Opitz Jm
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Cleft Lip and Palate Research
Papers in
- Co-authors
- Gilbert Ef (10 shared papers)Jens Herrmann (2 shared papers)J. Herrmann (4 shared papers)Klaus Pätau (1 shared paper)Leonard Freedman (1 shared paper)Judith G. Hall (1 shared paper)B. Rafael Elejalde (1 shared paper)Enid Gilbert‐Barness (1 shared paper)
- Journals
- Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) (3 papers)PubMed (31 papers)
- Partner nations
- United StatesThailand
In The Last Decade
Opitz Jm
33 papers receiving 547 citations
Peers
Comparison fields: 5 of 71
- Developmental Biology 50
- Genetics 317
- Urology 58
- Pediatrics, Perinatology and Child Health 159
- Medical Terminology 1
Countries citing papers authored by Opitz Jm
This map shows the geographic impact of Opitz Jm'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 Opitz Jm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Opitz Jm more than expected).
Fields of papers citing papers by Opitz Jm
This network shows the impact of papers produced by Opitz Jm. 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 Opitz Jm. The network helps show where Opitz Jm may publish in the future.
Co-authors
The 18 scholars most cited alongside Opitz Jm, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies. | 1975 | 102 |
| 2 | Blastogenesis and the "primary field" in human development. | 1993 | 99 |
| 3 | Developmental and other pathologic changes in syndromes caused by chromosome abnormalities. | 1982 | 46 |
| 4 | Diagnostic/genetic studies in severe mental retardation. | 1978 | 38 |
| 5 | An application of numerical taxonomy to the classification of syndromes. | 1977 | 30 |
| 6 | Anatomic studies in the 18-trisomy syndrome. | 1970 | 25 |
| 7 | Studies of malformation syndromes in man XXXXII: a pleiotropic dominant mutation affecting skeletal, sexual and apocrine-mammary development. | 1976 | 23 |
| 8 | A partial trisomy 5p syndrome. | 1975 | 23 |
| 9 | Naming and nomenclature of syndromes. | 1974 | 20 |
| 10 | Pathogenetic analysis of congenital anomalies in humans. | 1982 | 19 |
| 11 | Pathogenetic analysis of certain developmental and genetic ectodermal defects. | 1988 | 18 |
| 12 | The pathology of some malformations and hereditary diseases of the respiratory tract. | 1976 | 17 |
| 13 | Developmental abnormalities resulting in short umbilical cord. | 1993 | 13 |
| 14 | Follow-up on a human X-autosome translocation first studied in 1963 and 1964. | 1978 | 13 |
| 15 | The developmental field concept in pediatric pathology--especially with respect to fibular a/hypoplasia and the DiGeorge anomaly. | 1987 | 12 |
| 16 | Growth analysis in clinical genetics. | 1985 | 12 |
| 17 | Arthrodentoosteodysplasia: a genetic "acroosteolysis" syndrome. | 1974 | 9 |
| 18 | Grebe chondrodysplasia and similar forms of severe short-limbed dwarfism. | 1977 | 7 |
| 19 | Study of a child with an "idiopathic" malformation/mental retardation syndrome. | 1975 | 7 |
| 20 | The developmental analysis of human congenital anomalies. | 1982 | 7 |
About Opitz Jm
Opitz Jm is a scholar working on Genetics, Surgery, Pediatrics, Perinatology and Child Health, Molecular Biology and Developmental Biology, having authored 34 papers that have together received 594 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Congenital Anomalies and Fetal Surgery (3 papers), Connective tissue disorders research (2 papers), Congenital Diaphragmatic Hernia Studies (2 papers), Congenital limb and hand anomalies (2 papers), Medical and Biological Sciences (2 papers) and Pancreatic function and diabetes (1 paper). The work is most often cited by research in Developmental Biology (50 citations), Genetics (317 citations), Urology (58 citations), Pediatrics, Perinatology and Child Health (159 citations) and Medical Terminology (1 citation). Opitz Jm has collaborated with scholars based in United States and Thailand. Frequent co-authors include Gilbert Ef, Jens Herrmann, J. Herrmann, Klaus Pätau, Leonard Freedman, Judith G. Hall, B. Rafael Elejalde, Enid Gilbert‐Barness, Chirane Viseskul and Murray Feingold. Their work appears in journals such as Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) and PubMed.
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.