Susan Byck

417 total citations
9 papers, 299 citations indexed

About

Susan Byck is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Susan Byck has authored 9 papers receiving a total of 299 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 4 papers in Rheumatology. Recurrent topics in Susan Byck's work include Metabolism and Genetic Disorders (9 papers), Folate and B Vitamins Research (4 papers) and Biochemical and Molecular Research (3 papers). Susan Byck is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Folate and B Vitamins Research (4 papers) and Biochemical and Molecular Research (3 papers). Susan Byck collaborates with scholars based in Canada, United Kingdom and India. Susan Byck's co-authors include Eileen P. Treacy, Charles R. Scriver, Paula J. Waters, Piotr Nowacki, Emre Kayaalp, C. R. Scriver, Linda Tyfield, C Clow, Przemysław Nowacki and C R Scriver and has published in prestigious journals such as Nucleic Acids Research, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Susan Byck

9 papers receiving 294 citations

Peers

Susan Byck

CB

MB

RHEUM

PHYSI

GENET

Rebecca Mardach United States

S.L.C. Woo United States

Morten J. Corydon Denmark

Zhuwen Gong China

Magalie Barth France

J.A.M. Smeitink Netherlands

Ardeshir A. Monavari Ireland

Pilar Quijada‐Fraile Spain

Loreta Cimbalistienė Lithuania

Iria Roca Spain

Rebecca Mardach United States

Susan Byck

164 ×0.6

CB

193 ×1.0

MB

53 ×0.5

RHEUM

100 ×1.7

PHYSI

40 ×0.9

GENET

Citations per year, relative to Susan Byck Susan Byck (= 1×) peers Rebecca Mardach

Countries citing papers authored by Susan Byck

Since Specialization

Citations

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

Fields of papers citing papers by Susan Byck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Byck

This figure shows the co-authorship network connecting the top 25 collaborators of Susan Byck. A scholar is included among the top collaborators of Susan Byck 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 Susan Byck. Susan Byck is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Scriver, Charles R., et al.. (2007). The Phenylalanine Hydroxylase Locus: A Marker for the History of Phenylketonuria and Human Genetic Diversity. Novartis Foundation symposium. 197. 73–96. 9 indexed citations

2.

Byck, Susan, Paula J. Waters, Brent Richards, et al.. (1998). Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experience. European Journal of Human Genetics. 6(1). 61–70. 23 indexed citations

3.

Kayaalp, Emre, Eileen P. Treacy, Paula J. Waters, et al.. (1997). Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations. The American Journal of Human Genetics. 61(6). 1309–1317. 154 indexed citations

4.

Byck, Susan, et al.. (1997). Prediction of multiple hypermutable codons in the human PAH gene: Codon 280 contains recurrent mutations in Quebec and other populations. Human Mutation. 9(4). 316–321. 13 indexed citations

5.

Nowacki, Przemysław, et al.. (1997). The PAH mutation analysis consortium database: update 1996. Nucleic Acids Research. 25(1). 139–142. 29 indexed citations

6.

Byck, Susan, et al.. (1997). Prediction of multiple hypermutable codons in the human PAH gene: Codon 280 contains recurrent mutations in Quebec and other populations. Human Mutation. 9(4). 316–321. 3 indexed citations

7.

Byck, Susan, Ken H. Morgan, Linda Tyfield, Bernd Dworniczak, & C R Scriver. (1994). Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations. Human Molecular Genetics. 3(9). 1675–1677. 28 indexed citations

8.

Treacy, Eileen P., Susan Byck, C Clow, & C. R. Scriver. (1993). 'Celtic' Phenylketonuria Chromosomes Found? Evidence in Two Regions of Quebec Province. European Journal of Human Genetics. 1(3). 220–228. 34 indexed citations

9.

Byck, Susan, et al.. (1991). Metabolic cooperation among cell lines from patients with inborn errors of vitamin B12 metabolism: differential response of cblC and cblD.. PubMed. 14(2). 153–9. 6 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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