S Youngman

3.8k citations

16 papers · 577 indexed · h-index 14

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Cellular and Molecular Neuroscience 13
- Genetic Neurodegenerative Diseases 13
Molecular Biology 11
- CRISPR and Genetic Engineering 6
- DNA Repair Mechanisms 5
- Mitochondrial Function and Pathology 2
- Biochemical and Molecular Research 1
- RNA and protein synthesis mechanisms 1

Co-authors: Peter S. Harper (11 shared papers)John J. Wasmuth (8 shared papers)James F. Gusella (9 shared papers)Oliver Quarrell (7 shared papers)Marcy E. MacDonald (6 shared papers)William L. Whaley (4 shared papers)Duncan J. Shaw (4 shared papers)Hans Lehrach (5 shared papers)
Journals: Journal of Medical Genetics (3 papers)Genomics (2 papers)FEBS Letters (1 paper)The Lancet (1 paper)Neuron (1 paper)
Partner nations: United Kingdom United States South Africa

In The Last Decade

S Youngman

16 papers receiving 560 citations

Peers

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-authors

The 25 scholars most cited alongside S Youngman, 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 S Youngman Line = papers co-authored together S Youngman links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

#	Work
1	Recombination events suggest potential sites for the Huntington's disease gene Neuron ·Marcy E. MacDonald, Jonathan L. Haines, Michael Zimmer, Shirley V. Cheng, S Youngman, William L. Whaley, Nancy S. Wexler, Maja Bućan, Bernice A. Allitto, Barbara A. Smith, Julie Leavitt, Annemarie Poustka, Peter S. Harper, Hans Lehrach, John J. Wasmuth, Anna-Marie Frischauf, James F. Gusella	1989	79
2	Linkage disequilibrium in Huntington's disease: an improved localisation for the gene. Journal of Medical Genetics ·Russell G. Snell, L. Lazarou, S Youngman, Oliver Quarrell, John J. Wasmuth, Duncan J. Shaw, Peter S. Harper	1989	70
3	Defined physical limits of the Huntington disease gene candidate region. PubMed ·Gillian P. Bates, Marcy E. MacDonald, Sarah Baxendale, S Youngman, Carol Sze Ki Lin, William L. Whaley, John J. Wasmuth, James F. Gusella, Hans Lehrach	1991	59
4	A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene. PubMed ·Gillian P. Bates, Marcy E. MacDonald, Sarah Baxendale, Zdeněk Sedláček, S Youngman, Donna Romano, William L. Whaley, Bernice A. Allitto, Annemarie Poustka, James F. Gusella	1990	56
5	EXCLUSION TESTING FOR HUNTINGTON'S DISEASE IN PREGNANCY WITH A CLOSELY LINKED DNA MARKER The Lancet ·Oliver Quarrell, Audrey Tyler, Meena Upadhyaya, Andrea L. Meredith, S Youngman, Peter S. Harper	1987	55
6	Rte‐1, a retrotransposon‐like element in Caenorhabditis elegans FEBS Letters ·S Youngman, Henri G.A.M. van Luenen, Ronald H.A. Plasterk	1996	41
7	Mapping of cosmid clones in Huntington's disease region of chromosome 4 Somatic Cell and Molecular Genetics ·William L. Whaley, Gillian P. Bates, Andrea Novelletto, Zdeněk Sedláček, Shirley V. Cheng, Donna Romano, Elizabeth Ormondroyd, Bernice A. Allitto, Carol Sze Ki Lin, S Youngman, Sarah Baxendale, Maja Bućan, Michael R. Altherr, John J. Wasmuth, Nancy S. Wexler, Marina Frontali, Annemarie Frischauf, Hans Lehrach, Marcy E. MacDonald, James F. Gusella	1991	40
8	Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90. PubMed ·Carolyn Robbins, Jane Theilmann, S Youngman, Jonathan L. Haines, M J Altherr, Peter S. Harper, Carolyn Payne, Anne Junker, John J. Wasmuth, Michael R. Hayden	1989	40
9	The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p Genomics ·S Youngman, Gillian P. Bates, Sarah Williams, Andrea I. McClatchey, Sarah Baxendale, Zdeněk Sedláček, Michael R. Altherr, John J. Wasmuth, Marcy E. MacDonald, James F. Gusella, Denise Sheer, Hans Lehrach	1992	28
10	A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene Genomics ·S Youngman, Mansoor Sarfarazi, Maja Bućan, Marcy E. MacDonald, Barbara A. Smith, Michael Zimmer, Conrad Gilliam, Anna‐Maria Frischauf, John J. Wasmuth, James F. Gusella, Hans Lehrach, Peter S. Harper, Duncan J. Shaw	1989	25
11	Studies of a DNA marker (G8) genetically linked to Huntington disease in British families Human Genetics ·S Youngman, M. Sarfarazi, Oliver Quarrell, P. M. Conneally, Karen Gibbons, Peter S. Harper, Duncan J. Shaw, Rudolph E. Tanzi, Margaret R. Wallace, James F. Gusella	1986	23
12	Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families. Journal of Medical Genetics ·Peter S. Harper, S Youngman, Mary Anne Anderson, M. Sarfarazi, Oliver Quarrell, Rudolph E. Tanzi, Duncan Shaw, Patricia G. Wallace, P.M. Conneally, James F. Gusella	1985	23
13	A DNA probe, D5 [D4S90] mapping to human chromosome 4p16.3 Nucleic Acids Research ·S Youngman, Duncan J. Shaw, James F. Gusella, Marcy E. MacDonald, Eric J. Stanbridge, John J. Wasmuth, Peter S. Harper	1988	17
14	Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8). Journal of Medical Genetics ·Oliver Quarrell, S Youngman, M. Sarfarazi, Peter S. Harper	1988	14
15	Huntington's disease: prediction and prevention Philosophical transactions of the Royal Society of London. Series B, Biological sciences ·Peter S. Harper, Oliver Quarrell, S Youngman	1988	6
16	Exclusion Testing for Huntingtonʼs Disease in Pregnancy with a Closely Linked DNA Marker Obstetrical & Gynecological Survey ·Oliver Quarrell, Audrey Tyler, Meena Upadhyaya, Andrea L. Meredith, S Youngman, Peter S. Harper	1988	1

About S Youngman

S Youngman is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Pulmonary and Respiratory Medicine and Rheumatology, having authored 16 papers that have together received 577 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (13 papers), CRISPR and Genetic Engineering (6 papers), DNA Repair Mechanisms (5 papers), Mitochondrial Function and Pathology (2 papers), Cystic Fibrosis Research Advances (1 paper), Plant nutrient uptake and metabolism (1 paper), Biochemical and Molecular Research (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (348 citations), Genetics (201 citations), Molecular Biology (424 citations), Neurology (83 citations) and Aging (5 citations). S Youngman has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent 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, Sarah Baxendale and Gillian P. Bates. Their work appears in journals such as Journal of Medical Genetics, Genomics, FEBS Letters, The Lancet and Neuron.

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.

Explore authors with similar magnitude of impact