Geographic range size and speciation in honeyeaters von Hay, Eleanor M, McGee, Matthew D, Chown, Steven L

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Macroevolutionary dynamics of parasite diversification: A reality check von Hay, Eleanor M., Poulin, Robert, Jorge, Fátima

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Adequate sample sizes for improved accuracy of thermal trait estimates von Duffy, Grant A., Kuyucu, Arda C., Hoskins, Jessica L., Hay, Eleanor M., Chown, Steven L.

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Additional file 2 of Geographic range size and speciation in honeyeaters von Hay, Eleanor M., McGee, Matthew D., Chown, Steven L.

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Association of Neonatal Hypoglycemia With Academic Performance in Mid-Childhood von Shah, Rajesh, Dai, Darren W T, Alsweiler, Jane M, Brown, Gavin T L, Chase, J Geoffrey, Gamble, Gregory D, Harris, Deborah L, Keegan, Peter, Nivins, Samson, Wouldes, Trecia A, Thompson, Benjamin, Turuwhenua, Jason, Harding, Jane E, McKinlay, Christopher J D

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Diagnostic Delay in Pediatric Inflammatory Bowel Disease: A Systematic Review von Ajbar, Aymane, Cross, Eleanor, Matoi, Simbarashe, Hay, Charles A., Baines, Libby M., Saunders, Benjamin, Farmer, Adam D., Prior, James A.

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Effect of a Perioperative, Cardiac Output–Guided Hemodynamic Therapy Algorithm on Outcomes Following Major Gastrointestinal Surgery: A Randomized Clinical Trial and Systematic Revi... von Pearse, Rupert M, Harrison, David A, MacDonald, Neil, Gillies, Michael A, Blunt, Mark, Ackland, Gareth, Grocott, Michael P. W, Ahern, Aoife, Griggs, Kathryn, Scott, Rachael, Hinds, Charles, Rowan, Kathryn

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Microbial genomics amidst the Arctic crisis von Edwards, Arwyn, Cameron, Karen A, Cook, Joseph M, Debbonaire, Aliyah R, Furness, Eleanor, Hay, Melanie C, Rassner, Sara M E

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Ecological gradients drive insect wing loss and speciation: The role of the alpine treeline von McCulloch, Graham A., Foster, Brodie J., Dutoit, Ludovic, Ingram, Travis, Hay, Eleanor, Veale, Andrew J., Dearden, Peter K., Waters, Jonathan M.

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The Phenotypic Continuum of ATP1A3 -Related Disorders von Vezyroglou, Aikaterini, Akilapa, Rhoda, Barwick, Katy, Koene, Saskia, Brownstein, Catherine A., Holder-Espinasse, Muriel, Fry, Andrew E., Németh, Andrea H., Tofaris, George K., Hay, Eleanor, Hughes, Imelda, Mansour, Sahar, Mordekar, Santosh R., Splitt, Miranda, Turnpenny, Peter D., Demetriou, Demetria, Koopmann, Tamara T., Ruivenkamp, Claudia A.L., Agrawal, Pankaj B., Carr, Lucinda, Clowes, Virginia, Ghali, Neeti, Holder, Susan Elizabeth, Radley, Jessica, Male, Alison, Sisodiya, Sanjay M., Kurian, Manju A., Cross, J. Helen, Balasubramanian, Meena

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PLAC8-Mediated Activation of NOX4 Signalling Restores Angiogenic Function of Endothelial Colony-Forming Cells in Experimental Hypoxia von Pun, Shun Hay, O'Neill, Karla M, Edgar, Kevin S, Gill, Eleanor K, Moez, Arya, Naderi-Meshkin, Hojjat, Malla, Sudhir B, Hookham, Michelle B, Alsaggaf, Mohammed, Madishetti, Vinuthna Vani, Botezatu, Bianca, King, William, Brunssen, Coy, Morawietz, Henning, Dunne, Philip D, Brazil, Derek P, Medina, Reinhold J, Watson, Chris J, Grieve, David J

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Parasitological research in the molecular age von Selbach, Christian, Jorge, Fátima, Dowle, Eddy, Bennett, Jerusha, Chai, Xuhong, Doherty, Jean-François, Eriksson, Alan, Filion, Antoine, Hay, Eleanor, Herbison, Ryan, Lindner, Jocelyn, Park, Eunji, Presswell, Bronwen, Ruehle, Brandon, Sobrinho, Paulo M., Wainwright, Eleanor, Poulin, Robert

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Clinical spectrum of ectopia lentis presenting to a specialist children’s hospital von Williams, Katie M., Das, Aditi, Gomez, Belen, Cullop, Thomas, Hay, Eleanor, Lloyd, I. Christopher

