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Genomic variations associated with risk and protection against vincristine-induced peripheral neuropathy in pediatric cancer patients.
Published in:
NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00443-7
By:
- Mufti, Kheireddin;
- Cordova, Miguel;
- Scott, Erika N.;
- Trueman, Jessica N.;
- Lovnicki, Jessica M.;
- Loucks, Catrina M.;
- Rassekh, Shahrad R.;
- Ross, Colin J. D.;
- Carleton, Bruce C.;
- Groeneweg, Gabriella S. S.;
- Higginson, Michelle;
- Chang, Wan-Chun;
- Li, Kathy;
- Miao, Fudan;
- Yau, Derek;
- Pecheux, Lucie;
- Gyawali, Bina;
- Perreault, Amanda;
- Abbasi, Fatema;
- Guilcher, Gregory
Publication type:
Article
A Systematic Review of Polygenic Models for Predicting Drug Outcomes.
Published in:
Journal of Personalized Medicine, 2022, v. 12, n. 9, p. N.PAG, doi. 10.3390/jpm12091394
By:
- Siemens, Angela;
- Anderson, Spencer J.;
- Rassekh, S. Rod;
- Ross, Colin J. D.;
- Carleton, Bruce C.
Publication type:
Article
Improvement of Self-Injury With Dopamine and Serotonin Replacement Therapy in a Patient With a Hemizygous PAK3 Mutation: A New Therapeutic Strategy for Neuropsychiatric Features of an Intellectual Disability Syndrome.
Published in:
Journal of Child Neurology, 2018, v. 33, n. 1, p. 106, doi. 10.1177/0883073817740443
By:
- Horvath, Gabriella A.;
- Tarailo-Graovac, Maja;
- Bartel, Tanja;
- Race, Simone;
- Van Allen, Margot I.;
- Blydt-Hansen, Ingrid;
- Ross, Colin J.;
- Wasserman, Wyeth W.;
- Connolly, Mary B.;
- van Karnebeek, Clara D. M.
Publication type:
Article
Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease.
Published in:
2017
By:
- Tarailo-Graovac, Maja;
- Drögemöller, Britt I.;
- Wasserman, Wyeth W.;
- Ross, Colin J. D.;
- van den Ouweland, Ans M. W.;
- Darin, Niklas;
- Kollberg, Gittan;
- van Karnebeek, Clara D. M.;
- Blomqvist, Maria
Publication type:
journal article
Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms.
Published in:
Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0248-3
By:
- Sirrs, Sandra;
- van Karnebeek, Clara DM;
- Peng, Xiaoxue;
- Shyr, Casper;
- Tarailo-Graovac, Maja;
- Mandal, Rupasri;
- Testa, Daniel;
- Dubin, Devin;
- Carbonetti, Gregory;
- Glynn, Steven E.;
- Sayson, Bryan;
- Robinson, Wendy P.;
- Han, Beomsoo;
- Wishart, David;
- Ross, Colin J.;
- Wasserman, Wyeth W.;
- Hurwitz, Trevor A.;
- Sinclair, Graham;
- Kaczocha, Martin
Publication type:
Article
The genotypic and phenotypic spectrum of PIGA deficiency.
Published in:
Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0243-8
By:
- Tarailo-Graovac, Maja;
- Sinclair, Graham;
- Stockler-Ipsiroglu, Sylvia;
- Van Allen, Margot;
- Rozmus, Jacob;
- Shyr, Casper;
- Biancheri, Roberta;
- Tracey Oh;
- Sayson, Bryan;
- Lafek, Mirafe;
- Ross, Colin J.;
- Robinson, Wendy P.;
- Wasserman, Wyeth W.;
- Rossi, Andrea;
- van Karnebeek, Clara D. M.
Publication type:
Article
Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms.
Published in:
2015
By:
- Sirrs, Sandra;
- van Karnebeek, Clara Dm;
- Peng, Xiaoxue;
- Shyr, Casper;
- Tarailo-Graovac, Maja;
- Mandal, Rupasri;
- Testa, Daniel;
- Dubin, Devin;
- Carbonetti, Gregory;
- Glynn, Steven E;
- Sayson, Bryan;
- Robinson, Wendy P;
- Han, Beomsoo;
- Wishart, David;
- Ross, Colin J;
- Wasserman, Wyeth W;
- Hurwitz, Trevor A;
- Sinclair, Graham;
- Kaczocha, Martin;
- van Karnebeek, Clara D M
Publication type:
journal article
Single Point Mutation in Rabenosyn-5 in a Female with Intractable Seizures and Evidence of Defective Endocytotic Trafficking.
