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Research
Latest papers
Optimising the process for conducting scoping reviews.
BMJ evidence-based medicine · 2021
Scoping review of symptoms in children with rare, progressive, life-threatening disorders.
BMJ supportive & palliative care · 2020
BRIGHT Coaching: A Randomized Controlled Trial on the Effectiveness of a Developmental Coach System to Empower Families of Children With Emerging Developmental Delay.
Frontiers in pediatrics · 2019
Latest funding
- $50,000
A Scoping Review to Examine the Extent and Quality of Literature on Symptoms in Children with Rare, Progressive Disorders
CIHR · 2014 · Principal investigator
6 publications.
Optimising the process for conducting scoping reviews.
Pawliuk C, Brown HL, Widger K, Dewan T, Hermansen AM, Grégoire MC, Steele R, Siden HH
Scoping review of symptoms in children with rare, progressive, life-threatening disorders.
Pawliuk C, Widger K, Dewan T, Brander G, Brown HL, Hermansen AM, Grégoire MC, Steele R, Siden HH
BRIGHT Coaching: A Randomized Controlled Trial on the Effectiveness of a Developmental Coach System to Empower Families of Children With Emerging Developmental Delay.
Majnemer A, O'Donnell M, Ogourtsova T, Kasaai B, Ballantyne M, Cohen E, Collet JP, Dewan T, Elsabbagh M, Hanlon-Dearman A, Filliter JH, Lach L, McElroy T, McGrath P, McKellin W, Miller A, Patel H, Rempel G, Shevell M, Wittmeier K, Parent-Panel
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.
Cogné B, Ehresmann S, Beauregard-Lacroix E, Rousseau J, Besnard T, Garcia T, Petrovski S, Avni S, McWalter K, Blackburn PR, Sanders SJ, Uguen K, Harris J, Cohen JS, Blyth M, Lehman A, Berg J, Li MH, Kini U, Joss S, von der Lippe C, Gordon CT, Humberson JB, Robak L, Scott DA, Sutton VR, Skraban CM, Johnston JJ, Poduri A, Nordenskjöld M, Shashi V, Gerkes EH, Bongers EMHF, Gilissen C, Zarate YA, Kvarnung M, Lally KP, Kulch PA, Daniels B, Hernandez-Garcia A, Stong N, McGaughran J, Retterer K, Tveten K, Sullivan J, Geisheker MR, Stray-Pedersen A, Tarpinian JM, Klee EW, Sapp JC, Zyskind J, Holla ØL, Bedoukian E, Filippini F, Guimier A, Picard A, Busk ØL, Punetha J, Pfundt R, Lindstrand A, Nordgren A, Kalb F, Desai M, Ebanks AH, Jhangiani SN, Dewan T, Coban Akdemir ZH, Telegrafi A, Zackai EH, Begtrup A, Song X, Toutain A, Wentzensen IM, Odent S, Bonneau D, Latypova X, Deb W, CAUSES Study, Redon S, Bilan F, Legendre M, Troyer C, Whitlock K, Caluseriu O, Murphree MI, Pichurin PN, Agre K, Gavrilova R, Rinne T, Park M, Shain C, Heinzen EL, Xiao R, Amiel J, Lyonnet S, Isidor B, Biesecker LG, Lowenstein D, Posey JE, Denommé-Pichon AS, Deciphering Developmental Disorders study, Férec C, Yang XJ, Rosenfeld JA, Gilbert-Dussardier B, Audebert-Bellanger S, Redon R, Stessman HAF, Nellaker C, Yang Y, Lupski JR, Goldstein DB, Eichler EE, Bolduc F, Bézieau S, Küry S, Campeau PM
NANS-mediated synthesis of sialic acid is required for brain and skeletal development.
van Karnebeek CD, Bonafé L, Wen XY, Tarailo-Graovac M, Balzano S, Royer-Bertrand B, Ashikov A, Garavelli L, Mammi I, Turolla L, Breen C, Donnai D, Cormier-Daire V, Heron D, Nishimura G, Uchikawa S, Campos-Xavier B, Rossi A, Hennet T, Brand-Arzamendi K, Rozmus J, Harshman K, Stevenson BJ, Girardi E, Superti-Furga G, Dewan T, Collingridge A, Halparin J, Ross CJ, Van Allen MI, Rossi A, Engelke UF, Kluijtmans LA, van der Heeft E, Renkema H, de Brouwer A, Huijben K, Zijlstra F, Heise T, Boltje T, Wasserman WW, Rivolta C, Unger S, Lefeber DJ, Wevers RA, Superti-Furga A
Exome Sequencing and the Management of Neurometabolic Disorders.
