Sarah Dyack

2.7k citations

37 papers · 1.2k · h-index 15

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Developmental Biology top 10%

Papers in

Molecular Biology 14
- Congenital heart defects research 5
Genetics 10
- Genomic variations and chromosomal abnormalities 6
- Connective tissue disorders research 3

Co-authors: Andrea L. Rideout (5 shared papers)Ron A. Wevers (2 shared papers)Karin Tuschl (2 shared papers)Peter T. Clayton (2 shared papers)Maha S. Zaki (2 shared papers)Shahnaz Ibrahim (2 shared papers)Pratibha Singhi (2 shared papers)Orlando Graziani Póvoas Barsottini (1 shared paper)
Journals: Journal of Medical Genetics (4 papers)The Journal of Pediatrics (2 papers)Clinical Genetics (2 papers)Acta Paediatrica (2 papers)The American Journal of Human Genetics (2 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Sarah Dyack

37 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside Sarah Dyack, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sarah Dyack Line = papers co-authored together Sarah Dyack links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10 , a Manganese Transporter in Man The American Journal of Human Genetics ·Karin Tuschl, Peter T. Clayton, Sídney M. Gospe, Shamshad Gulab, Shahnaz Ibrahim, Pratibha Singhi, Roosy Aulakh, Reinaldo Teixeira Ribeiro, Orlando Graziani Póvoas Barsottini, Maha S. Zaki, (unknown), Sarah Dyack, Victoria Price, Andrea L. Rideout, Kevin Gordon, Ron A. Wevers, W.K. Chong, Philippa B. Mills	2012	260
2	Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia Nature Genetics ·Duane L. Guernsey, Haiyan Jiang, Dean R. Campagna, Susan C. Evans, Meghan Ferguson, Mark D. Kellogg, Mathieu Lachance, Makoto Matsuoka, Mathew Nightingale, Andrea L. Rideout, Louis Saint‐Amant, Paul J. Schmidt, Andrew Orr, Sylvia S. Bottomley, Mark D. Fleming, Mark D. Ludman, Sarah Dyack, Conrad V. Fernandez, Mark Samuels	2009	182
3	Recurrent Gain-of-Function Mutation in PRKG1 Causes Thoracic Aortic Aneurysms and Acute Aortic Dissections The American Journal of Human Genetics ·Dongchuan Guo, Ellen S. Regalado, Darren E. Casteel, Regie Lyn P. Santos‐Cortez, Limin Gong, Jeong Joo Kim, Sarah Dyack, S. Gabrielle Horne, Guijuan Chang, Guillaume Jondeau, Cathérine Boileau, Joseph S. Coselli, Zhenyu Li, Suzanne M. Leal, Jay Shendure, Mark J. Rieder, Michael J. Bamshad, Deborah A. Nickerson, Choel Kim, Dianna M. Milewicz	2013	165
4	In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients Journal of Medical Genetics ·Nicolas Sylvius, Zofia T. Bilińska, John P. Veinot, Anna Fidziańska, Pierrette M. Bolongo, Steven S.S. Poon, Pascal McKeown, Rick A. Davies, K.-I. Chan, Antony Tang, Sarah Dyack, Jacek Grzybowski, (unknown), Heidi M. McBride, Frédérique Tesson	2005	81
5	Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females European Journal of Human Genetics ·Nisa Renault, Sarah Dyack, Melanie J. Dobson, Teresa Costa, Wan L. Lam, Wenda Greer	2007	61
6	Urinary biomarker investigation in children with Fabry disease using tandem mass spectrometry Clinica Chimica Acta ·(unknown), Catherine-Marie Blais, Uma Ramaswami, Michel Boutin, Dominique P. Germain, Sarah Dyack, Olaf A. Bodamer, Guillem Pintos‐Morell, Joe T.R. Clarke, Daniel G. Bichet, David G. Warnock, Lucía Echevarría, Michael L. West, Paméla Lavoie	2014	60
7	Neurodevelopmental Outcome and Treatment Efficacy of Benzoate and Dextromethorphan in Siblings with Attenuated Nonketotic Hyperglycinemia The Journal of Pediatrics ·Kendra Bjoraker, Michael A. Swanson, Curtis R. Coughlin, John Christodoulou, Ee Shien Tan, Mark Fergeson, Sarah Dyack, Ayesha Ahmad, Marisa W. Friederich, Elaine Spector, Geralyn Creadon‐Swindell, Marie Antoinette Hodge, Sommer Gaughan, Casey Burns, Johan L.K. Van Hove	2016	48
8	Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation Journal of Medical Genetics ·Gregory R. Handrigan, David Chitayat, Anath C. Lionel, Maury Pinsk, Andrea K. Vaags, Christian R. Marshall, Sarah Dyack, Luis Escobar, Bridget A. Fernandez, Joseph C. Stegman, Jill A. Rosenfeld, Lisa G. Shaffer, McKinsey L. Goodenberger, Jennelle C. Hodge, Jason E. Cain, Riyana Babul‐Hirji, Dimitri J. Stavropoulos, Verna Yiu, Stephen W. Scherer, Norman D. Rosenblum	2013	37
9	SMAD3 pathogenic variants: risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium Journal of Medical Genetics ·(unknown), Ellen S. Regalado, Dongchuan Guo, Nadine Hanna, Pauline Arnaud, Laura Muiño Mosquera, Bert Callewaert, Kwanghyuk Lee, Suzanne M. Leal, Stephanie E Wallace, Andrea L. Rideout, Sarah Dyack, Rajani Aatre, Cathérine Boileau, Julie De Backer, Guillaume Jondeau, Dianna M. Milewicz	2019	36
