Widukind Lenz
Widukind Lenz publishes mostly in Genetics, Developmental Biology and Molecular Biology, on topics such as Congenital limb and hand anomalies, Medical and Biological Sciences and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities.
- World rank
- #585,907 of 7,710,434 ranked researchers
- Rank in Germany
- #28,824 of 364,343
- Works
- 151
- Citations
- 4.8k
- Citations per work
- 31.7
What does Widukind Lenz research?
Widukind Lenz's work is mostly in Biochemistry, Genetics and Molecular Biology (38%), Medicine (18%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Everything else6643.9%
- Life Sciences5838.3%
- Health Sciences2717.8%
- Medicine2717.8%
- 1Genetics20% of their works
- 2Developmental Biology10% of their works
- 3Molecular Biology9% of their works
- 4Pediatrics, Perinatology and Child Health8% of their works
- 5Surgery6% of their works
- 6Hematology4% of their works
Research topics
- Congenital limb and hand anomalies
- Medical and Biological Sciences
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Bone fractures and treatments
- Prenatal Screening and Diagnostics
- Congenital Anomalies and Fetal Surgery
- Sexual Differentiation and Disorders
Which keywords describe Widukind Lenz's research?
The keywords of their largest research topics: Epidemiology, Genetic Heterogeneity, Limb Malformations, Prenatal Diagnosis, Anatomical Nomenclature, Eponyms, Sex Determination and X Chromosome Inactivation.
- Steroid 21-Hydroxylase Deficiency
- Omphalocele
- Marfan Syndrome
- Fracture Epidemiology
- Bone Healing
- X Chromosome Inactivation
- Eponyms
- Prenatal Diagnosis
- Genetic Heterogeneity
- Epidemiology
- Limb Malformations
- Anatomical Nomenclature
- Sex Determination
- Aneuploidy Screening
- Ehlers-Danlos Syndrome
- Gastroschisis
- Maternal Plasma DNA Sequencing
- Congenital Adrenal Hyperplasia
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most.
All 18 words, with their numbers
- Epidemiology402 topics
- Genetic Heterogeneity321 topic
- Limb Malformations321 topic
- Prenatal Diagnosis162 topics
- Anatomical Nomenclature121 topic
- Eponyms121 topic
- Sex Determination91 topic
- X Chromosome Inactivation91 topic
- Aneuploidy Screening81 topic
- Bone Healing81 topic
- Ehlers-Danlos Syndrome81 topic
- Fracture Epidemiology81 topic
- Gastroschisis81 topic
- Marfan Syndrome81 topic
- Maternal Plasma DNA Sequencing81 topic
- Omphalocele81 topic
- Congenital Adrenal Hyperplasia71 topic
- Steroid 21-Hydroxylase Deficiency71 topic
Where does Widukind Lenz work?
Widukind Lenz's main affiliation in the publication record is University of Münster, Germany.
How many publications and citations does Widukind Lenz have?
OpenAlex counts 151 works and 4,793 citations for Widukind Lenz, an h-index of 33, ranking #585,907 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
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