Published in:
2014
By:
- Stockler, Sylvia;
- Corvera, Silvia;
- Lambright, David;
- Fogarty, Kevin;
- Nosova, Ekaterina;
- Leonard, Deborah;
- Steinfeld, Robert;
- Ackerley, Cameron;
- Shyr, Casper;
- Au, Nicolas;
- Selby, Kathrin;
- Van Allen, Margot;
- Vallance, Hilary;
- Wevers, Ron;
- Watkins, David;
- Rosenblatt, David;
- Ross, Colin J.;
- Conibear, Elizabeth;
- Wasserman, Wyeth;
- Karnebeek, Clara van
Publication type:
Case Study
Single point mutation in Rabenosyn-5 in a female with intractable seizures and evidence of defective endocytotic trafficking.
Published in:
2014
By:
- Stockler, Sylvia;
- Corvera, Silvia;
- Lambright, David;
- Fogarty, Kevin;
- Nosova, Ekaterina;
- Leonard, Deborah;
- Steinfeld, Robert;
- Ackerley, Cameron;
- Shyr, Casper;
- Au, Nicolas;
- Selby, Kathrin;
- van Allen, Margot;
- Vallance, Hilary;
- Wevers, Ron;
- Watkins, David;
- Rosenblatt, David;
- Ross, Colin J;
- Conibear, Elizabeth;
- Wasserman, Wyeth;
- van Karnebeek, Clara
Publication type:
journal article
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome.
Published in:
Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-15
By:
- Demos, Michelle K.;
- van Karnebeek, Clara D. M.;
- Ross, Colin J. D.;
- Adam, Shelin;
- Yaoqing Shen;
- Shing Hei Zhan;
- Shyr, Casper;
- Horvath, Gabriella;
- Mohnish Suri;
- Fryer, Alan;
- Jones, Steven J. M.;
- Friedman, Jan M.
Publication type:
Article
Development of a cost-efficient novel method for rapid, concurrent genotyping of five common single nucleotide polymorphisms of the brain derived neurotrophic factor (BDNF) gene by tetra-primer amplification refractory mutation system.
Published in:
International Journal of Methods in Psychiatric Research, 2015, v. 24, n. 3, p. 235, doi. 10.1002/mpr.1475
By:
- Wang, Cathy K.;
- Xu, Michael S.;
- Ross, Colin J.;
- Lo, Ryan;
- Procyshyn, Ric M.;
- Vila‐Rodriguez, Fidel;
- White, Randall F.;
- Honer, William G.;
- Barr, Alasdair M.
Publication type:
Article
CYP2D6 as a treatment decision aid for ER-positive non-metastatic breast cancer patients: a systematic review with accompanying clinical practice guidelines.
Published in:
Breast Cancer Research & Treatment, 2019, v. 173, n. 3, p. 521, doi. 10.1007/s10549-018-5027-0
By:
- Drögemöller, Britt I.;
- Wright, Galen E. B.;
- Shih, Joanne;
- Monzon, Jose G.;
- Gelmon, Karen A.;
- Ross, Colin J. D.;
- Amstutz, Ursula;
- Carleton, Bruce C.;
- the CPNDS Clinical Recommendations Group
Publication type:
Article
Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy.
Published in:
Child Neurology Open, 2016, v. 3, p. 1, doi. 10.1177/2329048X16669912
By:
- Lee, Jessica J. Y.;
- van Karnebeek, Clara D. M.;
- Drögemoller, Britt;
- Shyr, Casper;
- Tarailo-Graovac, Maja;
- Eydoux, Patrice;
- Ross, Colin J.;
- Wasserman, Wyeth W.;
- Björnson, Bruce;
- Wu, John K.
