Current global status of male reproductive health

- De Jonge, Christopher K., Barratt, Christopher L. R., Kimmins, Sarah, Krausz, Csilla, McLachlan, Robert I., Niederberger, Craig, O'Bryan, Moira K., Pacey, Allan, Priskorn, Lærke, Rautakallio-Hokkanen, Satu, Serour, Gamal, Veltman, Joris A., Aitken, R. John, Vogel, DL, Vazquez-Levin, MH, Anderson, Richard A., Baker, Peter, Chan, David Y. L., Connolly, Mark P., Eisenberg, Michael L., Garrido, Nicolas, Jørgensen, Niels

Genetic variants for head size share genes and pathways with cancer

- Knol, Maria J., Poot, Raymond A., van Dam-Nolen, Dianne H. K., Brunner, HG, Le Grand, Q, Sim, K, Stein, DJ, Bowden, DW, Cairns, MJ, Hariri, AR, Cheung, C-L, Andersson, S, Villringer, A, Lamballais, Sander, Paus, T, Cichon, S, Calhoun, VD, Crivello, F, Launer, LJ, White, T, Koudstaal, PJ, Houlden, H, Fornage, M, Matsuda, F, Pawlak, Mikolaj A., Grabe, HJ, Ikram, MA, Debette, S, Thompson, PM, Seshadri, S, Adams, HHH, Lewis, Cora E., Carrion-Castillo, Amaia, van Erp, Theo G. M., Reinbold, Céline S., Shin, Jean, Scholz, Markus, Håberg, Asta K., Evans, Tavia E., Kämpe, Anders, Li, GHY, Avinun, R, Atkins, Joshua R., Hsu, F-C, Amod, AR, Lam, M, Tsuchida, A, Teunissen, MWA, Aygün, N, Satizabal, Claudia L., Patel, Y, Liang, D, Beiser, AS, Beyer, F, Bis, JC, Bos, D, Bryan, RN, Bülow, R, Caspers, S, Catheline, G, Mishra, Aniket, Cecil, CAM, Dalvie, S, Dartigues, J-F, DeCarli, C, Enlund-Cerullo, M, Ford, JM, Franke, B, Freedman, BI, Friedrich, N, Green, MJ, Sargurupremraj, Muralidharan, Haworth, S, Helmer, C, Hoffmann, P, Homuth, G, Ikram, MK, Jack, CR, Jahanshad, N, Jockwitz, C, Kamatani, Y, Knodt, AR, van der Auwera, Sandra, Li, S, Lim, K, Longstreth, WT, Macciardi, F, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium,, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium,, Mäkitie, O, Mazoyer, B, Medland, SE, Miyamoto, S, Duperron, Marie-Gabrielle, Moebus, S, Mosley, TH, Muetzel, R, Mühleisen, TW, Nagata, M, Nakahara, S, Palmer, ND, Pausova, Z, Preda, A, Quidé, Y, Jian, Xueqiu, Reay, WR, Roshchupkin, GV, Schmidt, R, Schreiner, PJ, Setoh, K, Shapland, CY, Sidney, S, St Pourcain, B, Stein, JL, Tabara, Y, Hostettler, Isabel C., Teumer, A, Uhlmann, A, van der Lugt, A, Vernooij, MW, Werring, DJ, Windham, BG, Witte, AV, Wittfeld, K, Yang, Q, Yoshida, K

No evidence for association between rs10191329 severity locus and longitudinal disease severity in 1813 relapse-onset multiple sclerosis patients from the MSBase registry

- Campagna, Maria Pia, Havrdova, Eva Kubala, van der Walt, Anneke, Butzkueven, Helmut, Jokubaitis, Vilija G., Horakova, Dana, Izquierdo, Guillermo, Matesanz, Fuencisla, Eichau, Sara, Lechner-Scott, Jeanette, Taylor, Bruce Multiple sclerosis, disease severity, genetics., Garcia-Sanchez, Maria-Isabel, Alcina, Antonio

Using Genetics to Inform Interventions Related to Sodium and Potassium in Hypertension

- Reay, William R., Clarke, Erin, Collins, Clare E., Cairns, Murray J., Eslick, Shaun, Riveros, Carlos, Holliday, Elizabeth G., McEvoy, Mark A., Peel, Roseanne, Hancock, Stephen, Scott, Rodney J., Attia, John R.

Changes in Refractive Error During Young Adulthood: The Effects of Longitudinal Screen Time, Ocular Sun Exposure, and Genetic Predisposition

- Lee, Samantha Sze-Yee, Lingham, Gareth, Wang, Carol A., Diaz Torres, Santiago, Pennell, Craig E., Hysi, Pirro G., Hammond, Christopher J., Gharahkhani, Puya, Clark, Rosie, Guggenheim, Jeremy A., Mackey, David A.

Employing SNP data to reveal population status and breeding secrets of two cryptic, endangered frog species

- Stock, Sarah

Exploring opportunities for drug repurposing and precision medicine in cannabis use disorder using genetics

- Greco, Laura A., Reay, William R., Dayas, Christopher V., Cairns, Murray J.

