Frederick W. Luthardt

1.4k total citations
28 papers, 890 citations indexed

About

Frederick W. Luthardt is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Frederick W. Luthardt has authored 28 papers receiving a total of 890 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Frederick W. Luthardt's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Acute Myeloid Leukemia Research (4 papers). Frederick W. Luthardt is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Acute Myeloid Leukemia Research (4 papers). Frederick W. Luthardt collaborates with scholars based in United States, Norway and South Korea. Frederick W. Luthardt's co-authors include Arthur D. Riggs, Judith A. Singer, Roger P. Donahue, Cheryl L. Willman, Frederick R. Appelbaum, Catherine G. Palmer, Peng Yu, Kenneth J. Kopecky, Jeanne E. Anderson and Thomas H. Norwood and has published in prestigious journals such as Nucleic Acids Research, Blood and Human Molecular Genetics.

In The Last Decade

Frederick W. Luthardt

27 papers receiving 835 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frederick W. Luthardt United States 17 387 318 198 191 189 28 890
G.C. Beverstock Netherlands 14 318 0.8× 259 0.8× 51 0.3× 90 0.5× 198 1.0× 30 634
PatriciaA. Jacobs United Kingdom 14 510 1.3× 656 2.1× 110 0.6× 210 1.1× 148 0.8× 21 1.3k
Fiorella Shabtai Israel 17 229 0.6× 314 1.0× 84 0.4× 63 0.3× 116 0.6× 47 601
D E Rooney United Kingdom 10 245 0.6× 291 0.9× 72 0.4× 243 1.3× 68 0.4× 14 631
James Tepperberg United States 15 362 0.9× 532 1.7× 49 0.2× 284 1.5× 86 0.5× 28 889
F. J. Dill Canada 16 242 0.6× 579 1.8× 132 0.7× 486 2.5× 43 0.2× 24 897
F Salamanca Mexico 15 285 0.7× 287 0.9× 73 0.4× 89 0.5× 35 0.2× 60 709
Joy D.A. Delhanty United Kingdom 17 267 0.7× 290 0.9× 106 0.5× 423 2.2× 16 0.1× 30 796
Iris Bartels Germany 20 305 0.8× 643 2.0× 159 0.8× 738 3.9× 100 0.5× 69 1.3k
S Armendares Mexico 17 329 0.9× 435 1.4× 102 0.5× 149 0.8× 16 0.1× 65 863

Countries citing papers authored by Frederick W. Luthardt

Since Specialization
Citations

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

Fields of papers citing papers by Frederick W. Luthardt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frederick W. Luthardt. 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 Frederick W. Luthardt. The network helps show where Frederick W. Luthardt may publish in the future.

Co-authorship network of co-authors of Frederick W. Luthardt

This figure shows the co-authorship network connecting the top 25 collaborators of Frederick W. Luthardt. A scholar is included among the top collaborators of Frederick W. Luthardt 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 Frederick W. Luthardt. Frederick W. Luthardt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Byiringiro, Samuel, Sarah Stevens, Pamela Ouyang, et al.. (2022). Digital and virtual strategies to advance community stakeholder engagement in research during COVID-19 pandemic. Journal of Clinical and Translational Science. 6(1). e121–e121. 6 indexed citations
2.
Hong, Jeong-Yeon, et al.. (2005). Comparison of conscious sedation for oocyte retrieval between low-anxiety and high-anxiety patients. Journal of Clinical Anesthesia. 17(7). 549–553. 32 indexed citations
3.
Staats, Peter S., Frederick W. Luthardt, Jane Shipley, Catherine Joan Jackson, & Karl Fischer. (2001). Long-Term Intrathecal Ziconotide Therapy: A Case Study and Discussion. Neuromodulation Technology at the Neural Interface. 4(3). 121–126. 11 indexed citations
4.
Batanian, Jacqueline R., et al.. (2000). Trisomy 15 Is Frequently Observed as a Minor Clone in Patients with Anemia/ MDS/ NHL and as a Major Clone in Patients with AML. Cancer Genetics and Cytogenetics. 121(2). 186–189. 15 indexed citations
5.
6.
Bodner, Sara M., Clayton W. Naeve, Bart G. Jones, et al.. (1999). Cloning and chromosomal localization of the gene encoding human cyclin D-binding Myb-like protein (hDMP1). Gene. 229(1-2). 223–228. 30 indexed citations
7.
Resta, Robert G., Frederick W. Luthardt, & Raj P. Kapur. (1996). Follow-up of a familial translocation t(10;16) with an unusual segregation pattern. American Journal of Medical Genetics. 63(2). 363–365. 3 indexed citations
8.
Pettenati, Mark J., P. Nagesh Rao, Mary C. Phelan, et al.. (1995). Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases. American Journal of Medical Genetics. 55(2). 171–187. 82 indexed citations
9.
Nuñes, Mark E., Raj P. Kapur, Frederick W. Luthardt, et al.. (1995). A second autosomal split hand/split foot locus maps to chromosome 10q24-q25. Human Molecular Genetics. 4(11). 2165–2170. 60 indexed citations
10.
Cheng, Kwang‐Ting, et al.. (1995). Is the 15-in situ clone protocol necessary to detect amniotic fluid mosaicism?. American Journal of Obstetrics and Gynecology. 173(4). 1025–1030. 1 indexed citations
11.
Kapur, Raj P., et al.. (1993). Prenatal diagnosis of Tetraploidy: A case report. American Journal of Medical Genetics. 45(3). 378–382. 7 indexed citations
12.
Nyberg, David A., Robert G. Resta, B S Mahony, et al.. (1993). Fetal hyperechogenic bowel and Down's syndrome. Ultrasound in Obstetrics and Gynecology. 3(5). 330–333. 19 indexed citations
13.
Cheng, Kwang‐Ting, et al.. (1991). Transcervical chorionic villus sampling and midtrimester oligohydramnios. American Journal of Obstetrics and Gynecology. 165(4). 1063–1068. 4 indexed citations
14.
VanDevanter, Donald R., Diana George, Michael A. McNutt, Arthur Vogel, & Frederick W. Luthardt. (1991). Trisomy 8 in primary esthesioneuroblastoma. Cancer Genetics and Cytogenetics. 57(1). 133–136. 26 indexed citations
15.
Wyandt, Herman E., Nancy L. Fisher, Shivanand R. Patil, et al.. (1990). Trisomy 12 mosaicism in phenotypically normal fetuses following prenatal detection. Prenatal Diagnosis. 10(9). 569–574. 16 indexed citations
16.
Wilroy, R. Sid, Robert L. Summitt, Thomas N. Abdella, et al.. (1985). Genetic amniocentesis: A twelve years' experience. American Journal of Medical Genetics. 20(3). 443–452. 14 indexed citations
17.
Dabbous, Mustafa Kh., et al.. (1983). Cytogenetic analysis of collagenase-releasing rabbit VX-2 carcinoma-derived cells. Cancer Genetics and Cytogenetics. 8(2). 133–148. 5 indexed citations
18.
Singer, Judith A., et al.. (1979). Methylation of DNA in mouse early embryos, teratocarcinoma cells an adult tissues of mouse and rabbit. Nucleic Acids Research. 7(8). 2369–2385. 80 indexed citations
19.
Spence, M. Anne & Frederick W. Luthardt. (1975). Mitotic association patterns of nucleolar organizing chromosomes in the mouse. Cytogenetic and Genome Research. 15(4). 276–280. 5 indexed citations
20.
Luthardt, Frederick W. & Roger P. Donahue. (1975). DNA synthesis in developing two-cell mouse embryos. Developmental Biology. 44(1). 210–216. 38 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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