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Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation von Bernkopf, Marie, Abdullah, Ummi B., Bush, Stephen J., Wood, Katherine A., Ghaffari, Sahar, Giannoulatou, Eleni, Koelling, Nils, Maher, Geoffrey J., Thibaut, Loïc M., Williams, Jonathan, Blair, Edward M., Kelly, Fiona Blanco, Bloss, Angela, Burkitt-Wright, Emma, Canham, Natalie, Deng, Alexander T., Dixit, Abhijit, Eason, Jacqueline, Elmslie, Frances, Gardham, Alice, Hay, Eleanor, Holder, Muriel, Homfray, Tessa, Hurst, Jane A., Johnson, Diana, Jones, Wendy D., Kini, Usha, Kivuva, Emma, Kumar, Ajith, Lees, Melissa M., Leitch, Harry G., Morton, Jenny E. V., Németh, Andrea H., Ramachandrappa, Shwetha, Saunders, Katherine, Shears, Deborah J., Side, Lucy, Splitt, Miranda, Stewart, Alison, Stewart, Helen, Suri, Mohnish, Clouston, Penny, Davies, Robert W., Wilkie, Andrew O. M., Goriely, Anne

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Mortality due to falls by county, age group, race, and ethnicity in the USA, 2000–19: a systematic analysis of health disparities von Kendrick, Parkes, Kelly, Yekaterina O, Baumann, Mathew M, Kahn, Ethan, Compton, Kelly, Schmidt, Chris, Sylte, Dillon O, Li, Zhuochen, La Motte-Kerr, Wichada, Daoud, Farah, Ong, Kanyin Liane, Moberg, Madeline, Hay, Simon I, Rodriquez, Erik J, Strassle, Paula D, Mensah, George A, Bandiera, Frank C, George, Stephanie M, Simonsick, Eleanor M, Brown, Colleen, Pérez-Stable, Eliseo J, Murray, Christopher J L, Mokdad, Ali H, Dwyer-Lindgren, Laura

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Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships—allelic requirement, inheritance modes, and d... von Roberts, Angharad M., DiStefano, Marina T., Riggs, Erin Rooney, Josephs, Katherine S., Alkuraya, Fowzan S., Amberger, Joanna, Amin, Mutaz, Berg, Jonathan S., Cunningham, Fiona, Eilbeck, Karen, Firth, Helen V., Foreman, Julia, Hamosh, Ada, Hay, Eleanor, Leigh, Sarah, Martin, Christa L., McDonagh, Ellen M., Perrett, Daniel, Ramos, Erin M., Robinson, Peter N., Rath, Ana, Sant, David W., Stark, Zornitza, Whiffin, Nicola, Rehm, Heidi L., Ware, James S.

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De novo variants in KCNA3 cause developmental and epileptic encephalopathy von Soldovieri, Maria Virginia, Ambrosino, Paolo, Mosca, Ilaria, Servettini, Ilenio, Pietrunti, Francesca, Belperio, Giorgio, Syrbe, Steffen, Taglialatela, Maurizio, Lemke, Johannes R

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The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders von Sidpra, Jai, Sudhakar, Sniya, Biswas, Asthik, Massey, Flavia, Turchetti, Valentina, Lau, Tracy, Cook, Edward, Alvi, Javeria Raza, Elbendary, Hasnaa M, Jewell, Jerry L, Riva, Antonella, Orsini, Alessandro, Vignoli, Aglaia, Federico, Zara, Rosenblum, Jessica, Schoonjans, An-Sofie, de Wachter, Matthias, Delgado Alvarez, Ignacio, Felipe-Rucián, Ana, Haridy, Nourelhoda A, Haider, Shahzad, Zaman, Mashaya, Banu, Selina, Anwaar, Najwa, Rahman, Fatima, Maqbool, Shazia, Yadav, Rashmi, Salpietro, Vincenzo, Maroofian, Reza, Patel, Rajan, Radhakrishnan, Rupa, Prabhu, Sanjay P, Lichtenbelt, Klaske, Stewart, Helen, Murakami, Yoshiko, Löbel, Ulrike, D'Arco, Felice, Wakeling, Emma, Jones, Wendy, Hay, Eleanor, Bhate, Sanjay, Jacques, Thomas S, Mirsky, David M, Whitehead, Matthew T, Zaki, Maha S, Sultan, Tipu, Striano, Pasquale, Jansen, Anna C, Lequin, Maarten, de Vries, Linda S, Severino, Mariasavina, Edmondson, Andrew C, Menzies, Lara, Campeau, Philippe M, Houlden, Henry, McTague, Amy, Efthymiou, Stephanie, Mankad, Kshitij

