Sharan Goobie

924 total citations
29 papers, 504 citations indexed

About

Sharan Goobie is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Sharan Goobie has authored 29 papers receiving a total of 504 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Immunology. Recurrent topics in Sharan Goobie's work include Immunodeficiency and Autoimmune Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Blood disorders and treatments (5 papers). Sharan Goobie is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (7 papers), Genomics and Rare Diseases (5 papers) and Blood disorders and treatments (5 papers). Sharan Goobie collaborates with scholars based in Canada, United States and Netherlands. Sharan Goobie's co-authors include Jodi Morrison, Johanna M. Rommens, Lynda Ellis, Peter R. Durie, Hedy Ginzberg, M. Popović, Craig Campbell, Takuya Fujiwara, Kenneth Morgan and Kym M. Boycott and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Sharan Goobie

27 papers receiving 485 citations

Peers

Sharan Goobie
Rehab Ali Qatar
Rebecca I. Torene United States
Rachel Sayuri Honjo Brazil
Alina Kurolap Israel
Robert L. Conway United States
SG Ahmed Nigeria
Frederick V. Schaefer United States
Jens Gertow Sweden
Alexis L. Franks United States
Christin Collins United States
Rehab Ali Qatar
Sharan Goobie
Citations per year, relative to Sharan Goobie Sharan Goobie (= 1×) peers Rehab Ali

Countries citing papers authored by Sharan Goobie

Since Specialization
Citations

This map shows the geographic impact of Sharan Goobie's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sharan Goobie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sharan Goobie more than expected).

Fields of papers citing papers by Sharan Goobie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sharan Goobie. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sharan Goobie. The network helps show where Sharan Goobie may publish in the future.

Co-authorship network of co-authors of Sharan Goobie

This figure shows the co-authorship network connecting the top 25 collaborators of Sharan Goobie. A scholar is included among the top collaborators of Sharan Goobie based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sharan Goobie. Sharan Goobie is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Richer, Julie, Sharan Goobie, Ingrid M.B.H. van de Laar, et al.. (2025). Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals. Journal of Medical Genetics. 62(3). 199–205.
2.
Yang, Ping, Chitra Prasad, Simon A. Levin, et al.. (2021). De novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures. Frontiers in Neurology. 12. 804078–804078. 3 indexed citations
3.
Ganguly, Jacky, et al.. (2021). Myoclonus‐Dystonia Presentation of ATM Gene Mutation in a Canadian Mennonite. Movement Disorders Clinical Practice. 9(2). 264–267. 4 indexed citations
4.
O’Connor, Kathleen, Sharan Goobie, Greg Moran, et al.. (2018). Psychosocial impact on mothers receiving expanded newborn screening results. European Journal of Human Genetics. 26(4). 477–484. 19 indexed citations
5.
Jain, Puneet, Danielle M. Andrade, Elizabeth Donner, et al.. (2018). Development of Criteria for Epilepsy Genetic Testing in Ontario, Canada. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 46(1). 7–13. 18 indexed citations
6.
Upton, Julia, et al.. (2017). Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1. Journal of Clinical Immunology. 38(1). 88–95. 37 indexed citations
7.
Farhan, Sali M.K., et al.. (2016). KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connection. American Journal of Medical Genetics Part A. 173(1). 183–189. 14 indexed citations
8.
Prasad, Chitra, Melanie Napier, Sharan Goobie, et al.. (2015). Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007–2014). Molecular Genetics and Metabolism. 116(3). 146–151. 19 indexed citations
9.
Meijer, Inge A., Cynthia V. Bourassa, Nancy D. Merner, et al.. (2013). A VAMP1 Mutation Causes Chromosome 12p13 Hereditary Spastic Ataxia in Newfoundland Families (S43.002). Neurology. 80(7_supplement).
10.
Yoon, Grace, Berivan Baskin, Mark A. Tarnopolsky, et al.. (2013). Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort. Neurogenetics. 14(3-4). 181–188. 26 indexed citations
11.
Goh, Elaine, César P. Canales, Phillip Ruiz, et al.. (2012). Definition of a critical genetic interval related to kidney abnormalities in the Potocki–Lupski syndrome. American Journal of Medical Genetics Part A. 158A(7). 1579–1588. 7 indexed citations
12.
Bourassa, Cynthia V., Inge A. Meijer, Nancy D. Merner, et al.. (2012). VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families. The American Journal of Human Genetics. 91(3). 548–552. 32 indexed citations
13.
Bigio, Marc R. Del, Albert E. Chudley, Harvey B. Sarnat, et al.. (2010). Infantile muscular dystrophy in Canadian aboriginals is an αB‐crystallinopathy. Annals of Neurology. 69(5). 866–871. 41 indexed citations
14.
Seemann, Natashia M., Kathryn Selby, Laura McAdam, et al.. (2010). Symptomatic dystrophinopathies in female children. Neuromuscular Disorders. 21(3). 172–177. 21 indexed citations
15.
Goobie, Sharan, Jeroen Knijnenburg, David Fitzpatrick, et al.. (2008). Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. Cytogenetic and Genome Research. 123(1-4). 65–78. 30 indexed citations
16.
Popović, M., Sharan Goobie, Jodi Morrison, et al.. (2002). Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene. European Journal of Human Genetics. 10(4). 250–258. 16 indexed citations
17.
Goobie, Sharan, M. Popović, Jodi Morrison, et al.. (2001). Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7. The American Journal of Human Genetics. 68(4). 1048–1054. 93 indexed citations
18.
Ginzberg, Hedy, Jumi A. Shin, Lynda Ellis, et al.. (2000). Segregation Analysis in Shwachman-Diamond Syndrome: Evidence for Recessive Inheritance. The American Journal of Human Genetics. 66(4). 1413–1416. 32 indexed citations
19.
Goobie, Sharan, Jodi Morrison, Hedy Ginzberg, et al.. (1999). Exclusion of linkage of Shwachman-Diamond syndrome to chromosome regions 6q and 12q implicated by a de novo translocation. American Journal of Medical Genetics. 85(2). 171–174. 11 indexed citations
20.
Goobie, Sharan, et al.. (1998). Genetic Analysis of Familial Myelodysplastic Syndrome. Cancer Genetics and Cytogenetics. 105(2). 113–118. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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