LuAnn Weik
Impact in
- Developmental Biology top 10%
- Congenital limb and hand anomalies
-
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Craniofacial Disorders and Treatments
Papers in
-
- Congenital heart defects research 2
- Chromatin Remodeling and Cancer 1
- Hedgehog Signaling Pathway Studies 1
- Genetics 4
- Cleft Lip and Palate Research 1
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Virginia P. Johnson (1 shared paper)Mark Lubinsky (1 shared paper)Amanda Collins (1 shared paper)Yi Duan (1 shared paper)Maximilian Muenke (1 shared paper)Raoul C. M. Hennekam (1 shared paper)Fiorella Gurrieri (1 shared paper)Christiane Bay (1 shared paper)
- Journals
- American Journal of Speech-Language Pathology (1 paper)Journal of Pediatric Genetics (1 paper)Proceedings of the National Academy of Sciences (1 paper)Genes (1 paper)Journal of Thrombosis and Haemostasis (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
LuAnn Weik
7 papers receiving 145 citations
Peers
Comparison fields: 5 of 42
- Developmental Biology 18
- Genetics 99
- Pediatrics, Perinatology and Child Health 35
- Molecular Biology 102
- Anatomy 1
Countries citing papers authored by LuAnn Weik
This map shows the geographic impact of LuAnn Weik'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 LuAnn Weik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites LuAnn Weik more than expected).
Fields of papers citing papers by LuAnn Weik
This network shows the impact of papers produced by LuAnn Weik. 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 LuAnn Weik. The network helps show where LuAnn Weik may publish in the future.
Co-authors
The 25 scholars most cited alongside LuAnn Weik, 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 | 1994 | 97 | |
| 2 | 2009 | 21 | |
| 3 | 1999 | 11 | |
| 4 | 2018 | 10 | |
| 5 | 2022 | 8 | |
| 6 | 2017 | 4 | |
| 7 | Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence. | 2017 | 1 |
About LuAnn Weik
LuAnn Weik is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Pulmonary and Respiratory Medicine, having authored 7 papers that have together received 152 indexed citations. Recurring topics across this work include Congenital heart defects research (2 papers), interferon and immune responses (1 paper), Blood groups and transfusion (1 paper), Chromatin Remodeling and Cancer (1 paper), Cleft Lip and Palate Research (1 paper), Platelet Disorders and Treatments (1 paper), Hedgehog Signaling Pathway Studies (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Developmental Biology (18 citations), Genetics (99 citations), Pediatrics, Perinatology and Child Health (35 citations), Molecular Biology (102 citations) and Anatomy (1 citation). LuAnn Weik has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Virginia P. Johnson, Mark Lubinsky, Amanda Collins, Yi Duan, Maximilian Muenke, Raoul C. M. Hennekam, Fiorella Gurrieri, Christiane Bay, G. Bradley Schaefer and Donald Basel. Their work appears in journals such as American Journal of Speech-Language Pathology, Journal of Pediatric Genetics, Proceedings of the National Academy of Sciences, Genes and Journal of Thrombosis and Haemostasis.
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.