Lee Fallon

772 total citations
10 papers, 214 citations indexed

About

Lee Fallon is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Lee Fallon has authored 10 papers receiving a total of 214 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Lee Fallon's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and BRCA gene mutations in cancer (2 papers). Lee Fallon is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and BRCA gene mutations in cancer (2 papers). Lee Fallon collaborates with scholars based in United States. Lee Fallon's co-authors include Joseph D. Schulman, Susan H. Black, Gene Levinson, G. Harton, Patricia N. Howard‐Peebles, David Bick, Wayne S. Stanley, H. Stern, Frances T. Palmer and Keyvan Keyvanfar and has published in prestigious journals such as Neurology, Human Reproduction and Molecular Human Reproduction.

In The Last Decade

Lee Fallon

10 papers receiving 210 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lee Fallon United States	7	127	93	57	38	35	10	214
Frances T. Palmer United States	8	112 0.9×	96 1.0×	56 1.0×	16 0.4×	44 1.3×	10	341
Miriam S. DiMaio United States	9	229 1.8×	211 2.3×	101 1.8×	34 0.9×	31 0.9×	14	355
B. Pettersen United States	8	254 2.0×	207 2.2×	77 1.4×	51 1.3×	19 0.5×	12	406
Elena Lopez‐Rangel Canada	11	50 0.4×	142 1.5×	97 1.7×	33 0.9×	21 0.6×	19	297
J. Dreesen Netherlands	9	213 1.7×	143 1.5×	179 3.1×	8 0.2×	26 0.7×	14	361
Ting Bai China	10	112 0.9×	101 1.1×	99 1.7×	35 0.9×	43 1.2×	29	301
Jenny Morton United Kingdom	6	27 0.2×	122 1.3×	90 1.6×	68 1.8×	8 0.2×	8	236
Yanhui Liu China	8	50 0.4×	61 0.7×	69 1.2×	11 0.3×	20 0.6×	22	194
Angelique J. A. Kooper Netherlands	13	289 2.3×	178 1.9×	35 0.6×	7 0.2×	58 1.7×	20	359
Jane Trussler United Kingdom	5	151 1.2×	110 1.2×	169 3.0×	5 0.1×	27 0.8×	5	308

Countries citing papers authored by Lee Fallon

Since Specialization

Citations

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

Fields of papers citing papers by Lee Fallon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lee Fallon. 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 Lee Fallon. The network helps show where Lee Fallon may publish in the future.

Co-authorship network of co-authors of Lee Fallon

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

All Works

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10 of 10 papers shown

1.

Fallon, Lee, et al.. (2021). 56 Paternal contributions to early embryonic stress affect development in the bovine. Reproduction Fertility and Development. 34(2). 263–264. 1 indexed citations

2.

Stern, H., et al.. (2002). Non‐disclosing preimplantation genetic diagnosis for Huntington disease. Prenatal Diagnosis. 22(6). 503–507. 34 indexed citations

3.

Fallon, Lee, et al.. (2002). Reproductive Options for Individuals at Risk for Transmission of a Genetic Disorder. Journal of Obstetric, Gynecologic & Neonatal Nursing. 31(2). 193–199. 11 indexed citations

4.

Li, Marilyn M., et al.. (2000). Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis. Prenatal Diagnosis. 20(2). 138–143. 6 indexed citations

5.

Howard‐Peebles, Patricia N., et al.. (2000). Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis. Prenatal Diagnosis. 20(2). 138–143. 22 indexed citations

6.

Fallon, Lee, G. Harton, Emma Rodrı́guez, et al.. (1999). Preimplantation genetic diagnosis for spinal muscular atrophy type I. Neurology. 53(5). 1087–1087. 33 indexed citations

7.

Black, Susan H., Lee Fallon, Anne Maddalena, et al.. (1996). Molecular fragile X screening in normal populations. American Journal of Medical Genetics. 64(1). 181–183. 40 indexed citations

8.

Black, Susan H., Lee Fallon, Anne Maddalena, et al.. (1996). Molecular fragile X screening in normal populations. American Journal of Medical Genetics. 64(1). 181–183. 4 indexed citations

9.

Huffman, J.L., Jianfeng Wu, Frances T. Palmer, et al.. (1995). Diagnosing and preventing inherited disease: Nucleated erythrocytes in maternal blood: quantity and quality of fetal cells in enriched populations. Human Reproduction. 10(9). 2510–2515. 42 indexed citations

10.

Palmer, Frances T., G. Harton, Keyvan Keyvanfar, et al.. (1995). Nucleated erythrocytes in maternal blood: quantity and quality of fetal cells in enriched populations. Molecular Human Reproduction. 1(7). 362–367. 21 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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