Peter Kannu

ScholarGPS® ID: 21282657738775

Affiliation

University of Alberta, Edmonton, Canada

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Metrics Summary

Publication Count

Predicted Citations

1,909

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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Integrative analysis of Lunatic Fringe variants associated with spondylocostal dysostosis type‐ III (journal article) Wengryn, Parker \| Fenrich, Felicity \| Silveira, Karina da Costa \| Oborn, Connor \| Mizumoto, Shuji \| Beke, Alexander \| Soltys, Carrie‐Lynn \| Yamada, Shuhei \| Kannu, Peter The FASEB Journal, volume 38, issue 13 (2024). 10.1096/fj.202302651RR Cite \| Source
P329: A homozygous start-loss mutation in TERF1 causes a syndrome associated with long telomeres (journal article) Anandampillai, Tanvi \| Kannu, Peter \| Dror, Yigal \| Mendoza-Londono, Roberto \| Lara-Corrales, Irene \| Wang, Yiming Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101223 Cite \| Source
CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence (journal article) Silveira, Karina C. \| Fonseca, Inara Chacon \| Oborn, Connor \| Wengryn, Parker \| Ghafoor, Saima \| Beke, Alexander \| Dreseris, Ema S. \| Wong, Cassandra \| Iacovone, Aline \| Soltys, Carrie-Lynn \| ... \| Kannu, Peter Human Genetics, volume 142, issue 11, pages 1571-1586 (2023). 10.1007/s00439-023-02598-2 Cited by (2) \| Cite \| Source
Functional Characterization of Novel Lunatic Fringe Variants in Spondylocostal Dysostosis Type-III with Scoliosis (journal article) Wengryn, Parker \| Silveira, Karina da Costa \| Oborn, Connor \| Soltys, Carrie-Lynn \| Beke, Alexander \| Chacon-Fonseca, Inara \| Damseh, Nadirah \| Rodriguez, Marco Quesada \| Badilla-Porras, Ramses \| Kannu, Peter Human Mutation, volume 2023 (2023). 10.1155/2023/5989733 Cited by (1) \| Cite \| Source
Spondyloepimetaphyseal dysplasia with joint laxity type 2: Aggregating the literature and reporting on the life of a 66‐year‐old man (journal article) Beke, Alexander \| da Costa Silveira, Karina \| Athey, Taryn \| Kannu, Peter American Journal of Medical Genetics Part C: Seminars in Medical Genetics, volume 193, issue 2, pages 188-192 (2023). 10.1002/ajmg.c.32053 Cited by (2) \| Cite \| Source
The Effects of Palovarotene in Patients with Fibrodysplasia Ossificans Progressiva: A Plain Language Summary (journal article) Pignolo, Robert J \| Hsiao, Edward C \| Mukaddam, Mona Al \| Baujat, Geneviève \| Berglund, Staffan K \| Brown, Matthew A \| Cheung, Angela M \| Cunto, Carmen De \| Delai, Patricia \| Haga, Nobuhiko \| ... \| Kaplan, Frederick S Future Rare Diseases, volume 3, issue 1 (2023). 10.2217/frd-2022-0015 Cite \| Source
Reduction of New Heterotopic Ossification ( HO ) in the Open‐Label , Phase 3 MOVE Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva ( FOP ) (journal article) Pignolo, Robert J. \| Hsiao, Edward C. \| Al Mukaddam, Mona \| Baujat, Geneviève \| Berglund, Staffan K. \| Brown, Matthew A. \| Cheung, Angela M. \| De Cunto, Carmen \| Delai, Patricia \| Haga, Nobuhiko \| ... \| Kaplan, Frederick S. Journal of Bone and Mineral Research, volume 38, issue 3, pages 381-394 (2023). 10.1002/jbmr.4762 Cited by (24) \| Cite \| Source
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinics (journal article) Mainali, Apurba \| Athey, Taryn \| Bahl, Shalini \| Hung, Clara \| Caluseriu, Oana \| Chan, Alicia \| Eaton, Alison \| Ghai, Shailly Jain \| Kannu, Peter \| MacPherson, Melissa \| ... \| Mercimek‐Andrews, Saadet American Journal of Medical Genetics Part A, volume 191, issue 2, pages 510-517 (2023). 10.1002/ajmg.a.63053 Cited by (5) \| Cite \| Source
Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease (journal article) Reis, Linda M. \| Atilla, Huban \| Kannu, Peter \| Schneider, Adele \| Thompson, Samuel \| Bardakjian, Tanya \| Semina, Elena V. Genes, volume 14, issue 1, pages 216- (2023). 10.3390/genes14010216 Cited by (2) \| Cite \| Source