10	Phenotypic and molecular characterization of 19q12q13.1 deletions: A report of five patients American Journal of Medical Genetics Part A ·Shimul Chowdhury, Anne M. Bandholz, Sandhya Parkash, Sarah Dyack, Andrea L. Rideout, Kathleen A. Leppig, Heidi Thiese, Patricia G. Wheeler, Marilyn Tsang, Blake C. Ballif, Lisa G. Shaffer, Beth S. Torchia, Jay W. Ellison, Jill A. Rosenfeld	2013	33
11	Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein–Taybi syndrome Human Genetics ·Oliver Bartsch, Sasan Rasi, Alicia Delicado, Sarah Dyack, Luitgard M. Neumann, E Seemanová, Marianne Volleth, Thomas Haaf, Vera M. Kalscheuer	2006	32
12	Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2 Clinical Genetics ·Sarah Alliman, Justine Coppinger, Janet Marcadier, Heidi Thiese, Pamela Brock, Sid John Shafer, Christine A. Weaver, Alexander Asamoah, Kathleen A. Leppig, Sarah Dyack, B. Morash, Roger A. Schultz, BS Torchia, AN Lamb, B.A. Bejjani	2010	20
13	Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG) Journal of Medical Genetics ·Melissa T. Carter, Myriam Srour, Ping-Yee Billie Au, Daniela Buhaş, Sarah Dyack, Alison Eaton, Michal Inbar‐Feigenberg, Heather Howley, Anne Kawamura, M. E. Suzanne Lewis, M. Elizabeth McCready, Tanya N. Nelson, Hilary Vallance	2023	20
14	Newborns with C₈‐acylcarnitine level over the 90th centile have an increased frequency of the common MCAD 985A>G mutation Journal of Inherited Metabolic Disease ·B. Blois, Christie Riddell, Kent Dooley, Sarah Dyack	2002	16
15	p21 protein‐activated kinase 1 is associated with severe regressive autism, and epilepsy Clinical Genetics ·Kristin D. Kernohan, Arran McBride, Taila Hartley, Samantha K. Rojas, David A. Dyment, Kym M. Boycott, Sarah Dyack	2019	15
16	High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinoses JIMD Reports ·Abdulhakim Jilani, Diana Matviychuk, Susan Blasér, Sarah Dyack, Jean Mathieu, Asuri N. Prasad, Chitra Prasad, Lianna Kyriakopoulou, Saadet Mercimek‐Andrews	2019	13
17	Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: Case report and review of literature American Journal of Medical Genetics Part A ·Jo‐Ann Brock, Sarah Dyack, Mark D. Ludman, Nadine Dumas, Michele Gaudet, Barbara Morash	2012	12
18	Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1–q26.3 Clinical Dysmorphology ·Melissa T. Carter, Sarah Dyack, Julie Richer	2010	12
19	Risk of false-positive prenatal diagnosis using interphase FISH testing: hybridization of alpha-satellite X probe to chromosome 19 Prenatal Diagnosis ·E.J.T. Winsor, Sarah Dyack, E. Martha Wood-Burgess, Greg Ryan	1999	11
20	Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Pamela Jarrett, Alexander S. Easton, Kenneth Rockwood, Sarah Dyack, (unknown), Victoria Mok Siu, Seyed M. Mirsattari, Andreu Massot‐Tarrús, M Beis, Nolan D’Souza, Sultan Darvesh	2017	8

About Sarah Dyack

Sarah Dyack is a scholar working on Molecular Biology, Genetics, Physiology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 37 papers that have together received 1.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (7 papers), Metabolism and Genetic Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers), Neonatal Health and Biochemistry (3 papers), Connective tissue disorders research (3 papers), Prenatal Screening and Diagnostics (3 papers) and Folate and B Vitamins Research (2 papers). The work is most often cited by research in Clinical Biochemistry (122 citations), Developmental Biology (31 citations), Hematology (144 citations), Nutrition and Dietetics (199 citations) and Health, Toxicology and Mutagenesis (145 citations). Sarah Dyack has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Andrea L. Rideout, Ron A. Wevers, Karin Tuschl, Peter T. Clayton, Maha S. Zaki, Shahnaz Ibrahim, Pratibha Singhi, Orlando Graziani Póvoas Barsottini, Philippa B. Mills and Kevin Gordon. Their work appears in journals such as Journal of Medical Genetics, The Journal of Pediatrics, Clinical Genetics, Acta Paediatrica and The American Journal of Human Genetics.

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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Sarah Dyack

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Sarah Dyack

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