Adam Mp

577 citations
286 papers · 388 · h-index 6

Impact in

    • Metabolism and Genetic Disorders
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • BRCA gene mutations in cancer

Papers in

    • Mitochondrial Function and Pathology 19
    • RNA regulation and disease 11
    • Genetics and Neurodevelopmental Disorders 14
    • Neurogenetic and Muscular Disorders Research 12
    • Genetic Syndromes and Imprinting 12

Adam Mp

232 papers receiving 381 citations

Peers

Adam Mp
Comparison fields: 5 of 72
  • Clinical Biochemistry 56
  • Genetics 113
  • Neurology 22
  • Molecular Biology 180
  • Genetics 27
Replace Bean Ljh with:
Bean Ljh
Ardinger Hh United States
A Amemiya Japan
Bird Td United States
Mefford Hc
Yaping Yang United States
Morad Khayat Israel
Fong Ct United States
Cristina Dias United Kingdom
Hisato Suzuki Japan
Adam Mp relative to Bean Ljh Bean Ljh's profile →
Citations per field
00.5×1.5×
Bean Ljh · 1×
Citations per year

Countries citing papers authored by Adam Mp

Since Specialization
Citations

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

Fields of papers citing papers by Adam Mp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 14 scholars most cited alongside Adam Mp, 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 Adam Mp Line = papers co-authored together Adam Mp links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 286 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Neurodegeneration with Brain Iron Accumulation Disorders Overview -- GeneReviews(®)
20167
2
Neurofibromatosis 1 -- GeneReviews(®)
20166
3
Classic Galactosemia and Clinical Variant Galactosemia -- GeneReviews(®)
20165
4
Fibrous Dysplasia/McCune-Albright Syndrome -- GeneReviews(®)
20165
5
Juvenile Polyposis Syndrome -- GeneReviews(®)
20165
6
Mitochondrial Disorders Overview -- GeneReviews(®)
20165
7
AP-4-Associated Hereditary Spastic Paraplegia -- GeneReviews®
20195
8
Barth Syndrome -- GeneReviews®
20165
9
Prader-Willi Syndrome -- GeneReviews®
20164
10
Gaucher Disease -- GeneReviews(®)
20164
11
Disorders of Intracellular Cobalamin Metabolism -- GeneReviews®
20164
12
Hereditary Paraganglioma-Pheochromocytoma Syndromes -- GeneReviews®
20164
13
PTEN Hamartoma Tumor Syndrome -- GeneReviews®
20164
14
Spinocerebellar Ataxia Type 8 -- GeneReviews(®)
20164
15
Urea Cycle Disorders Overview -- GeneReviews(®)
20164
16
Niemann-Pick Disease Type C -- GeneReviews®
20164
17
Mitochondrial DNA Deletion Syndromes -- GeneReviews®
20164
18
Wilson Disease -- GeneReviews(®)
20163
19
Diamond-Blackfan Anemia -- GeneReviews®
20163
20
Mitochondrial DNA-Associated Leigh Syndrome and NARP -- GeneReviews®
20163

About Adam Mp

Adam Mp is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience and Rheumatology, having authored 286 papers that have together received 388 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (39 papers), Mitochondrial Function and Pathology (19 papers), Genetic Neurodegenerative Diseases (15 papers), Genetics and Neurodevelopmental Disorders (14 papers), Neurogenetic and Muscular Disorders Research (12 papers), Genetic Syndromes and Imprinting (12 papers), RNA regulation and disease (11 papers) and Lysosomal Storage Disorders Research (10 papers). The work is most often cited by research in Clinical Biochemistry (56 citations), Genetics (113 citations), Neurology (22 citations), Molecular Biology (180 citations) and Genetics (27 citations). Frequent co-authors include Ardinger Hh, Pagon Ra, Bean Ljh, A Amemiya, Mefford Hc, Bird Td, Smith Rjh, Fong Ct, K Stephens and Adam C. Smith. Their work appears in journals such as Memory & Cognition, PLoS ONE, Research Padua Archive (University of Padua), Research Explorer (The University of Manchester) and ACTA THERIOLOGICA.

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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