzpatrick, David R, Regan, Regina, Ennis, Sean, Sharkey, Freddie
Argitaratua 2011

3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome

nork Willatt, Lionel , Cox, James , Barber, John , Cabanas, Elisabet Dachs , Collins, Amanda , Donnai, Dian , FitzPatrick, David R. , Maher, Eddy , Martin, Howard , Parnau, Josep , Pindar, Lesley , Ramsay, Jacqueline , Shaw-Smith, Charles , Sistermans, Erik A. , Tettenborn, Michael , Trump, Dorothy , de Vries, Bert B. A. , Walker, Kate , Raymond, F. Lucy 
Argitaratua 2005

Comparative PRKAR1A genotype–phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice

nork Veugelers, Mark, Wilkes, David, Burton, Kimberly, McDermott, Deborah A., Song, Yan, Goldstein, Marsha M., La Perle, Krista, Vaughan, Carl J., O'Hagan, Art, Bennett, Kenneth R., Meyer, Beat J., Legius, Eric, Karttunen, Mervi, Norio, Reijo, Kaariainen, Helena, Lavyne, Michael, Neau, Jean-Philippe, Richter, Gert, Kirali, Kaan, Farnsworth, Alan, Stapleton, Karen, Morelli, Peter, Takanashi, Yoshinori, Bamforth, John-Steven, Eitelberger, Franz, Noszian, Irene, Manfroi, Waldimiro, Powers, James, Mochizuki, Yoshihiko, Imai, Tsuneo, Ko, Gary T. C., Driscoll, Deborah A., Goldmuntz, Elizabeth, Edelberg, Jay M., Collins, Amanda, Eccles, Diana, Irvine, Alan D., McKnight, G. Stanley, Basson, Craig T.
Argitaratua 2004

Intratumoral injection of Clostridium novyi-NT spores induces antitumor responses

nork Roberts, Nicholas J., Zhang, Linping, Janku, Filip, Collins, Amanda, Bai, Ren-Yuan, Staedtke, Verena, Rusk, Anthony W., Tung, David, Miller, Maria, Roix, Jeffrey, Khanna, Kristen V., Murthy, Ravi, Benjamin, Robert S., Helgason, Thorunn, Szvalb, Ariel D., Bird, Justin E., Roy-Chowdhuri, Sinchita, Zhang, Halle H., Qiao, Yuan, Karim, Baktiar, McDaniel, Jennifer, Elpiner, Amanda, Sahora, Alexandra, Lachowicz, Joshua, Phillips, Brenda, Turner, Avenelle, Klein, Mary K., Post, Gerald, Diaz, Luis A., Riggins, Gregory J., Papadopoulos, Nickolas, Kinzler, Kenneth W., Vogelstein, Bert, Bettegowda, Chetan, Huso, David L., Varterasian, Mary, Saha, Saurabh, Zhou, Shibin
Argitaratua izan da Sci Transl Med (2014)

How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

nork Banka, Siddharth, Veeramachaneni, Ratna, Reardon, William, Howard, Emma, Bunstone, Sancha, Ragge, Nicola, Parker, Michael J, Crow, Yanick J, Kerr, Bronwyn, Kingston, Helen, Metcalfe, Kay, Chandler, Kate, Magee, Alex, Stewart, Fiona, McConnell, Vivienne P M, Donnelly, Deirdre E, Berland, Siren, Houge, Gunnar, Morton, Jenny E, Oley, Christine, Revencu, Nicole, Park, Soo-Mi, Davies, Sally J, Fry, Andrew E, Lynch, Sally Ann, Gill, Harinder, Schweiger, Susann, Lam, Wayne W K, Tolmie, John, Mohammed, Shehla N, Hobson, Emma, Smith, Audrey, Blyth, Moira, Bennett, Christopher, Vasudevan, Pradeep C, García-Miñaúr, Sixto, Henderson, Alex, Goodship, Judith, Wright, Michael J, Fisher, Richard, Gibbons, Richard, Price, Susan M, C de Silva, Deepthi, Temple, I Karen, Collins, Amanda L, Lachlan, Katherine, Elmslie, Frances, McEntagart, Meriel, Castle, Bruce, Clayton-Smith, Jill, Black, Graeme C, Donnai, Dian
Argitaratua 2012

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

nork Mefford, Heather C., Sharp, Andrew J., Baker, Carl, Itsara, Andy, Jiang, Zhaoshi, Buysse, Karen, Huang, Shuwen, Maloney, Viv K., Crolla, John A., Baralle, Diana, Collins, Amanda, Mercer, Catherine, Norga, Koen, de Ravel, Thomy, Devriendt, Koen, Bongers, Ernie M.H.F., de Leeuw, Nicole, Reardon, William, Gimelli, Stefania, Bena, Frederique, Hennekam, Raoul C., Male, Alison, Gaunt, Lorraine, Clayton-Smith, Jill, Simonic, Ingrid, Park, Soo Mi, Mehta, Sarju G., Nik-Zainal, Serena, Woods, C. Geoffrey, Firth, Helen V., Parkin, Georgina, Fichera, Marco, Reitano, Santina, Giudice, Mariangela Lo, Li, Kelly E., Casuga, Iris, Broomer, Adam, Conrad, Bernard, Schwerzmann, Markus, Räber, Lorenz, Gallati, Sabina, Striano, Pasquale, Coppola, Antonietta, Tolmie, John L., Tobias, Edward S., Lilley, Chris, Armengol, Lluis, Spysschaert, Yves, Verloo, Patrick, De Coene, Anja, Goossens, Linde, Mortier, Geert, Speleman, Frank, van Binsbergen, Ellen, Nelen, Marcel R., Hochstenbach, Ron, Poot, Martin, Gallagher, Louise, Gill, Michael, McClellan, Jon, King, Mary-Claire, Regan, Regina, Skinner, Cindy, Stevenson, Roger E., Antonarakis, Stylianos E., Chen, Caifu, Estivill, Xavier, Menten, Björn, Gimelli, Giorgio, Gribble, Susan, Schwartz, Stuart, Sutcliffe, James S., Walsh, Tom, Knight, Samantha J.L., Sebat, Jonathan, Romano, Corrado, Schwartz, Charles E., Veltman, Joris A., de Vries, Bert B.A., Vermeesch, Joris R., Barber, John C.K., Willatt, Lionel, Tassabehji, May, Eichler, Evan E.
Argitaratua 2008