Bean Ljh

575 total citations
285 papers, 386 citations indexed

About

Bean Ljh is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Bean Ljh has authored 285 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 110 papers in Molecular Biology, 55 papers in Genetics and 39 papers in Clinical Biochemistry. Recurrent topics in Bean Ljh's work include Metabolism and Genetic Disorders (39 papers), Mitochondrial Function and Pathology (19 papers) and Genetic Neurodegenerative Diseases (15 papers). Bean Ljh is often cited by papers focused on Metabolism and Genetic Disorders (39 papers), Mitochondrial Function and Pathology (19 papers) and Genetic Neurodegenerative Diseases (15 papers). Bean Ljh collaborates with scholars based in . Bean Ljh's co-authors include Adam Mp, Pagon Ra, Ardinger Hh, A Amemiya, Mefford Hc, Bird Td, Smith Rjh, Fong Ct, K Stephens and Adam C. Smith and has published in prestigious journals such as PLoS ONE, Memory & Cognition and Research Explorer (The University of Manchester).

In The Last Decade

Bean Ljh

231 papers receiving 379 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bean Ljh	6	180	113	56	46	37	285	386
Adam Mp	6	180 1.0×	113 1.0×	56 1.0×	46 1.0×	37 1.0×	286	388
Ardinger Hh United States	6	192 1.1×	124 1.1×	56 1.0×	46 1.0×	37 1.0×	287	402
A Amemiya Japan	6	173 1.0×	104 0.9×	53 0.9×	43 0.9×	37 1.0×	269	377
Bird Td United States	6	162 0.9×	90 0.8×	51 0.9×	41 0.9×	35 0.9×	244	342
Mefford Hc	6	163 0.9×	90 0.8×	51 0.9×	40 0.9×	35 0.9×	239	337
Fong Ct United States	6	141 0.8×	74 0.7×	38 0.7×	31 0.7×	23 0.6×	186	296
Florent Marguet France	13	187 1.0×	57 0.5×	30 0.5×	38 0.8×	60 1.6×	45	449
Morad Khayat Israel	16	422 2.3×	162 1.4×	115 2.1×	38 0.8×	46 1.2×	50	664
Hisato Suzuki Japan	12	277 1.5×	231 2.0×	23 0.4×	40 0.9×	49 1.3×	95	593
Geetha Anand United Kingdom	13	303 1.7×	105 0.9×	77 1.4×	34 0.7×	58 1.6×	34	565

Countries citing papers authored by Bean Ljh

Since Specialization

Citations

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

Fields of papers citing papers by Bean Ljh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bean Ljh

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

All Works

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20 of 20 papers shown

1.

Mp, Adam, et al.. (2020). Allan-Herndon-Dudley Syndrome -- GeneReviews®.

2.

Mp, Adam, Ardinger Hh, Pagon Ra, et al.. (2020). PAX6-Related Aniridia -- GeneReviews®. 1 indexed citations

3.

Mp, Adam, et al.. (2019). Arrhythmogenic Right Ventricular Cardiomyopathy -- GeneReviews®. 1 indexed citations

4.

Mp, Adam, Ardinger Hh, Pagon Ra, et al.. (2019). FARS2 Deficiency -- GeneReviews®. 1 indexed citations

5.

Mp, Adam, et al.. (2016). PLP1-Related Disorders -- GeneReviews(®). 6(4). 42–42. 1 indexed citations

6.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). ADAMTSL4-Related Eye Disorders -- GeneReviews®. 23(3).

7.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia -- GeneReviews(®). ACTA THERIOLOGICA. 57(4). 371–375. 1 indexed citations

8.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Chorea-Acanthocytosis -- GeneReviews(®). Memory & Cognition. 9(2). 164–8. 2 indexed citations

9.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Multiple Endocrine Neoplasia Type 2 -- GeneReviews(®). 1(1). 83–90. 1 indexed citations

10.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Neurofibromatosis 2 -- GeneReviews®. PLoS ONE. 13(12). e0208961–e0208961.

11.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Progressive Myoclonus Epilepsy, Lafora Type -- GeneReviews®.

12.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). 15q24 Microdeletion Syndrome -- GeneReviews(®). 1 indexed citations

13.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Hypertrophic Cardiomyopathy Overview -- GeneReviews®. 1 indexed citations

14.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Mitochondrial DNA-Associated Leigh Syndrome and NARP -- GeneReviews®. 3 indexed citations

15.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Alpha-Thalassemia -- GeneReviews(®).

16.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Gaucher Disease -- GeneReviews(®). 4 indexed citations

17.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Autosomal Dominant Nocturnal Frontal Lobe Epilepsy -- GeneReviews(®). 2 indexed citations

18.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Rothmund-Thomson Syndrome -- GeneReviews®. 1 indexed citations

19.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). MED12-Related Disorders -- GeneReviews®.

20.

Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Polymicrogyria Overview -- GeneReviews®. 1 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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