Publication type:
Article
Design and Methods of the Pan-Canadian Applying Biomarkers to Minimize Long-Term Effects of Childhood/Adolescent Cancer Treatment (ABLE) Nephrotoxicity Study: A Prospective Observational Cohort Study.
Published in:
Canadian Journal of Kidney Health & Disease, 2017, p. 1, doi. 10.1177/2054358117690338
By:
- McMahon, Kelly R.;
- Rassekh, Shahrad Rod;
- Schultz, Kirk R.;
- Pinsk, Maury;
- Blydt-Hansen, Tom;
- Mammen, Cherry;
- Tsuyuki, Ross T.;
- Devarajan, Prasad;
- Cuvelier, Geoff D. E.;
- Mitchell, Lesley G.;
- Baruchel, Sylvain;
- Palijan, Ana;
- Carleton, Bruce C.;
- Ross, Colin J. D.;
- Zappitelli, Michael
Publication type:
Article
A systematic review of the effects of CYP2D6 phenotypes on risperidone treatment in children and adolescents.
Published in:
Child & Adolescent Psychiatry & Mental Health, 2018, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13034-018-0243-2
By:
- Dodsworth, Thomas;
- Kim, David D.;
- Procyshyn, Ric M.;
- Ross, Colin J.;
- Honer, William G.;
- Barr, Alasdair M.
Publication type:
Article
A girl with developmental delay, ataxia, cranial nerve palsies, severe respiratory problems in infancy-Expanding NDST1 syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 3, p. 712, doi. 10.1002/ajmg.a.37621
By:
- Armstrong, Linlea;
- Tarailo‐Graovac, Maja;
- Sinclair, Graham;
- Seath, Kimberly I.;
- Wasserman, Wyeth W.;
- Ross, Colin J.;
- van Karnebeek, Clara D. M.
Publication type:
Article
A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer.
Published in:
Nature Genetics, 2015, v. 47, n. 9, p. 1079, doi. 10.1038/ng.3374
By:
- Rassekh, Shahrad R;
- Rieder, Michael J;
- Visscher, Henk;
- Brunham, Liam R;
- Lee, Jong W;
- Carleton, Bruce C;
- van Dalen, Elvira C;
- Aminkeng, Folefac;
- Amstutz, Ursula;
- Caron, Huib N;
- Li, Yuling;
- Hayden, Michael R;
- Bernstein, Daniel;
- Bhavsar, Amit P;
- Kremer, Leontien C;
- van der Pal, Helena J;
- Ross, Colin J D
Publication type:
Article
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.
Published in:
Nature Genetics, 2013, v. 45, n. 5, p. 578, doi. 10.1038/ng.0513-578
By:
- Ross, Colin J D;
- Katzov-Eckert, Hagit;
- Dubé, Marie-Pierre;
- Brooks, Beth;
- Rassekh, S Rod;
- Barhdadi, Amina;
- Feroz-Zada, Yassamin;
- Visscher, Henk;
- Brown, Andrew M K;
- Rieder, Michael J;
- Rogers, Paul C;
- Phillips, Michael S;
- Carleton, Bruce C;
- Hayden, Michael R
Publication type:
Article
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.
Published in:
Nature Genetics, 2009, v. 41, n. 12, p. 1345, doi. 10.1038/ng.478
By:
- Ross, Colin J. D.;
- Katzov-Eckert, Hagit;
- Dubé, Marie-Pierre;
- Brooks, Beth;
- Rassekh, S. Rod;
- Barhdadi, Amina;
- Feroz-Zada, Yassamin;
- Visscher, Henk;
- Brown, Andrew M. K.;
- Rieder, Michael J.;
- Rogers, Paul C.;
- Phillips, Michael S.;
- Carleton, Bruce C.;
- Hayden, Michael R.
Publication type:
Article
Amelioration of Hypertriglyceridemia with Hypo-Alpha- Cholesterolemia in LPL Deficient Mice by Hematopoietic Cell-Derived LPL.
Published in:
PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0025620
By:
- Ding, Yinyuan;
- Zhang, Ling;
- Wang, Yuhui;
- Huang, Wei;
- Tang, Yin;
- Bai, Lu;
- Ross, Colin J. D.;
- Hayden, Michael R.;
- Liu, George
Publication type:
Article
Transcriptome-wide association study uncovers the role of essential genes in anthracycline-induced cardiotoxicity.