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

- Li, Josephine H., Brenner, Laura N., Corbin, Laura J., Luan, Jian'an, Willems, Sara M., Wu, Ying, Zhang, Xiaoshuai, Horikoshi, Momoko, Boutin, Thibaud S., Mägi, Reedik, Waage, Johannes, Li-Gao, Ruifang, Kaur, Varinderpal, Chan, Kei Hang Katie, Pennell, Craig E., .,, Figueroa, Katherine, Schroeder, Philip, Huerta-Chagoya, Alicia, Chen, Ji, Spracklen, Cassandra N., Marenne, Gaëlle, Varshney, Arushi

Human Genetics Society of Australasia Position Statement: Use of Polygenic Scores in Clinical Practice and Population Health

- Young, Mary-Anne, Yanes, Tatiane, James, Paul A., Steinberg, Julia, Cust, Anne E., Dunlop, Kate, Limb, Sharne, Newson, Ainsley J., Purvis, Rebecca, Thiyagarajan, Lavvina, Scott, Rodney J., Verma, Kunal

MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome

- Wiik, Mariann Unhjem, Negline, Mia, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A., Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan

Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity

- Jokubaitis, Vilija G., Campagna, Maria Pia, Lea, Rodney, Kilpatrick, Trevor J., Kalincik, Tomas, De Jager, Philip L., Beecham, Ashley, McCauley, Jacob L., Taylor, Bruce V., Vucic, Steve, Laverick, Louise, Vodehnalova, Karolina, Ibrahim, Omar, García-Sanchéz, Maria-Isabel, Alcina, A, van der Walt, A, Havrdova, EK, Izquierdo, G, Patsopoulos, N, Horakova, D, Butzkueven, H, Stankovich, Jim, Kleinova, Pavlina, Matesanz, Fuencisla, Hui, Daniel, Eichau, Sara, Slee, Mark, Lechner-Scott, Jeannette

Salt-taste polymorphism TRPV1-rs8065080 is associated with increased likelihood of depression in an elderly cohort

- Ferraris, Celeste, Scarlett, Christopher J., Veysey, Martin, Lucock, Mark, Bucher, Tamara, Beckett, Emma L.

The Effect of Genetic Predisposition to Alzheimer's Disease and Related Traits on Recruitment Bias in a Study of Cognitive Aging

- Gomez, Lina M., Mitchell, Brittany L., Lupton, Michelle K., McAloney, Kerrie, Adsett, Jessica, Garden, Natalie, Wood, Madeline, Diaz-Torres, Santiago, Garcia-Marin, Luis M., Breakspear, Michael, Martin, Nicholas G.

The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performance

- Brazane, Mira, Dimitrova, Dilyana G., Delatycki, Martin, Dudding-Byth, Tracy, Gecz, Jozef, Plaçais, Pierre-Yves, Teysset, Laure, Préat, Thomas, Piton, Amélie, Hassan, Bassem A., Roignant, Jean-Yves, Motorin, Yuri, Pigeon, Julien, Carré, Clément, Paolantoni, Chiara, Ye, Tao, Marchand, Virginie, Da Silva, Bruno, Schaefer, Elise, Angelova, Margarita T., Stark, Zornitza

Uncovering inbreeding, small populations, and strong genetic isolation in an Australian threatened frog, Litoria littlejohni

- Stock, Sarah E., Klop-Toker, Kaya, Wallace, Samantha, Kelly, Oliver, Callen, Alex, Seeto, Rebecca, Mahony, Stephen V., Hayward, Matt W., Mahony, Michael J.

Alterations in the p53 isoform ratio govern breast cancer cell fate in response to DNA damage

- Steffans Reinhardt, Luiza, Zhang, Xiajie, Groen, Kira, Morten, Brianna C., De Iuliis, Geoffry N., Braithwaite, Antony W., Bourdon, Jean-Christophe, Avery-Kiejda, Kelly A.

Cell type-specific manifestations of cortical thickness heterogeneity in schizophrenia

- Di Biase, Maria A., Geaghan, Michael P., Bouix, Sylvain, Knyazhanskaya, Evdokiya E., Lyall, Amanda E., Pasternak, Ofer, Kubicki, Marek, Rathi, Yogesh, Visco, Andrew, Gaunnac, Megan, Lv, Jinglei, Mesholam-Gately, Raquelle I., Reay, William R., Cairns, Murray J., Holt, DJ, Keshavan, MS, Pantelis, C, Öngür, D, Breier, A, Cairns, MJ, Shenton, ME, Zalesky, A, Seidlitz, Jakob, Weickert, Cynthia Shannon, Pébay, Alice, Green, Melissa J., Quidé, Yann, Atkins, Joshua R., Coleman, Michael J.

General intelligence and executive functioning are overlapping but separable at genetic and molecular pathway levels: An analytical review of existing GWAS findings

- Ciobanu, Liliana G., Stankov, Lazar, Schubert, K. Oliver, Amare, Azmeraw T., Jawahar, M. Catharine, Lawrence-Wood, Ellie, Mills, Natalie T., Knight, Matthew, Clark, Scott R., Aidman, Eugene

Genetic Basis of Childhood Cardiomyopathy

- Bagnall, Richard D., Singer, Emma S., Semsarian, Christopher, Wacker, Julie, Nowak, Natalie, Ingles, Jodie, King, Ingrid, Macciocca, Ivan, Crowe, Joshua, Ronan, Anne, Weintraub, Robert G.

Genetics-informed precision treatment formulation in schizophrenia and bipolar disorder

- Reay, William R., Geaghan, Michael P., Atkins, Joshua R., Carr, Vaughan J., Green, Melissa J., Cairns, Murray J.