David D. Weaver
Impact in
- Developmental Biology top 1%
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 62
- Genomic variations and chromosomal abnormalities 23
- Genetic Syndromes and Imprinting 10
- Connective tissue disorders research 10
- Craniofacial Disorders and Treatments 10
- Congenital Ear and Nasal Anomalies 9
- Co-authors
- John M. Opitz (12 shared papers)James F. Reynolds (6 shared papers)Jan Nico Bouwes Bavinck (2 shared papers)Catherine G. Palmer (10 shared papers)Marilyn J. Bull (10 shared papers)Gail H. Vance (12 shared papers)Patricia G. Wheeler (8 shared papers)Laura Russell (2 shared papers)
- Journals
- Clinical Genetics (8 papers)Journal of Medical Genetics (4 papers)American Journal of Medical Genetics (33 papers)Birth Defects Research Part A Clinical and Molecular Teratology (3 papers)Human Genetics (3 papers)
- Partner nations
- United StatesCanadaSpain
In The Last Decade
David D. Weaver
117 papers receiving 3.4k citations
David D. Weaver's Hit Papers
Peers
Comparison fields: 5 of 111
- Developmental Biology 208
- Genetics 1.6k
- Urology 232
- Pediatrics, Perinatology and Child Health 656
- Genetics 341
Countries citing papers authored by David D. Weaver
This map shows the geographic impact of David D. Weaver'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 David D. Weaver with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David D. Weaver more than expected).
Fields of papers citing papers by David D. Weaver
This network shows the impact of papers produced by David D. Weaver. 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 David D. Weaver. The network helps show where David D. Weaver may publish in the future.
Co-authors
The 25 scholars most cited alongside David D. Weaver, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 118 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel‐Feil, and Möbius anomalies Hit paper breakdown → | 1986 | 436 |
| 2 | 1986 | 250 | |
| 3 | 2011 | 216 | |
| 4 | 1974 | 141 | |
| 5 | 1981 | 121 | |
| 6 | 2007 | 82 | |
| 7 | 1985 | 81 | |
| 8 | 2008 | 80 | |
| 9 | 1984 | 76 | |
| 10 | 1998 | 65 | |
| 11 | 2015 | 64 | |
| 12 | 1984 | 60 | |
| 13 | 2013 | 59 | |
| 14 | 1985 | 58 | |
| 15 | 2001 | 58 | |
| 16 | Trisomy 7 mosaicism and manifestations of Goldenhar syndrome with unilateral radial hypoplasia. | 1981 | 58 |
| 17 | 1983 | 55 | |
| 18 | 1984 | 51 | |
| 19 | 2019 | 50 | |
| 20 | 2001 | 50 |
About David D. Weaver
David D. Weaver is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Genetics, having authored 118 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (13 papers), Congenital Anomalies and Fetal Surgery (11 papers), Genetic Syndromes and Imprinting (10 papers), Connective tissue disorders research (10 papers), Craniofacial Disorders and Treatments (10 papers), Congenital Ear and Nasal Anomalies (9 papers) and Urological Disorders and Treatments (9 papers). The work is most often cited by research in Developmental Biology (208 citations), Genetics (1.6k citations), Urology (232 citations), Pediatrics, Perinatology and Child Health (656 citations) and Genetics (341 citations). David D. Weaver has collaborated with scholars based in United States, Canada and Spain. Frequent co-authors include John M. Opitz, James F. Reynolds, Jan Nico Bouwes Bavinck, Catherine G. Palmer, Marilyn J. Bull, Gail H. Vance, Patricia G. Wheeler, Laura Russell, Mark J. Pettenati and Rebecca S. Wappner. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, American Journal of Medical Genetics, Birth Defects Research Part A Clinical and Molecular Teratology and Human Genetics.
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.