Published in:
NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00199-4
By:
- Scott, Erika N.;
- Wright, Galen E. B.;
- Drögemöller, Britt I.;
- Hasbullah, Jafar S.;
- Gunaretnam, Erandika P.;
- Miao, Fudan;
- Bhavsar, Amit P.;
- Shen, Fei;
- Schneider, Bryan P.;
- Carleton, Bruce C.;
- Ross, Colin J. D.
Publication type:
Article
Use of pharmacogenomics in pediatric renal transplant recipients.
Published in:
Frontiers in Genetics, 2015, v. 6, p. 1, doi. 10.3389/fgene.2015.00041
By:
- Medeiros, Mara;
- Castañeda-Hernández, Gilberto;
- Ross, Colin J. D.;
- Carleton, Bruce C.
Publication type:
Article
Pharmacogenomic screening for anthracycline-induced cardiotoxicity in childhood cancer.
Published in:
British Journal of Clinical Pharmacology, 2017, v. 83, n. 5, p. 1143, doi. 10.1111/bcp.13218
By:
- Aminkeng, Folefac;
- Ross, Colin J. D.;
- Rassekh, Shahrad R.;
- Rieder, Michael J.;
- Bhavsar, Amit P.;
- Sanatani, Shubhayan;
- Bernstein, Daniel;
- Hayden, Michael R.;
- Amstutz, Ursula;
- Carleton, Bruce C.
Publication type:
Article
Recommendations for genetic testing to reduce the incidence of anthracycline-induced cardiotoxicity.
Published in:
British Journal of Clinical Pharmacology, 2016, v. 82, n. 3, p. 683, doi. 10.1111/bcp.13008
By:
- Aminkeng, Folefac;
- Ross, Colin J. D.;
- Rassekh, Shahrad R.;
- Hwang, Soomi;
- Rieder, Michael J.;
- Bhavsar, Amit P.;
- Smith, Anne;
- Sanatani, Shubhayan;
- Gelmon, Karen A.;
- Bernstein, Daniel;
- Hayden, Michael R.;
- Amstutz, Ursula;
- Carleton, Bruce C.
Publication type:
Article
Urinary TIMP-2*IGFBP-7 to diagnose acute kidney injury in children receiving cisplatin.
Published in:
Pediatric Nephrology, 2024, v. 39, n. 1, p. 269, doi. 10.1007/s00467-023-06007-8
By:
- Chui, Hayton;
- McMahon, Kelly R.;
- Rassekh, Shahrad Rod;
- Schultz, Kirk R.;
- Blydt-Hansen, Tom D.;
- Mammen, Cherry;
- Pinsk, Maury;
- Cuvelier, Geoffrey D. E.;
- Carleton, Bruce C.;
- Tsuyuki, Ross T.;
- Ross, Colin J. D.;
- Devarajan, Prasad;
- Huynh, Louis;
- Yordanova, Mariya;
- Crépeau-Hubert, Frédérik;
- Wang, Stella;
- Cockovski, Vedran;
- Palijan, Ana;
- Zappitelli, Michael;
- Baruchel, Sylvain
Publication type:
Article
Acute kidney injury during cisplatin therapy and associations with kidney outcomes 2 to 6 months post-cisplatin in children: a multi-centre, prospective observational study.
Published in:
Pediatric Nephrology, 2023, v. 38, n. 5, p. 1667, doi. 10.1007/s00467-022-05745-5
By:
- McMahon, Kelly R.;
- Lebel, Asaf;
- Rassekh, Shahrad Rod;
- Schultz, Kirk R.;
- Blydt-Hansen, Tom D.;
- Cuvelier, Geoffrey D. E.;
- Mammen, Cherry;
- Pinsk, Maury;
- Carleton, Bruce C.;
- Tsuyuki, Ross T.;
- Ross, Colin J. D.;
- Huynh, Louis;
- Yordanova, Mariya;
- Crépeau-Hubert, Frédérik;
- Wang, Stella;
- Palijan, Ana;
- Lee, Jasmine;
- Boyko, Debbie;
- Zappitelli, Michael
Publication type:
Article
Cellular metabolism constrains innate immune responses in early human ontogeny.