Tarailo-Graovac M, Shyr C, Ross CJ, Horvath GA, Salvarinova R, Ye XC, Zhang LH, Bhavsar AP, Lee JJ, Drögemöller BI, Abdelsayed M, Alfadhel M, Armstrong L, Baumgartner MR, Burda P, Connolly MB, Cameron J, Demos M, Dewan T, Dionne J, Evans AM, Friedman JM, Garber I, Lewis S, Ling J, Mandal R, Mattman A, McKinnon M, Michoulas A, Metzger D, Ogunbayo OA, Rakic B, Rozmus J, Ruben P, Sayson B, Santra S, Schultz KR, Selby K, Shekel P, Sirrs S, Skrypnyk C, Superti-Furga A, Turvey SE, Van Allen MI, Wishart D, Wu J, Wu J, Zafeiriou D, Kluijtmans L, Wevers RA, Eydoux P, Lehman AM, Vallance H, Stockler-Ipsiroglu S, Sinclair G, Wasserman WW, van Karnebeek CD
A Scoping Review to Examine the Extent and Quality of Literature on Symptoms in Children with Rare, Progressive Disorders
Principal investigators: Siden, Harold B; Dewan, Tammie
Keywords: Chromosomal Conditions; Complex Care; Metabolic Disease; Neurologic Conditions; Pediatric Palliative Care; Pediatrics; Rare Disorders; Scoping Review; Symptom Assessment; Symptom Management
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Annette Majnemer and Kristy Wittmeier: 7 shared papers
- Annette Majnemer and Lucyna Lach: 6 shared papers
- Patrick McGrath and Lucyna Lach: 2 shared papers
- David Wishart and Tammie Dewan: 1 shared paper
- David Wishart and Janis Dionne: 1 shared paper
- Eyal Cohen and Patrick McGrath: 1 shared paper
- Eyal Cohen and Mayada Elsabbagh: 1 shared paper
- Eyal Cohen and Annette Majnemer: 1 shared paper
- Eyal Cohen and Ana Hanlon-Dearman: 1 shared paper
- Eyal Cohen and Kristy Wittmeier: 1 shared paper
- Eyal Cohen and Tammie Dewan: 1 shared paper
- Eyal Cohen and Lucyna Lach: 1 shared paper
- Patrick McGrath and Mayada Elsabbagh: 1 shared paper
- Patrick McGrath and Ana Hanlon-Dearman: 1 shared paper
- Patrick McGrath and Kristy Wittmeier: 1 shared paper
- Patrick McGrath and Tammie Dewan: 1 shared paper
- Mayada Elsabbagh and Annette Majnemer: 1 shared paper
- Mayada Elsabbagh and Ana Hanlon-Dearman: 1 shared paper
- Mayada Elsabbagh and Tammie Dewan: 1 shared paper
- Annette Majnemer and Tammie Dewan: 1 shared paper
- Annette Majnemer and François Bolduc: 1 shared paper
- Ana Hanlon-Dearman and Tammie Dewan: 1 shared paper
- Kristy Wittmeier and Tammie Dewan: 1 shared paper
- Tammie Dewan and Xiang-Jiao Yang: 1 shared paper
- Tammie Dewan and Lucyna Lach: 1 shared paper
- Tammie Dewan and François Bolduc: 1 shared paper
- Tammie Dewan and Xiao-Yan Wen: 1 shared paper
- Tammie Dewan and Janis Dionne: 1 shared paper
- Xiang-Jiao Yang and François Bolduc: 1 shared paper
- Medicine
- Pediatrics
- Community Health Sciences
- Neurology
- Biological Sciences
- Pediatrics and Child Health
- Other
Co-authors at University of British Columbia, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Xiang-Jiao Yang
Medicine
1 shared papers, latest 2019
Lucyna Lach
Faculty
1 shared papers, latest 2019
François Bolduc
Pediatrics
1 shared papers, latest 2019
Xiao-Yan Wen
Medicine
1 shared papers, latest 2016
Janis Dionne
Pediatrics
1 shared papers, latest 2016
David Wishart
Biological Sciences
1 shared papers, latest 2016
Eyal Cohen
Medicine
1 shared papers, latest 2019
Patrick McGrath
Faculty
1 shared papers, latest 2019
Mayada Elsabbagh
Faculty
1 shared papers, latest 2019
Annette Majnemer
Neurology
1 shared papers, latest 2019
Ana Hanlon-Dearman
Community Health Sciences
1 shared papers, latest 2019
Kristy Wittmeier
Pediatrics and Child Health
1 shared papers, latest 2019
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