This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of British Columbia directory, so their courses and email address may be missing. Find their university profile.
Research
Latest papers
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
European journal of pediatrics · 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency.
Molecular genetics and metabolism reports · 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency.
Molecular genetics and metabolism reports · 2019
Latest funding
- $105,000
Intersecting genealogic and genetic approaches to identify a mutation causing autosomal dominant, non-syndromic strabismus and its general application to precision medicine
CIHR · 2015 · Supervisor
- $510,470
Amniotic Fluid Virome and Preterm Birth
CIHR · 2013 · Nominated PI
- $99,000
Fracture, Bone Health and Oxidative Stress: Is Polycystic Ovary Syndrome Premature Aging?
CIHR · 2010 · Co-investigator
6 publications.
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
Elliott AM, du Souich C, Lehman A, Guella I, Evans DM, Candido T, Tooman L, Armstrong L, Clarke L, Gibson W, Gill H, Lavoie PM, Lewis S, McKinnon ML, Nikkel SM, Patel M, Solimano A, Synnes A, Ting J, van Allen M, Christilaw J, Farrer MJ, Friedman JM, Osiovich H
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiency.
Apatean D, Rakic B, Brunel-Guitton C, Hendson G, Bai R, Sargent MA, Lavoie PM, Patel M, Stockler-Ipsiroglu S
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency.
Apatean D, Rakic B, Brunel-Guitton C, Hendson G, Bai R, Sargent MA, Lavoie PM, Patel M, Stockler-Ipsiroglu S
GeneYenta: a phenotype-based rare disease case matching tool based on online dating algorithms for the acceleration of exome interpretation.
Gottlieb MM, Arenillas DJ, Maithripala S, Maurer ZD, Tarailo Graovac M, Armstrong L, Patel M, van Karnebeek C, Wasserman WW
Diffuse angiopathy in Adams-Oliver syndrome associated with truncating DOCK6 mutations.
Lehman A, Stittrich AB, Glusman G, Zong Z, Li H, Eydoux P, Senger C, Lyons C, Roach JC, Patel M
A variant of unknown significance in the GLA gene causing diagnostic uncertainty in a young female with isolated hypertrophic cardiomyopathy.
Al-Thihli K, Ebrahim H, Hughes DA, Patel M, Tipple M, Salvarinova R, Gardiner J, Vallance H, Waters PJ
Intersecting genealogic and genetic approaches to identify a mutation causing autosomal dominant, non-syndromic strabismus and its general application to precision medicine
Principal investigators: Ye, Xin
Keywords: Family Study; Genealogy; Genomics; High Throughput Sequencing; Strabismus
Amniotic Fluid Virome and Preterm Birth
Principal investigators: Patel, Millan
Keywords: Case Control Study; Inflammation; Intra-Amniotic Infection; Metagenomics; Microbiome; Preterm Birth; Preterm Labor; Virome
Fracture, Bone Health and Oxidative Stress: Is Polycystic Ovary Syndrome Premature Aging?
Principal investigators: Prior, Jerilynn C
Keywords: Aging; Biomarkers For Bone Fragility; Bone Mineral Density; Dna Damage; Inflammation; Insulin Resistance; N-Acetyl Cysteine; Oxidative Stress; Polycystic Ovary Syndrome; Telomere Length
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
- Jan Christilaw and Millan Patel: 1 shared paper
- Jan Christilaw and William Gibson: 1 shared paper
- Clara van Karnebeek and Millan Patel: 1 shared paper
- Millan Patel and William Gibson: 1 shared paper
- Pediatrics
- Family Practice
- Medical Genetics
- 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.
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