Published in:
Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07215-9
By:
- Kan, Bernard;
- Michalski, Christina;
- Fu, Helen;
- Au, Hilda H. T.;
- Lee, Kelsey;
- Marchant, Elizabeth A.;
- Cheng, Maye F.;
- Anderson-Baucum, Emily;
- Aharoni-Simon, Michal;
- Tilley, Peter;
- Mirmira, Raghavendra G.;
- Ross, Colin J.;
- Luciani, Dan S.;
- Jan, Eric;
- Lavoie, Pascal M.
Publication type:
Article
RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1301, doi. 10.1038/ejhg.2014.293
By:
- Janer, Alexandre;
- van Karnebeek, Clara DM;
- Sasarman, Florin;
- Antonicka, Hana;
- Al Ghamdi, Malak;
- Shyr, Casper;
- Dunbar, Mary;
- Stockler-Ispiroglu, Sylvia;
- Ross, Colin J;
- Vallance, Hilary;
- Dionne, Janis;
- Wasserman, Wyeth W;
- Shoubridge, Eric A
Publication type:
Article
HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.
Published in:
European Journal of Human Genetics, 2011, v. 19, n. 5, p. 561, doi. 10.1038/ejhg.2010.229
By:
- Warby, Simon C.;
- Visscher, Henk;
- Collins, Jennifer A.;
- Doty, Crystal N.;
- Carter, Catherine;
- Butland, Stefanie L.;
- Hayden, Anna R.;
- Kanazawa, Ichiro;
- Ross, Colin J.;
- Hayden, Michael R.
Publication type:
Article
Paediatric cardio-oncology: epidemiology, screening, prevention, and treatment.
Published in:
Cardiovascular Research, 2019, v. 115, n. 5, p. 922, doi. 10.1093/cvr/cvz031
By:
- Chow, Eric J;
- Leger, Kasey J;
- Bhatt, Neel S;
- Mulrooney, Daniel A;
- Ross, Colin J;
- Aggarwal, Sanjeev;
- Bansal, Neha;
- Ehrhardt, Matthew J;
- Armenian, Saro H;
- Scott, Jessica M;
- Hong, Borah
Publication type:
Article
Assessing the role of adolescent hormonal contraceptive use on risk for depression: a 3-year longitudinal study protocol.
Published in:
2022
By:
- Zareian, Bita;
- Anderl, Christine;
- LeMoult, Joelle;
- Galea, Liisa A. M.;
- Prior, Jerilynn C.;
- Rights, Jason D.;
- Ross, Colin J.;
- Ge, Sabrina;
- Hayward, Annie C.;
- Chen, Frances S.
Publication type:
journal article
Pharmacogenomic testing: Enhancing personalized medication use for patients.
Published in:
2020
By:
- Loucks, Catrina M.;
- Groeneweg, Gabriella;
- Roy, Carl;
- Lee, David K.;
- Rieder, Michael J.;
- Lebel, Denis;
- Ito, Shinya;
- Ross, Colin J.;
- Carleton, Bruce C.
Publication type:
journal article
Patient‐specific genetic factors predict treatment failure in sofosbuvir‐treated patients with chronic hepatitis C.
Published in:
Liver International, 2022, v. 42, n. 4, p. 796, doi. 10.1111/liv.15175
By:
- Loucks, Catrina M.;
- Lin, Jennifer J.;
- Trueman, Jessica N.;
- Drögemöller, Britt I.;
- Wright, Galen E. B.;
- Chang, Wan‐Chun;
- Li, Kathy H.;
- Yoshida, Eric M.;
- Ford, Jo‐Ann;
- Lee, Samuel S.;
- Crotty, Pam;
- Kim, Richard B.;
- Al‐Judaibi, Bandar;
- Schwarz, Ute I.;
- Ramji, Alnoor;
- Farivar, Jeanette F.;
- Tam, Edward;
- Walston, Lori Lee;
- Ross, Colin J. D.;
- Carleton, Bruce C.
Publication type:
Article
Promoting Neuroplasticity for Motor Rehabilitation After Stroke: Considering the Effects of Aerobic Exercise and Genetic Variation on Brain-Derived Neurotrophic Factor.
