503 total citations 239 papers, 337 citations indexed
About
Mefford Hc is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry.
According to data from OpenAlex, Mefford Hc has authored 239 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 92 papers in Molecular Biology, 45 papers in Genetics and 35 papers in Clinical Biochemistry. Recurrent topics in Mefford Hc's work include Metabolism and Genetic Disorders (35 papers), Mitochondrial Function and Pathology (18 papers) and Genetic Neurodegenerative Diseases (13 papers). Mefford Hc is often cited by papers focused on Metabolism and Genetic Disorders (35 papers), Mitochondrial Function and Pathology (18 papers) and Genetic Neurodegenerative Diseases (13 papers). Mefford Hc collaborates with scholars based in . Mefford Hc's co-authors include Adam Mp, Pagon Ra, Bean Ljh, Ardinger Hh, Bird Td, A Amemiya, 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
Mefford Hc
193 papers
receiving
331 citations
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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This map shows the geographic impact of Mefford Hc'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 Mefford Hc with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mefford Hc more than expected).
This network shows the impact of papers produced by Mefford Hc. 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 Mefford Hc. The network helps show where Mefford Hc may publish in the future.
Co-authorship network of co-authors of Mefford Hc
This figure shows the co-authorship network connecting the top 25 collaborators of Mefford Hc.
A scholar is included among the top collaborators of Mefford Hc 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 Mefford Hc. Mefford Hc is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Progressive Myoclonus Epilepsy, Lafora Type -- GeneReviews®.
7.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). 15q24 Microdeletion Syndrome -- GeneReviews(®).1 indexed citations
8.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Hypertrophic Cardiomyopathy Overview -- GeneReviews®.1 indexed citations
9.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Mitochondrial DNA-Associated Leigh Syndrome and NARP -- GeneReviews®.3 indexed citations
10.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Alpha-Thalassemia -- GeneReviews(®).
11.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Gaucher Disease -- GeneReviews(®).4 indexed citations
12.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Autosomal Dominant Nocturnal Frontal Lobe Epilepsy -- GeneReviews(®).2 indexed citations
13.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Rothmund-Thomson Syndrome -- GeneReviews®.1 indexed citations
14.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). MED12-Related Disorders -- GeneReviews®.
15.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Polymicrogyria Overview -- GeneReviews®.1 indexed citations
16.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Spinal Muscular Atrophy, X-Linked Infantile -- GeneReviews(®).1 indexed citations
17.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Primary Ciliary Dyskinesia -- GeneReviews(®).
18.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Hemophagocytic Lymphohistiocytosis, Familial -- GeneReviews(®).1 indexed citations
19.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). TSEN54-Related Pontocerebellar Hypoplasia -- GeneReviews(®).1 indexed citations
20.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Diamond-Blackfan Anemia -- GeneReviews®.3 indexed citations
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive
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incomplete records, variations in author disambiguation, differences in journal indexing, and
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