A.M. Lamhonwah

548 total citations
8 papers, 473 citations indexed

About

A.M. Lamhonwah is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, A.M. Lamhonwah has authored 8 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 3 papers in Cell Biology. Recurrent topics in A.M. Lamhonwah's work include Metabolism and Genetic Disorders (4 papers), Biotin and Related Studies (2 papers) and Lysosomal Storage Disorders Research (2 papers). A.M. Lamhonwah is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Biotin and Related Studies (2 papers) and Lysosomal Storage Disorders Research (2 papers). A.M. Lamhonwah collaborates with scholars based in Canada, United States and United Kingdom. A.M. Lamhonwah's co-authors include R A Gravel, Don J. Mahuran, H.F. Willard, F Quan, J. A. Lowden, Katherine A. Siminovitch, Monica Peacocke, Krystyna Teichert-Kuliszewska, S M Weissman and Amro Shehabeldin and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Human Molecular Genetics.

In The Last Decade

A.M. Lamhonwah

8 papers receiving 465 citations

Peers

A.M. Lamhonwah

MB

PHYSI

CB

OC

Erin T. Strovel United States

Hideaki Hamazaki Japan

Noriyo Tokuda Japan

J Kreysing Germany

Seiichi Kawashima Japan

Jae-Sook Park United States

Sayuri Hara‐Kuge Japan

Fredrik Noborn Sweden

Vinayaga S. Gnanapragassam Germany

Izabella Niewczas United Kingdom

Erin T. Strovel United States

A.M. Lamhonwah

261 ×0.9

MB

73 ×0.5

PHYSI

272 ×1.9

CB

30 ×0.3

CB

36 ×0.6

OC

Citations per year, relative to A.M. Lamhonwah A.M. Lamhonwah (= 1×) peers Erin T. Strovel

Countries citing papers authored by A.M. Lamhonwah

Since Specialization

Citations

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

Fields of papers citing papers by A.M. Lamhonwah

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.M. Lamhonwah. 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 A.M. Lamhonwah. The network helps show where A.M. Lamhonwah may publish in the future.

Co-authorship network of co-authors of A.M. Lamhonwah

This figure shows the co-authorship network connecting the top 25 collaborators of A.M. Lamhonwah. A scholar is included among the top collaborators of A.M. Lamhonwah 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 A.M. Lamhonwah. A.M. Lamhonwah 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.

Lamhonwah, A.M., et al.. (2004). OCTN2 mutation (R254X) found in Saudi Arabian kindred: Recurrent mutation or ancient founder mutation?. Journal of Inherited Metabolic Disease. 27(4). 473–476. 6 indexed citations

2.

Siminovitch, Katherine A., et al.. (1999). Involvement of the SHP-1 Tyrosine Phosphatase in Regulating B Lymphocyte Antigen Receptor Signaling, Proliferation and Transformation. Current topics in microbiology and immunology. 246. 291–298. 17 indexed citations

3.

Shehabeldin, Amro, Monica Peacocke, A.M. Lamhonwah, et al.. (1995). Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus. Human Molecular Genetics. 4(7). 1119–1126. 92 indexed citations

4.

Gravel, R A, et al.. (1994). Mutations participating in interallelic complementation in propionic acidemia.. PubMed. 55(1). 51–8. 38 indexed citations

5.

Arpaia, Enrico, Anne Dumbrille-Ross, Kuldeep Neote, et al.. (1988). Identification of an altered splice site in Ashkenazi Tay-Sachs disease. Nature. 333(6168). 85–86. 123 indexed citations

6.

Lamhonwah, A.M. & R A Gravel. (1987). Propionicacidemia: absence of alpha-chain mRNA in fibroblasts from patients of the pccA complementation group.. PubMed. 41(6). 1124–31. 15 indexed citations

7.

Lamhonwah, A.M., et al.. (1986). Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes.. Proceedings of the National Academy of Sciences. 83(13). 4864–4868. 90 indexed citations

8.

O’Dowd, Brian F., F Quan, H.F. Willard, et al.. (1985). Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase.. Proceedings of the National Academy of Sciences. 82(4). 1184–1188. 92 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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