Sandra Youngman
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
- Neurology top 1%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
Papers in
-
- Genetic Neurodegenerative Diseases 15
-
- CRISPR and Genetic Engineering 6
- DNA Repair Mechanisms 5
- Mitochondrial Function and Pathology 2
- Photosynthetic Processes and Mechanisms 1
- Biochemical and Molecular Research 1
- Co-authors
- Peter S. Harper (11 shared papers)John J. Wasmuth (8 shared papers)James F. Gusella (9 shared papers)Oliver William Quarrell (7 shared papers)Marcy E. MacDonald (6 shared papers)William L. Whaley (4 shared papers)Hans R. Lehrach (5 shared papers)Duncan J. Shaw (4 shared papers)
- Journals
- Journal of Medical Genetics (3 papers)Genomics (3 papers)Human Genetics (1 paper)Neuron (1 paper)Cell (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Sandra Youngman
18 papers receiving 3.4k citations
Sandra Youngman's Hit Papers
Peers
Comparison fields: 5 of 97
- Cellular and Molecular Neuroscience 2.8k
- Neurology 1.1k
- Molecular Biology 2.5k
- Aging 51
- Genetics 484
Countries citing papers authored by Sandra Youngman
This map shows the geographic impact of Sandra 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 Sandra Youngman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Youngman more than expected).
Fields of papers citing papers by Sandra Youngman
This network shows the impact of papers produced by Sandra 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 Sandra Youngman. The network helps show where Sandra Youngman may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Youngman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Hit paper breakdown → | 1993 | 2879 |
| 2 | 1989 | 84 | |
| 3 | 1989 | 73 | |
| 4 | 1990 | 73 | |
| 5 | Defined physical limits of the Huntington disease gene candidate region. | 1991 | 64 |
| 6 | 1987 | 60 | |
| 7 | A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene. | 1990 | 55 |
| 8 | 1991 | 43 | |
| 9 | Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90. | 1989 | 42 |
| 10 | 1996 | 38 | |
| 11 | 1989 | 28 | |
| 12 | 1992 | 28 | |
| 13 | 1985 | 25 | |
| 14 | 1986 | 24 | |
| 15 | 1988 | 19 | |
| 16 | 1988 | 14 | |
| 17 | 1988 | 7 | |
| 18 | 1988 | 1 |
About Sandra Youngman
Sandra Youngman is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Rheumatology and Neurology, having authored 18 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (15 papers), CRISPR and Genetic Engineering (6 papers), DNA Repair Mechanisms (5 papers), Mitochondrial Function and Pathology (2 papers), Photosynthetic Processes and Mechanisms (1 paper), Neurological disorders and treatments (1 paper), Biochemical and Molecular Research (1 paper) and Cystic Fibrosis Research Advances (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (2.8k citations), Neurology (1.1k citations), Molecular Biology (2.5k citations), Aging (51 citations) and Genetics (484 citations). Sandra Youngman has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Peter S. Harper, John J. Wasmuth, James F. Gusella, Oliver William Quarrell, Marcy E. MacDonald, William L. Whaley, Hans R. Lehrach, Duncan J. Shaw, Sarah Baxendale and Gillian P. Bates. Their work appears in journals such as Journal of Medical Genetics, Genomics, Human Genetics, Neuron and Cell.
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.