Standout Papers
- Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas (1989)
- Multicolor Spectral Karyotyping of Human Chromosomes (1996)
- Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats (1993)
- ClinGen — The Clinical Genome Resource (2015)
- Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene (2008)
- Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome (1981)
- Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders (2019)
Immediate Impact
16 by Nobel laureates 72 from Science/Nature 108 standout
Citing Papers
Pharmacogenomics in the clinic
2015 StandoutNature
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
2011 StandoutNature
Works of David H. Ledbetter being referenced
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
2008 Standout
An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture
2000
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| David H. Ledbetter | 13154 | 11874 | 4896 | 332 | 23.7k | |
| Stylianos E. Antonarakis | 13150 | 22035 | 3052 | 593 | 40.5k | |
| Arthur L. Beaudet | 12287 | 17519 | 3135 | 332 | 29.8k | |
| Stephen W. Scherer | 18061 | 22149 | 2641 | 530 | 39.1k | |
| Grant W. Montgomery | 10915 | 7541 | 1465 | 494 | 25.1k | |
| Han G. Brunner | 8953 | 11657 | 1233 | 277 | 20.4k | |
| James R. Lupski | 17403 | 20334 | 2466 | 575 | 36.5k | |
| Uta Francke | 14319 | 23981 | 1967 | 500 | 41.4k | |
| Martin M. Matzuk | 9449 | 24076 | 1653 | 400 | 41.6k | |
| Stanley F. Nelson | 3693 | 10764 | 1299 | 206 | 18.4k | |
| Niels Tommerup | 7400 | 10661 | 1148 | 302 | 16.2k |
All Works
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