Published in:
Physical Therapy, 2013, v. 93, n. 12, p. 1707, doi. 10.2522/ptj.20130053
By:
- Mang, Cameron S.;
- Campbell, Kristin L.;
- Ross, Colin J. D.;
- Boyd, Lara A.
Publication type:
Article
Epidemiologic Characteristics of Acute Kidney Injury During Cisplatin Infusions in Children Treated for Cancer.
Published in:
JAMA Network Open, 2020, v. 3, n. 5, p. e203639, doi. 10.1001/jamanetworkopen.2020.3639
By:
- McMahon, Kelly R.;
- Rassekh, Shahrad Rod;
- Schultz, Kirk R.;
- Blydt-Hansen, Tom;
- Cuvelier, Geoffrey D. E.;
- Mammen, Cherry;
- Pinsk, Maury;
- Carleton, Bruce C.;
- Tsuyuki, Ross T.;
- Ross, Colin J. D.;
- Palijan, Ana;
- Huynh, Louis;
- Yordanova, Mariya;
- Crépeau-Hubert, Frédérik;
- Wang, Stella;
- Boyko, Debbie;
- Zappitelli, Michael
Publication type:
Article
Neonatal T Helper 17 Responses Are Skewed Towards an Immunoregulatory Interleukin-22 Phenotype.
Published in:
Frontiers in Immunology, 2021, v. 12, p. N.PAG, doi. 10.3389/fimmu.2021.655027
By:
- Razzaghian, Hamid R.;
- Sharafian, Zohreh;
- Sharma, Ashish A.;
- Boyce, Guilaine K.;
- Lee, Kelsey;
- Da Silva, Rachel;
- Orban, Paul C.;
- Sekaly, Rafick-Pierre;
- Ross, Colin J.;
- Lavoie, Pascal M.
Publication type:
Article
Different Disease Endotypes in Phenotypically Similar Vasculitides Affecting Small-to-Medium Sized Blood Vessels.
Published in:
Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.638571
By:
- Gill, Erin E.;
- Smith, Maren L.;
- Gibson, Kristen M.;
- Morishita, Kimberly A.;
- Lee, Amy H. Y.;
- Falsafi, Reza;
- Graham, Jinko;
- Foell, Dirk;
- Benseler, Susanne M.;
- Ross, Colin J.;
- Luqmani, Raashid A.;
- Cabral, David A.;
- Hancock, Robert E. W.;
- Brown, Kelly L.
Publication type:
Article
Autoantibodies Against Lysosome Associated Membrane Protein-2 (LAMP-2) in Pediatric Chronic Primary Systemic Vasculitis.
Published in:
Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.624758
By:
- Gibson, Kristen M.;
- Kain, Renate;
- Luqmani, Raashid A.;
- Ross, Colin J.;
- Cabral, David A.;
- Brown, Kelly L.
Publication type:
Article
A cross-sectional study of the relationship between CYP2D6 and CYP2C19 variations and depression symptoms, for women taking SSRIs during pregnancy.
Published in:
Archives of Women's Mental Health, 2022, v. 25, n. 2, p. 355, doi. 10.1007/s00737-021-01149-w
By:
- Hippman, Catriona;
- Slomp, Caitlin;
- Morris, Emily;
- Batallones, Rolan;
- Inglis, Angela;
- Carrion, Prescilla;
- Brain, Ursula;
- Higginson, Michelle;
- Wright, Galen E. B.;
- Balneaves, Lynda G.;
- Ryan, Deirdre;
- Nislow, Corey;
- Ross, Colin J. D.;
- Gaedigk, Andrea;
- Oberlander, Tim F.;
- Austin, Jehannine
Publication type:
Article
The <i>Salmonella</i> Type III Effector SspH2 Specifically Exploits the NLR Co-chaperone Activity of SGT1 to Subvert Immunity.
Published in:
PLoS Pathogens, 2013, v. 9, n. 7, p. 1, doi. 10.1371/journal.ppat.1003518
By:
- Bhavsar, Amit P.;
- Brown, Nat F.;
- Stoepel, Jan;
- Wiermer, Marcel;
- Martin, Dale D. O.;
- Hsu, Karolynn J.;
- Imami, Koshi;
- Ross, Colin J.;
- Hayden, Michael R.;
- Foster, Leonard J.;
- Li, Xin;
- Hieter, Phil;
- Finlay, B. Brett
Publication type:
Article
Experiences With Genetic Counseling, Testing, and Diagnosis Among Adolescents With a Genetic Condition: A Scoping Review.