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Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders von Jurgens, Julie A., Barry, Brenda J., Chan, Wai-Man, MacKinnon, Sarah, Matos Ruiz, Paola M., England, Eleina M., Pais, Lynn, Groopman, Emily, Russell, Kathryn A., Di Gioia, Silvio Alessandro, Lee, Arthur S., Shaaban, Sherin, Bekele, Sarah, Toffoloni, Melissa, Foster, Emma E., Berube, Lindsay, Rivera-Quiles, Cristina, Mensching, Fiona M., Sanchis-Juan, Alba, Fu, Jack M., Wong, Isaac, Zhao, Xuefang, Wilson, Michael W., Lek, Monkol, Abarca-Barriga, Hugo, Al-Haddad, Christiane, Chacon-Camacho, Oscar Francisco, Chang, Lan, Christiansen, Stephen P., Ciccarelli, Maria Laura, Cordonnier, Monique, Cox, Gerald F., Curry, Cynthia J., Lee Dahm, Thomas, David, Karen L., De Berardinis, Teresa, Demer, Joseph L., Drack, Arlene V., Eggenberger, Eric, Elder, James E., Elliott, Alexandra T., Epley, K. David, Feldman, Hagit Baris, Ferreira, Carlos R., Gerth-Kahlert, Christina, Halliday, Dorothy J., Hanisch, Frank, Hay, Eleanor, Holder, Christopher, Iannaccone, Alessandro, Isenberg, Sherwin J., Kahana, Alon, Kazlas, Melanie, Kerr, Natalie C., Ko, Melissa W., Koc, Feray, Larsen, Dorte Ancher, Lay-Son, Guillermo, Ledoux, Danielle M., Levin, Alex V., Levy, Richard L., Mackey, David A., Mantagos, Iason S., Marti, Candice, Menezes, Manoj P., Mikail, Claudia N., Miller, Kathryn Bisceglia, Miyana, Kaori, Mullineaux, Lisa, Nishimura, Julie K., Noble, A. Gwendolyn, Pavone, Piero, Phalen, James A., Poduri, Annapurna, Polo, Claudia R., Prasov, Lev, Ramos, Feliciano J., Ramos-Caceres, Maria, Robb, Richard M., Rossillion, Béatrice, Smith, Lois E.H., Sorkin, Jeffrey A., Soul, Janet S., Stalker, Heather J., Stasheff, Steven F., Strassberg, Sonya, Thomas, Ioan Talfryn, VanderVeen, Deborah K., Vincent, Andrea L., Wabbels, Bettina, Wong, Agnes M.F., Wu, Carolyn, Yeung, Alison, Young, Terri L., Zwaan, Johan, Brand, Harrison, Talkowski, Michael E., MacArthur, Daniel G., Robson, Caroline D., Engle, Elizabeth C.

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The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders von Sidpra, Jai, Sudhakar, Sniya, Biswas, Asthik, Massey, Flavia, Turchetti, Valentina, Lau, Tracy, Cook, Edward, Alvi, Javeria Raza, Elbendary, Hasnaa M, Jewell, Jerry L, Riva, Antonella, Orsini, Alessandro, Vignoli, Aglaia, Federico, Zara, Rosenblum, Jessica, Schoonjans, An-Sofie, de Wachter, Matthias, Delgado Alvarez, Ignacio, Felipe-Rucián, Ana, Haridy, Nourelhoda A, Haider, Shahzad, Zaman, Mashaya, Banu, Selina, Anwaar, Najwa, Rahman, Fatima, Maqbool, Shazia, Yadav, Rashmi, Salpietro, Vincenzo, Maroofian, Reza, Patel, Rajan, Radhakrishnan, Rupa, Prabhu, Sanjay P, Lichtenbelt, Klaske, Stewart, Helen, Murakami, Yoshiko, Löbel, Ulrike, D'Arco, Felice, Wakeling, Emma, Jones, Wendy, Hay, Eleanor, Bhate, Sanjay, Jacques, Thomas S, Mirsky, David M, Whitehead, Matthew T, Zaki, Maha S, Sultan, Tipu, Striano, Pasquale, Jansen, Anna C, Lequin, Maarten, de Vries, Linda S, Severino, Mariasavina, Edmondson, Andrew C, Menzies, Lara, Campeau, Philippe M, Houlden, Henry, McTague, Amy, Efthymiou, Stephanie, Mankad, Kshitij

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