Mengfatt Ho

1.4k total citations
18 papers, 1.0k citations indexed

About

Mengfatt Ho is a scholar working on Molecular Biology, Physiology and Hematology. According to data from OpenAlex, Mengfatt Ho has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Hematology. Recurrent topics in Mengfatt Ho's work include Erythrocyte Function and Pathophysiology (5 papers), Muscle Physiology and Disorders (5 papers) and Blood groups and transfusion (5 papers). Mengfatt Ho is often cited by papers focused on Erythrocyte Function and Pathophysiology (5 papers), Muscle Physiology and Disorders (5 papers) and Blood groups and transfusion (5 papers). Mengfatt Ho collaborates with scholars based in United States, United Kingdom and Singapore. Mengfatt Ho's co-authors include Robert H. Brown, Anthony P. Monaco, Yukiko Hayashi, Kiichi Arahata, Chie Matsuda, Masahiro Nishijima, Kentaro Hanada, Walter M. Holleran, Masashi Aoki and Khemissa Bejaoui and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Blood.

In The Last Decade

Mengfatt Ho

18 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mengfatt Ho United States 14 612 358 267 187 163 18 1.0k
John P. Grady United Kingdom 22 1.1k 1.8× 140 0.4× 103 0.4× 208 1.1× 105 0.6× 51 1.4k
Konstantin Adamsky Israel 17 681 1.1× 101 0.3× 251 0.9× 171 0.9× 73 0.4× 25 1.3k
Sofia A. Oliveira Portugal 17 592 1.0× 135 0.4× 88 0.3× 230 1.2× 89 0.5× 29 1.2k
Hana S. Suidan Switzerland 15 516 0.8× 74 0.2× 435 1.6× 278 1.5× 64 0.4× 19 1.0k
Ji-Ung Jung United States 20 702 1.1× 228 0.6× 94 0.4× 143 0.8× 102 0.6× 29 1.3k
Thorsten Bangsow Germany 7 680 1.1× 97 0.3× 67 0.3× 142 0.8× 105 0.6× 13 1.1k
Yoshimitsu Yura Japan 15 400 0.7× 67 0.2× 323 1.2× 144 0.8× 57 0.3× 33 985
Li‐Chen Wu United States 8 1.2k 2.0× 408 1.1× 184 0.7× 44 0.2× 188 1.2× 15 1.6k
Paula Scotland United States 10 548 0.9× 156 0.4× 39 0.1× 218 1.2× 41 0.3× 15 817
Dominique Daegelen France 25 1.5k 2.4× 284 0.8× 37 0.1× 106 0.6× 363 2.2× 51 1.9k

Countries citing papers authored by Mengfatt Ho

Since Specialization
Citations

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

Fields of papers citing papers by Mengfatt Ho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mengfatt Ho

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

All Works

18 of 18 papers shown
1.
Zhu, Xiang, Eun-Sook Cho, Quan Sha, et al.. (2014). Giant Axon Formation in Mice Lacking Kell, XK, or Kell and XK. American Journal Of Pathology. 184(3). 800–807. 8 indexed citations
2.
Rivera, Alicia, et al.. (2012). Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis. Blood Cells Molecules and Diseases. 50(2). 80–85. 18 indexed citations
3.
Guo, Tiannan, Lingling Fan, Yi Zhu, et al.. (2012). Multidimensional Identification of Tissue Biomarkers of Gastric Cancer. Journal of Proteome Research. 11(6). 3405–3413. 12 indexed citations
4.
Hennessy, Thomas, Chee Sian Gan, Robin Philp, et al.. (2011). Characterization of the Human Gastric Fluid Proteome Reveals Distinct pH-Dependent Protein Profiles: Implications for Biomarker Studies. Journal of Proteome Research. 10(10). 4535–4546. 20 indexed citations
5.
Wenzel, Katrin, Claire L. Harris, Mengfatt Ho, et al.. (2005). Increased Susceptibility to Complement Attack due to Down-Regulation of Decay-Accelerating Factor/CD55 in Dysferlin-Deficient Muscular Dystrophy. The Journal of Immunology. 175(9). 6219–6225. 57 indexed citations
6.
Ho, Mengfatt. (2004). Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency. Human Molecular Genetics. 13(18). 1999–2010. 153 indexed citations
7.
Bejaoui, Khemissa, Yoshikazu Uchida, Satoshi Yasuda, et al.. (2002). Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis. Journal of Clinical Investigation. 110(9). 1301–1308. 67 indexed citations
8.
Bejaoui, Khemissa, Yoshikazu Uchida, Satoshi Yasuda, et al.. (2002). Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis. Journal of Clinical Investigation. 110(9). 1301–1308. 6 indexed citations
9.
Bejaoui, Khemissa, Yoshikazu Uchida, Satoshi Yasuda, et al.. (2002). Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis. Journal of Clinical Investigation. 110(9). 1301–1308. 68 indexed citations
10.
Danek, Adrian, Justin P. Rubio, Luca Rampoldi, et al.. (2001). McLeod neuroacanthocytosis: Genotype and phenotype. Annals of Neurology. 50(6). 755–764. 135 indexed citations
11.
Ho, Mengfatt, et al.. (2001). A novel, blood‐based diagnostic assay for limb girdle muscular dystrophy 2B and miyoshi myopathy. Annals of Neurology. 51(1). 129–133. 81 indexed citations
12.
Lee, Soohee, David Russo, Jeffrey J. Pu, Mengfatt Ho, & Colvin M. Redman. (2000). The mouse Kell blood group gene ( Kel ): cDNA sequence, genomic organization, expression, and enzymatic function. Immunogenetics. 52(1-2). 53–62. 13 indexed citations
13.
Matsuda, Chie, Masashi Aoki, Yukiko Hayashi, et al.. (1999). Dysferlin is a surface membrane–associated protein that is absent in Miyoshi myopathy. Neurology. 53(5). 1119–1119. 107 indexed citations
14.
Ho, Mengfatt, et al.. (1996). A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis. Annals of Neurology. 39(5). 672–675. 42 indexed citations
15.
16.
Blair, Helen J., Mengfatt Ho, Anthony P. Monaco, et al.. (1995). High-Resolution Comparative Mapping of the Proximal Region of the Mouse X Chromosome. Genomics. 28(2). 305–310. 15 indexed citations
17.
Ho, Mengfatt. (1994). Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. Cell. 77(6). 869–880. 187 indexed citations
18.
Ho, Mengfatt, Anthony P. Monaco, Lau A.J. Blonden, et al.. (1992). Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.. PubMed. 50(2). 317–30. 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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