W. Hammans
Impact in
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Fetal and Pediatric Neurological Disorders
-
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
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- Prenatal Screening and Diagnostics 11
- Genetics 9
- Genomic variations and chromosomal abnormalities 7
- Genetic Syndromes and Imprinting 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- B. Eiben (14 shared papers)R. Goebel (10 shared papers)Martha Hentemann (1 shared paper)R. Osmers (1 shared paper)Iris Bartels (1 shared paper)Jörg T. Epplen (5 shared papers)Susanne Hansen (4 shared papers)M. Pruggmayer (1 shared paper)
- Journals
- Prenatal Diagnosis (5 papers)Fetal Diagnosis and Therapy (2 papers)Human Genetics (2 papers)Geburtshilfe und Frauenheilkunde (3 papers)DMW - Deutsche Medizinische Wochenschrift (2 papers)
- Partner nations
- Germany
In The Last Decade
W. Hammans
15 papers receiving 361 citations
Peers
Comparison fields: 5 of 41
- Pediatrics, Perinatology and Child Health 297
- Genetics 161
- Developmental Biology 6
- Public Health, Environmental and Occupational Health 63
- Obstetrics and Gynecology 14
Countries citing papers authored by W. Hammans
This map shows the geographic impact of W. Hammans'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 W. Hammans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. Hammans more than expected).
Fields of papers citing papers by W. Hammans
This network shows the impact of papers produced by W. Hammans. 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 W. Hammans. The network helps show where W. Hammans may publish in the future.
Co-authors
The 16 scholars most cited alongside W. Hammans, 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 | Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage. | 1990 | 228 |
| 2 | 1999 | 62 | |
| 3 | 1994 | 30 | |
| 4 | 1998 | 29 | |
| 5 | 1989 | 13 | |
| 6 | 1992 | 10 | |
| 7 | 1989 | 9 | |
| 8 | 1993 | 5 | |
| 9 | 2009 | 3 | |
| 10 | 1998 | 3 | |
| 11 | 2001 | 2 | |
| 12 | 1992 | 1 | |
| 13 | 2008 | 1 | |
| 14 | 1988 | 1 | |
| 15 | [On the urgency of the early diagnosis of carcinoma of the uterine cervix during pregnancy (author's transl)]. | 1973 | 1 |
| 16 | [Paresis of the femoral nerve following vaginal hysterectomy and its medico-legal implication (author's transl)]. | 1975 | 1 |
| 17 | 1982 | 0 | |
| 18 | 2000 | 0 |
About W. Hammans
W. Hammans is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Oncology and Molecular Biology, having authored 18 papers that have together received 399 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Congenital Anomalies and Fetal Surgery (5 papers), Genetic Syndromes and Imprinting (2 papers), Cancer Risks and Factors (2 papers), Chromosomal and Genetic Variations (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Endometrial and Cervical Cancer Treatments (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (297 citations), Genetics (161 citations), Developmental Biology (6 citations), Public Health, Environmental and Occupational Health (63 citations) and Obstetrics and Gynecology (14 citations). W. Hammans has collaborated with scholars based in Germany. Frequent co-authors include B. Eiben, R. Goebel, Martha Hentemann, R. Osmers, Iris Bartels, Jörg T. Epplen, Susanne Hansen, M. Pruggmayer, Gesa Schwanitz and M. Vogel. Their work appears in journals such as Prenatal Diagnosis, Fetal Diagnosis and Therapy, Human Genetics, Geburtshilfe und Frauenheilkunde and DMW - Deutsche Medizinische Wochenschrift.
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.