S Youngman

3.8k total citations
16 papers, 577 citations indexed

About

S Youngman is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, S Youngman has authored 16 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 1 paper in Neurology. Recurrent topics in S Youngman's work include Genetic Neurodegenerative Diseases (13 papers), CRISPR and Genetic Engineering (6 papers) and DNA Repair Mechanisms (5 papers). S Youngman is often cited by papers focused on Genetic Neurodegenerative Diseases (13 papers), CRISPR and Genetic Engineering (6 papers) and DNA Repair Mechanisms (5 papers). S Youngman collaborates with scholars based in United Kingdom, United States and Singapore. S Youngman's co-authors include Peter S. Harper, John J. Wasmuth, James F. Gusella, Oliver Quarrell, Marcy E. MacDonald, William L. Whaley, Duncan J. Shaw, Hans Lehrach, Gillian P. Bates and Sarah Baxendale and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Neuron.

In The Last Decade

S Youngman

16 papers receiving 560 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S Youngman United Kingdom	14	424	348	201	89	83	16	577
Catherine T. Falk United States	12	129 0.3×	157 0.5×	189 0.9×	30 0.3×	168 2.0×	33	495
M. Hoff United States	12	210 0.5×	104 0.3×	253 1.3×	47 0.5×	23 0.3×	39	493
Tetsushi Yamagata Japan	12	448 1.1×	221 0.6×	276 1.4×	69 0.8×	27 0.3×	14	736
Yoshiro Shibasaki United Kingdom	9	254 0.6×	52 0.1×	233 1.2×	39 0.4×	51 0.6×	26	497
X.Y. Hauge United States	7	205 0.5×	106 0.3×	161 0.8×	39 0.4×	25 0.3×	7	417
Shino Shimada Japan	15	315 0.7×	68 0.2×	318 1.6×	45 0.5×	19 0.2×	36	545
Ulrike Thies Germany	10	258 0.6×	141 0.4×	126 0.6×	16 0.2×	67 0.8×	19	357
Naohiro Kurotaki Japan	12	223 0.5×	67 0.2×	312 1.6×	59 0.7×	32 0.4×	20	446
Wout H. Deelen Netherlands	11	232 0.5×	41 0.1×	256 1.3×	12 0.1×	46 0.6×	16	413
Tatsushi Toda Japan	10	268 0.6×	115 0.3×	100 0.5×	16 0.2×	39 0.5×	29	382

Countries citing papers authored by S Youngman

Since Specialization

Citations

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

Fields of papers citing papers by S Youngman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Youngman

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

All Works

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16 of 16 papers shown

Youngman, S, Henri G.A.M. van Luenen, & Ronald H.A. Plasterk. (1996). Rte‐1, a retrotransposon‐like element in Caenorhabditis elegans. FEBS Letters. 380(1-2). 1–7. 41 indexed citations

Youngman, S, Gillian P. Bates, Andrea I. McClatchey, et al.. (1992). The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p. Genomics. 14(2). 350–356. 28 indexed citations

Whaley, William L., Gillian P. Bates, Andrea Novelletto, et al.. (1991). Mapping of cosmid clones in Huntington's disease region of chromosome 4. Somatic Cell and Molecular Genetics. 17(1). 83–91. 40 indexed citations

Bates, Gillian P., Marcy E. MacDonald, Sarah Baxendale, et al.. (1991). Defined physical limits of the Huntington disease gene candidate region.. PubMed. 49(1). 7–16. 59 indexed citations

Bates, Gillian P., Marcy E. MacDonald, Sarah Baxendale, et al.. (1990). A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.. PubMed. 46(4). 762–75. 56 indexed citations

MacDonald, Marcy E., Jonathan L. Haines, Michael Zimmer, et al.. (1989). Recombination events suggest potential sites for the Huntington's disease gene. Neuron. 3(2). 183–190. 79 indexed citations

Youngman, S, Mansoor Sarfarazi, Maja Bućan, et al.. (1989). A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene. Genomics. 5(4). 802–809. 25 indexed citations

Snell, Russell G., L. Lazarou, S Youngman, et al.. (1989). Linkage disequilibrium in Huntington's disease: an improved localisation for the gene.. Journal of Medical Genetics. 26(11). 673–675. 70 indexed citations

Robbins, Carolyn, Jane Theilmann, S Youngman, et al.. (1989). Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.. PubMed. 44(3). 422–5. 40 indexed citations

10.

Harper, Peter S., Oliver Quarrell, & S Youngman. (1988). Huntington's disease: prediction and prevention. Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 319(1194). 285–298. 6 indexed citations

11.

Youngman, S, Duncan J. Shaw, James F. Gusella, et al.. (1988). A DNA probe, D5 [D4S90] mapping to human chromosome 4p16.3. Nucleic Acids Research. 16(4). 1648–1648. 17 indexed citations

12.

Quarrell, Oliver, Audrey Tyler, Meena Upadhyaya, et al.. (1988). Exclusion Testing for Huntingtonʼs Disease in Pregnancy with a Closely Linked DNA Marker. Obstetrical & Gynecological Survey. 43(1). 45–46. 1 indexed citations

13.

Quarrell, Oliver, S Youngman, M. Sarfarazi, & Peter S. Harper. (1988). Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8).. Journal of Medical Genetics. 25(3). 191–194. 14 indexed citations

14.

Quarrell, Oliver, Audrey Tyler, Meena Upadhyaya, et al.. (1987). EXCLUSION TESTING FOR HUNTINGTON'S DISEASE IN PREGNANCY WITH A CLOSELY LINKED DNA MARKER. The Lancet. 329(8545). 1281–1283. 55 indexed citations

15.

Youngman, S, M. Sarfarazi, Oliver Quarrell, et al.. (1986). Studies of a DNA marker (G8) genetically linked to Huntington disease in British families. Human Genetics. 73(4). 333–339. 23 indexed citations

16.

Harper, Peter S., S Youngman, Mary Anne Anderson, et al.. (1985). Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.. Journal of Medical Genetics. 22(6). 447–450. 23 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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