Sarah Dyack

2.6k total citations
37 papers, 1.2k citations indexed

About

Sarah Dyack is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sarah Dyack has authored 37 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sarah Dyack's work include Lysosomal Storage Disorders Research (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Metabolism and Genetic Disorders (6 papers). Sarah Dyack is often cited by papers focused on Lysosomal Storage Disorders Research (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Metabolism and Genetic Disorders (6 papers). Sarah Dyack collaborates with scholars based in Canada, United States and United Kingdom. Sarah Dyack's co-authors include Andrea L. Rideout, Pratibha Singhi, Reinaldo Teixeira Ribeiro, W.K. Chong, Kevin Gordon, Shahnaz Ibrahim, Shamshad Gulab, Ron A. Wevers, Maha S. Zaki and Victoria Price and has published in prestigious journals such as The Lancet, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Sarah Dyack

37 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sarah Dyack Canada 15 440 319 214 173 161 37 1.2k
Andrea L. Rideout Canada 12 285 0.6× 230 0.7× 206 1.0× 59 0.3× 45 0.3× 22 830
Virginia K. Proud United States 17 549 1.2× 320 1.0× 184 0.9× 52 0.3× 117 0.7× 32 1.1k
Kanji Yamamoto Japan 17 480 1.1× 125 0.4× 472 2.2× 66 0.4× 91 0.6× 51 1.3k
Luigia De Falco Italy 19 412 0.9× 70 0.2× 241 1.1× 68 0.4× 240 1.5× 43 1.2k
Andrea Mignarri Italy 17 354 0.8× 65 0.2× 216 1.0× 31 0.2× 67 0.4× 38 948
Jozef Hertecant United Arab Emirates 19 498 1.1× 210 0.7× 50 0.2× 54 0.3× 157 1.0× 50 995
Lorena Travaglini Italy 21 1.2k 2.6× 299 0.9× 75 0.4× 23 0.1× 98 0.6× 54 1.7k
J. Lafond Canada 22 424 1.0× 99 0.3× 147 0.7× 65 0.4× 66 0.4× 50 1.2k
Callum Wilson New Zealand 21 956 2.2× 241 0.8× 96 0.4× 19 0.1× 293 1.8× 58 1.6k
Marta Nowik Switzerland 12 454 1.0× 111 0.3× 110 0.5× 143 0.8× 93 0.6× 18 839

Countries citing papers authored by Sarah Dyack

Since Specialization
Citations

This map shows the geographic impact of Sarah Dyack'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 Sarah Dyack with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Dyack more than expected).

Fields of papers citing papers by Sarah Dyack

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah Dyack. 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 Sarah Dyack. The network helps show where Sarah Dyack may publish in the future.

Co-authorship network of co-authors of Sarah Dyack

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Dyack. A scholar is included among the top collaborators of Sarah Dyack 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 Sarah Dyack. Sarah Dyack 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.
Arts, Heleen H., et al.. (2022). Increased intracranial pressure in a patient with Congenital Heart Defect and Ectodermal Dysplasia (CHDED): Extension of phenotype and review of literature. American Journal of Medical Genetics Part A. 191(2). 554–558. 2 indexed citations
2.
Kernohan, Kristin D., Arran McBride, Taila Hartley, et al.. (2019). p21 protein‐activated kinase 1 is associated with severe regressive autism, and epilepsy. Clinical Genetics. 96(5). 449–455. 15 indexed citations
3.
Bjoraker, Kendra, Michael A. Swanson, Curtis R. Coughlin, et al.. (2016). Neurodevelopmental Outcome and Treatment Efficacy of Benzoate and Dextromethorphan in Siblings with Attenuated Nonketotic Hyperglycinemia. The Journal of Pediatrics. 170. 234–239. 47 indexed citations
4.
Auray‐Blais, Christiane, Uma Ramaswami, Michel Boutin, et al.. (2014). Urinary biomarker investigation in children with Fabry disease using tandem mass spectrometry. Clinica Chimica Acta. 438. 195–204. 59 indexed citations
5.
Guo, Dongchuan, Ellen S. Regalado, Darren E. Casteel, et al.. (2013). Recurrent Gain-of-Function Mutation in PRKG1 Causes Thoracic Aortic Aneurysms and Acute Aortic Dissections. The American Journal of Human Genetics. 93(2). 398–404. 162 indexed citations
6.
Tuschl, Karin, Peter T. Clayton, Sídney M. Gospe, et al.. (2012). Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10 , a Manganese Transporter in Man. The American Journal of Human Genetics. 90(3). 457–466. 257 indexed citations
7.
Prasad, Chitra, Kathy N. Speechley, Sarah Dyack, et al.. (2012). Incidence of medium-chain acyl-CoA dehydrogenase deficiency in Canada using the Canadian Paediatric Surveillance Program: Role of newborn screening. Paediatrics & Child Health. 17(4). 185–189. 6 indexed citations
8.
Brock, Jo‐Ann, et al.. (2012). Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: Case report and review of literature. American Journal of Medical Genetics Part A. 158A(2). 406–411. 12 indexed citations
9.
Carter, Melissa T., Sarah Dyack, & Julie Richer. (2010). Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1–q26.3. Clinical Dysmorphology. 19(3). 140–145. 12 indexed citations
10.
Alliman, Sarah, Justine Coppinger, Janet Marcadier, et al.. (2010). Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2. Clinical Genetics. 78(2). 162–168. 20 indexed citations
11.
Guernsey, Duane L., Haiyan Jiang, Dean R. Campagna, et al.. (2009). Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nature Genetics. 41(6). 651–653. 181 indexed citations
12.
Dyack, Sarah, et al.. (2007). An autosomal recessive form of Alagille-like syndrome that is not linked to JAG1. Genetics in Medicine. 9(8). 544–550. 5 indexed citations
13.
Renault, Nisa, Sarah Dyack, Melanie J. Dobson, et al.. (2007). Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females. European Journal of Human Genetics. 15(6). 628–637. 61 indexed citations
14.
Dyack, Sarah, et al.. (2006). Fabry disease and nephrogenic diabetes insipidus. Pediatric Nephrology. 21(8). 1185–1188. 7 indexed citations
15.
Bartsch, Oliver, Alicia Delicado, Sarah Dyack, et al.. (2006). Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome. Human Genetics. 120(2). 179–186. 32 indexed citations
16.
Conway, Jennifer, Sarah Dyack, Bruce Crooks, & Conrad V. Fernandez. (2005). Mixed Donor Chimerism and Low Level Iduronidase Expression May be Adequate for Neurodevelopmental Protection in Hurler Syndrome. The Journal of Pediatrics. 147(1). 106–108. 6 indexed citations
17.
Sylvius, Nicolas, Zofia T. Bilińska, John P. Veinot, et al.. (2005). In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients. Journal of Medical Genetics. 42(8). 639–647. 81 indexed citations
18.
Dyack, Sarah. (2004). Expanded newborn screening: Lessons learned from MCAD deficiency. Paediatrics & Child Health. 9(4). 241–243. 6 indexed citations
19.
West, Michael L., et al.. (2002). A Nova Scotia kindred with Fabry disease. Acta Paediatrica. 91(s439). 116–116. 4 indexed citations
20.
Winsor, E.J.T., et al.. (1999). Risk of false-positive prenatal diagnosis using interphase FISH testing: hybridization of alpha-satellite X probe to chromosome 19. Prenatal Diagnosis. 19(9). 832–836. 11 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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