C9orf72 Gene-Associated Frontotemporal Dementia Mimicking Autoimmune Pathology.

Hoshina Y, Moser C, Wright MA, Sunderman E, Livsey CT, Spoth E, Clardy SL, Cliatt Brown CJ

Comparison of highly sensitive, multiplex immunoassay platforms for streamlined clinical cytokine quantification.

McKinski K, Tang H, Wang K, Birchler M, Wright M

The Moderating Effect of Peer Attachment on Associations Between Children's and Adolescents' Cyberbullying Victimization, Bystanding, and Depressive Symptoms.

Wright MF

Does cognitive intra-individual variability predict change in everyday functioning performance in women with and without HIV in the Women's Interagency HIV Study?

Vance DE, Xu Y, Dastgheyb R, Maki PM, Zhang J, Springer G, Anastos K, Gustafson DR, Weber KM, Dykxhoorn DM, Milam J, Diaz MM, Kassaye SG, Waldrop D, Lee J, Kempf MC, Konkle-Parker D, Goodkin K, Leviner AJ, Wright M, Jones D, Rubin LH

The moderating effect of parental mediation in the longitudinal associations among cyberbullying, depression, and self-harm among Chinese and American adolescents.

Wright MF

The different serum albumin assays influence calcium status in haemodialysis patients: a comparative study against free calcium as a reference method.

Eisa O, Dafaalla M, Wright M, Faisal M, Stuart K, Jassam N

Discovery of NP3-253, a Potent Brain Penetrant Inhibitor of the NLRP3 Inflammasome.

Mackay A, Velcicky J, Gommermann N, Mattes H, Janser P, Wright M, Dubois C, Brenneisen S, Ilic S, Vangrevelinghe E, Stiefl N, Boettcher A, Schoenboerner M, Vogelsanger M, Muller-Bentz S, Kamke M, Rubert J, Kauffmann M, Desrayaud S, Trunzer M, Srinivas H, Hinniger A, von Burg N, Beltz K, Dekker C, Farady CJ

Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection.

Kingsmore SF, Wright M, Smith LD, Liang Y, Mowrey WR, Protopsaltis L, Bainbridge M, Baker M, Batalov S, Blincow E, Cao B, Caylor S, Chambers C, Ellsworth K, Feigenbaum A, Frise E, Guidugli L, Hall KP, Hansen C, Kiel M, Van Der Kraan L, Krilow C, Kwon H, Madhavrao L, Lefebvre S, Leipzig J, Mardach R, Moore B, Oh D, Olsen L, Ontiveros E, Owen MJ, Reimers R, Scharer G, Schleit J, Shelnutt S, Mehtalia SS, Oriol A, Sanford E, Schwartz S, Wigby K, Willis MJ, Yandell M, Kunard CM, Defay T

Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial.

Kingsmore SF, Wright M, Olsen L, Schultz B, Protopsaltis L, Averbuj D, Blincow E, Carroll J, Caylor S, Defay T, Ellsworth K, Feigenbaum A, Gover M, Guidugli L, Hansen C, Van Der Kraan L, Kunard CM, Kwon H, Madhavrao L, Leipzig J, Liang Y, Mardach R, Mowrey WR, Nguyen H, Niemi AK, Oh D, Saad M, Scharer G, Schleit J, Mehtalia SS, Sanford E, Smith LD, Willis MJ, Wigby K, Reimers R

The ALS-associated co-chaperone DNAJC7 mediates neuroprotection against proteotoxic stress by modulating HSF1 activity.

Fleming AC, Rao NR, Wright M, Savas JN, Kiskinis E

The menstrual phase does not impact chemosensitivity during exercise.

Mann LM, Wright MD, Thompson BP, Chang JC, Chan JS, Foster GE, Dominelli PB

Understanding general practice funding models in Australia and beyond.

Chen W, van Gool K, Wright M

Constrained TACC3 peptidomimetics for a non-canonical protein-protein interface elucidate allosteric communication in Aurora-A kinase.

Gimenez D, Walko M, Miles JA, Bayliss R, Wright MH, Wilson AJ

Rare disease genomic testing in the UK and Ireland: promoting timely and equitable access.

Ellard S, Morgan S, Wynn SL, Walker S, Parrish A, Mein R, Juett A, Ahn JW, Berry I, Cassidy EJ, Durkie M, Fish L, Hall R, Howard E, Rankin J, Wright CF, Deans ZC, Scott RH, Hill SL, Baple EL, Taylor RW, Association for Clinical Genomic Science Rare Disease Position Statement Working Group

Sniffing out morphological convergence in the turbinal complex of myrmecophagous placentals.

Wright M, Martinez Q, Ferreira-Cardoso S, Lebrun R, Dubourguier B, Delsuc F, Fabre PH, Hautier L