Published in:
JAMA Pediatrics, 2022, v. 176, n. 2, p. 185, doi. 10.1001/jamapediatrics.2021.4290
By:
- Wainstein, Tasha;
- Marshall, Sheila K.;
- Ross, Colin J. D.;
- Virani, Alice K.;
- Austin, Jehannine C.;
- Elliott, Alison M.
Publication type:
Article
Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease.
Published in:
Human Molecular Genetics, 2020, v. 29, n. 16, p. 2788, doi. 10.1093/hmg/ddaa184
By:
- Wright, Galen E. B.;
- Caron, Nicholas S.;
- Ng, Bernard;
- Casal, Lorenzo;
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- Ross, Colin J. D.;
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Publication type:
Article
VKORC1 and CYP2C9 genotypes are predictors of warfarin-related outcomes in children.
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Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1055, doi. 10.1002/pbc.24932
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Publication type:
Article
907. Gene Therapy for Genetic Lipoprotein Lipase (LPL) Deficiency; an Update
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2005
By:
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- Sierts, Jeroen A.;
- Ross, Colin J.;
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- de Jong, Albertine;
- Dijkhuizen, Paul;
- Hermens, Wim;
- Twisk, Jaap;
- Kastelein, John J.;
- Kuivenhoven, Jan Albert;
- Meulenberg, Janneke M.
Publication type:
Abstract
Identification of Novel Adenosine Deaminase 2 Gene Variants and Varied Clinical Phenotype in Pediatric Vasculitis.
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Arthritis & Rheumatology, 2019, v. 71, n. 10, p. 1747, doi. 10.1002/art.40913
By:
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- Han, Xiaohua;
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- Benseler, Susanne;
- Luqmani, Rashid;
- Yeung, Rae S. M.;
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- Bohm, Marek;
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- Ross, Colin J.;
- Cabral, David A.;
- Brown, Kelly L.
Publication type:
Article
Implementation of pharmacogenetic testing in oncology: DPYD-guided dosing to prevent fluoropyrimidine toxicity in British Columbia.
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Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1257745
By:
- Wu, Angela;
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- Hughesman, Curtis;
- Young, Sean;
- Lohrisch, Caroline;
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Publication type:
Article
Pharmacogenomic Variability of Oral Baclofen Clearance and Clinical Response in Children With Cerebral Palsy.
Published in:
2017
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- McLaughlin, Matthew J;
- He, Yang;
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- Ross, Colin J D;
- Gaedigk, Andrea;
- Lewandowski, Andrew;
- Dai, Hongying;
- Jusko, William J;
- Leeder, J Steven
Publication type:
journal article
All-trans retinoic acid (ATRA) regulates key genes in the RARG-TOP2B pathway and reduces anthracycline-induced cardiotoxicity.
Published in:
PLoS ONE, 2022, v. 17, n. 11, p. 1, doi. 10.1371/journal.pone.0276541
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- Miao, Fudan;
- Soliman, Hesham;
- Carleton, Bruce C.;
- Ross, Colin J. D.
Publication type:
Article
Analyses of Adverse Drug Reactions–Nationwide Active Surveillance Network: Canadian Pharmacogenomics Network for Drug Safety Database.
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Journal of Clinical Pharmacology, 2019, v. 59, n. 3, p. 356, doi. 10.1002/jcph.1336
By:
- Tanoshima, Reo;
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- Trueman, Jessica N.;
- Drögemöller, Britt I.;
- Wright, Galen E. B.;
- Hasbullah, Jafar S.;
- Groeneweg, Gabriella S. S.;
- Ross, Colin J. D.;
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Publication type:
Article
Genetic Markers of Cisplatin-Induced Hearing Loss in Children.
Published in:
Clinical Advances in Hematology & Oncology, 2014, v. 12, n. 8, p. 527
By:
- Carleton, Bruce C.;
- Ross, Colin J.;
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