Prenatal Genetic Testing in the Era of Next Generation Sequencing: A One-Center Canadian Experience (journal article) Almubarak, Asra \| Zhang, Dan \| Kosak, Mackenzie \| Rathwell, Sarah \| Doonanco, Jasmine \| Eaton, Alison J. \| Kannu, Peter \| Lazier, Joanna \| Lui, Monique \| Niederhoffer, Karen Y. \| ... \| Caluseriu, Oana Genes, volume 13, issue 11, pages 2019- (2022). 10.3390/genes13112019 Cited by (1) \| Cite \| Source
Exome Sequencing Identifies a Biallelic GALNS Variant (p.Asp233Asn) Causing Mucopolysaccharidosis Type IVA in a Pakistani Consanguineous Family (journal article) Ghafoor, Saima \| Silveira, Karina da Costa \| Qamar, Raheel \| Azam, Maleeha \| Kannu, Peter Genes, volume 13, issue 10, pages 1743- (2022). 10.3390/genes13101743 Cited by (3) \| Cite \| Source
Value of a café‐au‐lait macules screening clinic: Experience from The Hospital for Sick Children in Toronto (journal article) Albaghdadi, Mohammed \| Berseneva, Maria \| Pennal, Alexandra \| Wan, Stephanie \| Matviychuk, Diana \| Shugar, Andrea \| Kannu, Peter \| Lara‐Corrales, Irene Pediatric Dermatology, volume 39, issue 2, pages 205-210 (2022). 10.1111/pde.14947 Cited by (1) \| Cite \| Source
Prevalence of Choroidal Abnormalities and Lisch Nodules in Children Meeting Clinical and Molecular Diagnosis of Neurofibromatosis Type 1 (journal article) Flores Pimentel, Mariana \| Heath, Anna \| Wan, Michael J. \| Hussein, Rowaida \| Leahy, Kate E. \| MacDonald, Heather \| Tavares, Erika \| VandenHoven, Cynthia \| MacNeill, Katelyn \| Kannu, Peter \| ... \| Vincent, Ajoy Translational Vision Science & Technology, volume 11, issue 2, pages 10- (2022). 10.1167/tvst.11.2.10 Cited by (5) \| Cite \| Source
Lost bones: differential diagnosis of acro-osteolysis seen by the pediatric rheumatologist (journal article) Limenis, Elizaveta \| Stimec, Jennifer \| Kannu, Peter \| Laxer, Ronald M. Pediatric Rheumatology, volume 19, issue 1 (2021). 10.1186/s12969-021-00596-0 Cited by (10) \| Cite \| Source
Diagnostic utility of next-generation sequence genetic panel testing in children presenting with a clinically significant fracture history (journal article) Harrington, Jennifer \| AlSubaihin, Abdulmajeed \| Dupuis, Lucie \| Kannu, Peter \| Mendoza-Londono, Roberto \| Howard, Andrew Archives of Osteoporosis, volume 16, issue 1 (2021). 10.1007/s11657-021-00943-4 Cited by (2) \| Cite \| Source
Extended Phenotyping and Functional Validation Facilitate Diagnosis of a Complex Patient Harboring Genetic Variants in MCCC1 and GNB5 Causing Overlapping Phenotypes (journal article) Shao, Zhuo \| Masuho, Ikuo \| Tumber, Anupreet \| Maynes, Jason T. \| Tavares, Erika \| Ali, Asim \| Hewson, Stacy \| Schulze, Andreas \| Kannu, Peter \| Martemyanov, Kirill A. \| Vincent, Ajoy Genes, volume 12, issue 9, pages 1352- (2021). 10.3390/genes12091352 Cited by (3) \| Cite \| Source
Infigratinib in Children With Achondroplasia (ACH): Design of PROPEL2 - A Phase 2, Open-Label, Dose-Escalation and Dose-Expansion Study (journal article) Savarirayan, Ravi \| Kannu, Peter \| Dambkowski, Carl L \| Rogoff, Daniela \| Irving, Melita Journal of the Endocrine Society, volume 5, issue Supplement_1, pages A667-A668 (2021). 10.1210/jendso/bvab048.1363 Cite \| Source
ELOVL4 with erythrokeratoderma: A pediatric case and emerging genodermatosis (journal article) Croitoru, David \| Lu, Justin D. \| Lara‐Corrales, Irene \| Kannu, Peter \| Pope, Elena American Journal of Medical Genetics Part A, volume 185, issue 5, pages 1619-1623 (2021). 10.1002/ajmg.a.62136 Cited by (3) \| Cite \| Source
Improving the Diagnosis of Fibrodysplasia Ossificans Progressiva (journal article) Kannu, Peter \| Levy, Charles E. The Journal of Pediatrics, volume 232 (2021). 10.1016/j.jpeds.2021.02.036 Cited by (1) \| Cite \| Source
Hardened Hope: Care Advances for Fibrodysplasia Ossificans Progressiva (journal article) Kannu, Peter \| Levy, Charles E. The Journal of Pediatrics, volume 232 (2021). 10.1016/j.jpeds.2021.02.035 Cited by (1) \| Cite \| Source