M Super

2.3k citations
48 papers · 1.7k · h-index 19

Impact in

  • Neurology top 5%
    • Neurofibromatosis and Schwannoma Cases
  • Genetics top 5%
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Cystic Fibrosis Research Advances 17
    • Tracheal and airway disorders 4
    • Neonatal Respiratory Health Research 4
    • Genomic variations and chromosomal abnormalities 3
    • Genomics and Rare Diseases 3

M Super

46 papers receiving 1.6k citations

Peers

M Super
Comparison fields: 5 of 92
  • Neurology 241
  • Genetics 444
  • Pulmonary and Respiratory Medicine 417
  • Physiology 305
  • Genetics 109
Replace Shirley Soukup with:
Shirley Soukup United States
R. Neil Schimke United States
Anne O’Meara Ireland
Marja W. Wessels Netherlands
Monica L. Calicchio United States
Boris G. Kousseff United States
Ingrid Laurendeau France
G A Lammie United Kingdom
Jonathan J. Rios United States
Kim M. Keppler‐Noreuil United States
M Super relative to Shirley Soukup United States Shirley Soukup's profile →
Citations per field
00.5×
Shirley Soukup · 1×
Citations per year

Countries citing papers authored by M Super

Since Specialization
Citations

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

Fields of papers citing papers by M Super

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M Super, 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 M Super Line = papers co-authored together M Super links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1994215
2
Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene.
1992209
3 1996194
4 1999159
5
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations.
2000102
6 1989101
7 198999
8 199794
9 199469
10 200154
11 199538
12 198836
13 198535
14 199330
15 199629
16 199925
17 199822
18 199220
19 199418
20 199017

About M Super

M Super is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 48 papers that have together received 1.7k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (17 papers), Prenatal Screening and Diagnostics (5 papers), Tumors and Oncological Cases (5 papers), Neurofibromatosis and Schwannoma Cases (4 papers), Tracheal and airway disorders (4 papers), Neonatal Respiratory Health Research (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Neurology (241 citations), Genetics (444 citations), Pulmonary and Respiratory Medicine (417 citations), Physiology (305 citations) and Genetics (109 citations). M Super has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Martin Schwarz, Geraldine Malone, G. H. Watson, D. Gareth Evans, M. Dawn Teare, Stephen F. Little, Dian Donnai, Hugh C. Smith, R G Patel and G. Hambleton. Their work appears in journals such as Archives of Disease in Childhood, Journal of Medical Genetics, Postgraduate Medical Journal, European Journal of Pediatrics and Clinical Genetics.

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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