Mefford Hc

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 · hero ref

Name h Career Trend Papers Cites
Mefford Hc 6 163 90 51 40 35 239 337
Bird Td United States 6 162 1.0× 90 1.0× 51 1.0× 41 1.0× 35 1.0× 244 342
Bean Ljh 6 180 1.1× 113 1.3× 56 1.1× 46 1.1× 37 1.1× 285 386
A Amemiya Japan 6 173 1.1× 104 1.2× 53 1.0× 43 1.1× 37 1.1× 269 377
Adam Mp 6 180 1.1× 113 1.3× 56 1.1× 46 1.1× 37 1.1× 286 388
Ardinger Hh United States 6 192 1.2× 124 1.4× 56 1.1× 46 1.1× 37 1.1× 287 402
Fong Ct United States 6 141 0.9× 74 0.8× 38 0.7× 31 0.8× 23 0.7× 186 296
Florent Marguet France 13 187 1.1× 57 0.6× 30 0.6× 38 0.9× 60 1.7× 45 449
Bret L. Bostwick United States 9 225 1.4× 215 2.4× 35 0.7× 43 1.1× 35 1.0× 17 414
Geetha Anand United Kingdom 13 303 1.9× 105 1.2× 77 1.5× 34 0.8× 58 1.7× 34 565
Luigina Spaccini Italy 13 208 1.3× 159 1.8× 39 0.8× 43 1.1× 28 0.8× 47 455

Countries citing papers authored by Mefford Hc

Since Specialization
Citations

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).

Fields of papers citing papers by Mefford Hc

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

All Works

20 of 20 papers shown
1.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). ADAMTSL4-Related Eye Disorders -- GeneReviews®. 23(3).
2.
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
3.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Chorea-Acanthocytosis -- GeneReviews(®). Memory & Cognition. 9(2). 164–8. 2 indexed citations
4.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Multiple Endocrine Neoplasia Type 2 -- GeneReviews(®). 1(1). 83–90. 1 indexed citations
5.
Ra, Pagon, Adam Mp, Ardinger Hh, et al.. (2016). Neurofibromatosis 2 -- GeneReviews®. PLoS ONE. 13(12). e0208961–e0208961.
6.
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 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026