Richard E. Lutz

1.1k total citations
18 papers, 256 citations indexed

About

Richard E. Lutz is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Richard E. Lutz has authored 18 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Oncology. Recurrent topics in Richard E. Lutz's work include Biochemical and Molecular Research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Bone health and treatments (3 papers). Richard E. Lutz is often cited by papers focused on Biochemical and Molecular Research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Bone health and treatments (3 papers). Richard E. Lutz collaborates with scholars based in United States, Australia and Hungary. Richard E. Lutz's co-authors include G. Bradley Schaefer, Deeksha Bali, Jennifer Goldstein, Catherine Rehder, David A. Weinstein, Priya S. Kishnani, Anne Boney, Avihu Boneh, Stephanie Austin and Dean S. Morrell and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bone and Genetics in Medicine.

In The Last Decade

Richard E. Lutz

17 papers receiving 246 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Richard E. Lutz United States 10 139 98 70 48 19 18 256
Raquel Boy Brazil 10 97 0.7× 85 0.9× 30 0.4× 24 0.5× 31 1.6× 25 264
MB Delatycki Australia 10 89 0.6× 37 0.4× 24 0.3× 32 0.7× 12 0.6× 12 377
Elisa Biamino Italy 13 204 1.5× 188 1.9× 29 0.4× 19 0.4× 29 1.5× 25 456
Anne Chun‐Hui Tsai United States 10 117 0.8× 126 1.3× 27 0.4× 58 1.2× 11 0.6× 22 295
Louise Bier United States 9 152 1.1× 90 0.9× 30 0.4× 17 0.4× 44 2.3× 16 485
Heidi Mateus Colombia 11 119 0.9× 165 1.7× 33 0.5× 12 0.3× 45 2.4× 32 362
Noboru Fueki Japan 10 76 0.5× 207 2.1× 24 0.3× 27 0.6× 31 1.6× 24 356
Ngozi A. Nwokoro United States 10 217 1.6× 330 3.4× 74 1.1× 22 0.5× 22 1.2× 13 560
Wakaba Endo Japan 12 108 0.8× 151 1.5× 27 0.4× 22 0.5× 43 2.3× 38 365
Riina Žordania Estonia 12 140 1.0× 182 1.9× 15 0.2× 21 0.4× 7 0.4× 25 350

Countries citing papers authored by Richard E. Lutz

Since Specialization
Citations

This map shows the geographic impact of Richard E. Lutz'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 Richard E. Lutz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard E. Lutz more than expected).

Fields of papers citing papers by Richard E. Lutz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard E. Lutz. 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 Richard E. Lutz. The network helps show where Richard E. Lutz may publish in the future.

Co-authorship network of co-authors of Richard E. Lutz

This figure shows the co-authorship network connecting the top 25 collaborators of Richard E. Lutz. A scholar is included among the top collaborators of Richard E. Lutz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Richard E. Lutz. Richard E. Lutz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
2.
Mariotti, Laura, et al.. (2020). The iron–sulphur cluster in human DNA2 is required for all biochemical activities of DNA2. Communications Biology. 3(1). 322–322. 16 indexed citations
3.
Adegbola, Abidemi, Richard E. Lutz, Elina Nikkola, et al.. (2020). Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia. SHILAP Revista de lepidopterología. 1(1). 100007–100007. 9 indexed citations
4.
Starr, Lois J., Jürgen W. Spranger, Vamshi K. Rao, Richard E. Lutz, & Anji T. Yetman. (2019). PIGQ glycosylphosphatidylinositol‐anchored protein deficiency: Characterizing the phenotype. American Journal of Medical Genetics Part A. 179(7). 1270–1275. 9 indexed citations
5.
Margraf, Rebecca L., Jacob Durtschi, Bryan L. Krock, et al.. (2018). Novel PLP1 Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical Phenotypes. SHILAP Revista de lepidopterología. 5. 2329048X18789282–2329048X18789282. 2 indexed citations
6.
Wang, Jing, Victor Wei Zhang, Tian Xia, et al.. (2015). Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types. Genetics in Medicine. 18(5). 513–521. 21 indexed citations
7.
Lutz, Richard E., et al.. (2015). Osteogenesis imperfecta caused by PPIB mutation with severe phenotype and congenital hearing loss. Journal of Pediatric Genetics. 3(1). 29–34. 3 indexed citations
8.
Bishop, Nicholas, Jill H. Simmons, Richard E. Lutz, et al.. (2014). Hypophosphatasia: Gross Motor Function and Height Improvement in Infants and Young Children Treated with Asfotase Alfa for up to 3 Years. 82. 2 indexed citations
9.
Whyte, Michael P., Jill H. Simmons, Richard E. Lutz, et al.. (2014). Sustained efficacy and tolerability in infants and young children with life-threatening hypophosphatasia treated with asfotase alfa. Bone Abstracts. 5 indexed citations
10.
Bali, Deeksha, Jennifer Goldstein, Catherine Rehder, et al.. (2013). Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene. Molecular Genetics and Metabolism. 111(3). 309–313. 41 indexed citations
11.
Handler, Marc Z., et al.. (2013). Prevalence of Pilomatricoma in Turner Syndrome. JAMA Dermatology. 149(5). 559–559. 20 indexed citations
12.
Rush, Eric T., et al.. (2012). Evaluation and comparison of safety, convenience and cost of administering intravenous pamidronate infusions to children in the home and ambulatory care settings. Journal of Pediatric Endocrinology and Metabolism. 25(5-6). 493–7. 5 indexed citations
13.
Esposito, Paul W., et al.. (2011). The Incidence of Spondylolysis and Spondylolisthesis in Children With Osteogenesis Imperfecta. Journal of Pediatric Orthopaedics. 31(6). 655–660. 15 indexed citations
14.
Bishop, Nick, Cheryl R. Greenberg, Mairead McGinn, et al.. (2011). Life-threatening hypophosphatasia (HPP): Results of up to two years bone-targeted Enzyme Replacement Therapy (ERT) in infants and young children. Bone. 48. S82–S82. 1 indexed citations
15.
Lutz, Richard E., David Dimmock, Eric Schmitt, et al.. (2009). De Novo Mutations in POLG Presenting with Acute Liver Failure or Encephalopathy. Journal of Pediatric Gastroenterology and Nutrition. 49(1). 126–129. 8 indexed citations
16.
Ellis, Cynthia R., Richard E. Lutz, G. Bradley Schaefer, & Kathryn Woods. (2007). Physician collaboration involving students with Autism Spectrum Disorders. Psychology in the Schools. 44(7). 737–747. 13 indexed citations
17.
Lutz, Richard E.. (2007). Trinucleotide Repeat Disorders. Seminars in Pediatric Neurology. 14(1). 26–33. 16 indexed citations
18.
Schaefer, G. Bradley & Richard E. Lutz. (2006). Diagnostic yield in the clinical genetic evaluation of autism spectrum disorders. Genetics in Medicine. 8(9). 549–556. 70 indexed citations

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.

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