Lora Bean

1.2k total citations
8 papers, 795 citations indexed

About

Lora Bean is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Clinical Biochemistry. According to data from OpenAlex, Lora Bean has authored 8 papers receiving a total of 795 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 3 papers in Genetics and 2 papers in Clinical Biochemistry. Recurrent topics in Lora Bean's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Metabolism and Genetic Disorders (2 papers). Lora Bean is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Metabolism and Genetic Disorders (2 papers). Lora Bean collaborates with scholars based in United States. Lora Bean's co-authors include Emily G. Allen, Sallie B. Freeman, Stephanie L. Sherman, Wayne W. Grody, Adele Schneider, Anthony R. Gregg, Roger V. Lebo, Barry H. Thompson, Kristin G. Monaghan and Claudine P. Torfs and has published in prestigious journals such as Clinica Chimica Acta, Genetics in Medicine and Obstetrical & Gynecological Survey.

In The Last Decade

Lora Bean

7 papers receiving 736 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lora Bean United States	6	269	259	206	162	158	8	795
Nataliya Yuskiv Canada	10	217 0.8×	137 0.5×	181 0.9×	147 0.9×	87 0.6×	13	752
Anke Rißmann Germany	16	327 1.2×	134 0.5×	169 0.8×	191 1.2×	123 0.8×	57	901
Marjorie H. Royle United States	11	311 1.2×	243 0.9×	188 0.9×	190 1.2×	57 0.4×	21	831
Annukka Ritvanen Finland	19	682 2.5×	364 1.4×	146 0.7×	90 0.6×	96 0.6×	39	1.2k
Florian Faschingbauer Germany	20	537 2.0×	411 1.6×	114 0.6×	118 0.7×	93 0.6×	92	1.4k
Silvia Vannuccini Italy	22	344 1.3×	548 2.1×	120 0.6×	85 0.5×	43 0.3×	102	2.6k
Amy Bregar United States	16	184 0.7×	378 1.5×	121 0.6×	181 1.1×	89 0.6×	56	1.2k
G. Boog France	15	355 1.3×	116 0.4×	101 0.5×	84 0.5×	177 1.1×	93	766
Horacio Lejarraga Argentina	15	265 1.0×	104 0.4×	244 1.2×	54 0.3×	56 0.4×	71	751
Efthimios Deligeoroglou Greece	22	156 0.6×	503 1.9×	112 0.5×	114 0.7×	27 0.2×	73	1.3k

Countries citing papers authored by Lora Bean

Since Specialization

Citations

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

Fields of papers citing papers by Lora Bean

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lora Bean

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

All Works

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8 of 8 papers shown

1.

Fridovich‐Keil, Judith L., Lora Bean, Miao He, & Richard J. Schroer. (2016). Epimerase Deficiency Galactosemia. Europe PMC (PubMed Central). 15 indexed citations

2.

Liu, Ying, et al.. (2015). Genetic and functional studies reveal a novel noncoding variant in GALT associated with a false positive newborn screening result for galactosemia. Clinica Chimica Acta. 446. 171–174.

3.

Grody, Wayne W., Barry H. Thompson, Anthony R. Gregg, et al.. (2013). ACMG Position Statement on Prenatal/Preconception Expanded Carrier Screening. Obstetrical & Gynecological Survey. 68(12). 785–787. 5 indexed citations

4.

Askree, S. Hussain, Ephrem Chin, Lora Bean, et al.. (2013). Detection limit of intragenic deletions with targeted array comparative genomic hybridization. BMC Genetics. 14(1). 116–116. 14 indexed citations

5.

Hollis, NaTasha D., Emily G. Allen, Tiffany Oliver, et al.. (2013). Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project. American Journal of Medical Genetics Part A. 161(3). 438–444. 41 indexed citations

6.

Grody, Wayne W., Barry H. Thompson, Anthony R. Gregg, et al.. (2013). ACMG position statement on prenatal/preconception expanded carrier screening. Genetics in Medicine. 15(6). 482–483. 173 indexed citations

7.

Freeman, Sallie B., Lora Bean, Emily G. Allen, et al.. (2008). Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project. Genetics in Medicine. 10(3). 173–180. 204 indexed citations

8.

Sherman, Stephanie L., Emily G. Allen, Lora Bean, & Sallie B. Freeman. (2007). Epidemiology of Down syndrome. Mental Retardation and Developmental Disabilities Research Reviews. 13(3). 221–227. 343 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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