A functional polymorphism in the interleukin-1beta and severity of nicotine dependence in male schizophrenia: a case-control study

- Zhang, Xiang Yang, Chen, Da-Chun, Correll, Christopher U., Wu, Jingqin, Soares, Jair C., Tan, Yun-Long, Tan, Shu-ping, Luo, Xingguang, Zuo, Lingjun, Rao, Wenwang, Yu, Qiong, Kou, Changgui, Allen, Melissa

Clinical perspectives on hereditary hemochromatosis

- Ayonrinde, Oyekoya T., Milward, Elizabeth A., Chua, Anita C. G., Trinder, Debbie, Olynyk, John K.

Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis

- Cox, Mathew B., Bowden, Nikola A., Scott, Rodney J., Lechner-Scott, Jeannette

Effect modification by transferrin C2 polymorphism on lead exposure, hemoglobin levels, and IQ

- Roy, Ananya, Ettinger, Adrienne S., Hu, Howard, Bellinger, David, Schwartz, Joel, Modali, Rama, Wright, Robert O., Palaniappan, Kavitha, Balakrishnan, Kalpana

Emergence of endemic MLST non-typeable vancomycin-resistant Enterococcus faecium

- Carter, Glen P., Buultjens, Andrew H., Howden, Benjamin P., Ballard, Susan A., Baines, Sarah L., Tomita, Takehiro, Strachan, Janet, Johnson, Paul D. R., Ferguson, John K., Seemann, Torsten, Stinear, Timothy P.

Immune checkpoint blockade in solid organ tumours: choice, dose and predictors of response

- Navani, Vishal, Graves, Moira C., Bowden, Nikola A., Van Der Westhuizen, Andre

Interleukin-6 gene promoter-572 C allele may play a role in rate of disease progression in multiple sclerosis

- Yan, Jun, Liu, Jia, Mason, Deborah, Griffiths, Lyn, Moscato, Pablo, Slee, Mark, Taylor, Bruce, Wiley, James, Field, Judith, Butzkueven, Helmut, Kilpatrick, Trevor J., Csurhes, Peter A., Lin, Clement Yihao, Pender, Michael P., McCombe, Pamela A., Greer, Judith M., Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZGene),, Scott, Rodney J., Lechner-Scott, Jeannette, Brown, Matthew A., Booth, David R., Stewart, Graeme J., Broadley, Simon

Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations

- Kairupan, Carla F., Meldrum, C. J., Crooks, R., Milward, E. A., Spigelman, Allan David, Burgess, B., Groombridge, C., Kirk, J., Tucker, K., Ward, R., Williams, R., Scott, Rodney J

Polymorphisms of 5-HTT LPR and GNβ3 825C>T and response to antidepressant treatment in functional dyspepsia: a study from the functional dyspepsia treatment trial

- Saito, Yuri A., Locke, G. Richard, Moayyedi, Paul, Herrick, Linda M., Szarka, Lawrence A., Camilleri, Michael, Hamilton, Frank A., Schleck, Cathy D., Tilkes, Katherine E., Zinsmeister, Alan R., Talley, Nicholas J., Almazar, Ann E., Bouras, Ernest P., Howden, Colin W., Lacy, Brian E., Dibaise, John K., Prather, Charlene M., Abraham, Bincy P., El-Serag, Hashem B.

Relationships between selected sweet and bitter-taste receptors and features of oral health

- Kaur, Kiranjit

Serotonin toxicity from antidepressant overdose and its association with the T102C polymorphism of the 5-HT₂A receptor

- Cooper, J. M., Newby, D. A., Whyte, I. M., Carter, G., Jones, A. L., Isbister, G. K.

Systematic review of genetic risk factors for sustaining a mild traumatic brain injury

- Panenka, William J., Gardner, Andrew J., Dretsch, Michael N., Crynen, Gogce C., Crawford, Fiona C., Iverson, Grant L.

TCF4 gene polymorphism is associated with cognition in patients with schizophrenia and healthy controls

- Hui, Li, Rao, Wen-Wang, Ruan, Li Na, Liu, Hong Yang, Hu, Wei Ming, Shao, Tian Nan, AngRabanes, Michael B., Soares, Jair C., Zhang, Xiang Yang, Yu, Qiong, Kou, Changgui, Wu, Jing Qin, He, Jin Cai, Ye, Min Jie, Liu, Jia Hong, Xu, Xiao Jun, Zheng, Ke

The influence of the Cyclin D1 870 G>A polymorphism as an endometrial cancer risk factor

- Ashton, Katie A., Proietto, Anthony, Otton, Geoffrey, Symonds, Ian, McEvoy, Mark, Attia, John, Gilbert, Michael, Hamann, Ute, Scott, Rodney J.

Towards Genotype-Specific Care for Chronic Hepatitis B: The First 6 Years Follow Up From the CHARM Cohort Study

- Davies, Jane, Smith, Emma L., Davis, Joshua S., Tong, Steven Y. C., Littlejohn, Margaret, Edwards, Rosalind, Sozzi, Vitina, Jackson, Kathy, McGuire, Katie, Binks, Paula, Cowie, Benjamin C., Locarnini, Stephen

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

- Davies, Robert W., Fiksinski, Ania M., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E., Breetvelt, Elemi J., Cubells, Joseph F., Eliez, Stephan, Garcia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan G., Philip, Nicole, Repetto, Gabriela M., Williams, Nigel M., Shashi, Vandana, Simon, Tony J., Suñer, Damiàn Heine, Vicari, Stefano, Scherer, Stephen W., Epstein, Michael P., Warren, Stephen T., Morrison, Sinead, Chawner, Samuel, Vingerhoets, Claudia, Hooper, Stephen R., Breckpot, Jeroen, Vergaelen, Elfi, Vogels, Annick, Monks, Stephen, Prasad, Sarah E., Sandini, Corrado, Schneider, Maude, Maeder, Johanna, Fraguas, David, Evers, Rens, Monfeuga, Thomas, Tassone, Flora, Morey-Canyelles, Jaume, Ousley, Opal Y., Antshel, Kevin M., Fremont, Wanda, Fritsch, Rosemarie, Ornstein, Claudia, Daly, Eileen M., Costain, Gregory A., Boot, Erik, Bassett, Anne S., Heung, Tracy, Crowley, T. Blaine, Zackai, Elaine H., Calkins, Monica E., Gur, Ruben C., McCabe, Kathryn L., Busa, Tiffany, Schoch, Kelly, Pontillo, Maria, Duijff, Sasja N., Owen, Michael J., Kahn, René S., Houben, Michiel, Kushan, Leila, Jalbrzikowski, Maria, Carmel, Miri, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Bearden, Carrie E., Vorstman, Jacob A. S., Gur, Raquel E., Morrow, Bernice E.