Mefford Hc

503 citations

239 papers · 337 indexed · h-index 6

Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders 35
Genetics
- Genetic Syndromes and Imprinting 11
- Neurogenetic and Muscular Disorders Research 10
Molecular Biology
- Mitochondrial Function and Pathology 18
- RNA regulation and disease 10
- Biochemical and Molecular Research 9
Genetics
- Genetic Syndromes and Imprinting 11
- Neurogenetic and Muscular Disorders Research 10
Cellular and Molecular Neuroscience
- Genetic Neurodegenerative Diseases 13
Biochemistry
- Amino Acid Enzymes and Metabolism 9

Co-authors: Adam Mp Pagon Ra Bean Ljh Ardinger Hh Bird Td A Amemiya Smith Rjh Fong Ct
Cited by: Clinical Biochemistry Genetics Molecular Biology
Journals: PLoS ONE (1 paper)Memory & Cognition (1 paper)Research Explorer (The University of Manchester) (1 paper)

In The Last Decade

Mefford Hc

193 papers receiving 331 citations

Peers

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

The 14 scholars most cited alongside Mefford Hc, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mefford Hc Line = papers co-authored together Mefford Hc links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	ADAMTSL4-Related Eye Disorders -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	0
2	21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia -- GeneReviews(®) ACTA THERIOLOGICA ·Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	1
3	Chorea-Acanthocytosis -- GeneReviews(®) Memory & Cognition ·Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	2
4	Multiple Endocrine Neoplasia Type 2 -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	1
5	Neurofibromatosis 2 -- GeneReviews® PLoS ONE ·Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	0
6	Progressive Myoclonus Epilepsy, Lafora Type -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	0
7	15q24 Microdeletion Syndrome -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Nikki Ledbetter,Mefford Hc,Adam C. Smith,K Stephens	2016	1
8	Hypertrophic Cardiomyopathy Overview -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	1
9	Mitochondrial DNA-Associated Leigh Syndrome and NARP -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Nikki Ledbetter,Mefford Hc,Smith Rjh,Karen Stephens	2016	3
10	Alpha-Thalassemia -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	0
11	Gaucher Disease -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	4
12	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Nikki Ledbetter,Mefford Hc,Smith Rjh,K Stephens	2016	2
13	Rothmund-Thomson Syndrome -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	1
14	MED12-Related Disorders -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Adam C. Smith,K Stephens	2016	0
15	Polymicrogyria Overview -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Adam C. Smith,K Stephens	2016	1
16	Spinal Muscular Atrophy, X-Linked Infantile -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	1
17	Primary Ciliary Dyskinesia -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K. Stephens	2016	0
18	Hemophagocytic Lymphohistiocytosis, Familial -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Nikki Ledbetter,Mefford Hc,Smith Rjh,K Stephens	2016	1
19	TSEN54-Related Pontocerebellar Hypoplasia -- GeneReviews(®) Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	1
20	Diamond-Blackfan Anemia -- GeneReviews® Pagon Ra,Adam Mp,Ardinger Hh,Wallace Se,A Amemiya,Bean Ljh,Bird Td,Fong Ct,Mefford Hc,Smith Rjh,K Stephens	2016	3

About Mefford Hc

Mefford Hc is a scholar working on Clinical Biochemistry, Biochemistry and Genetics, having authored 239 papers that have together received 337 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (35 papers), Mitochondrial Function and Pathology (18 papers), Genetic Neurodegenerative Diseases (13 papers), Genetic Syndromes and Imprinting (11 papers), RNA regulation and disease (10 papers), Neurogenetic and Muscular Disorders Research (10 papers), Biochemical and Molecular Research (9 papers) and Amino Acid Enzymes and Metabolism (9 papers). The work is most often cited by research in Clinical Biochemistry (51 citations), Genetics (90 citations) and Molecular Biology (163 citations). Frequent 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. Their work appears in journals such as PLoS ONE, Memory & Cognition and Research Explorer (The University of Manchester).

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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