M E Oude Luttikhuis

479 citations
9 papers · 355 indexed · h-index 8
Topics
Genetic Syndromes and Imprinting (4 papers)Neuroblastoma Research and Treatments (3 papers)Genomics and Rare Diseases (2 papers)

In The Last Decade

M E Oude Luttikhuis

9 papers receiving 350 citations

Peers

M E Oude Luttikhuis
Comparison fields: 5 of 39
  • Genetics 256
  • Molecular Biology 221
  • Neurology 61
  • Cancer Research 42
  • Oncology 38
Replace Jocelyne Attia‐Sobol with:
Jocelyne Attia‐Sobol France
Hirofumi Ohashi Japan
Kiyoshi Kikkawa Japan
Geneviève Pierquin Belgium
Angela L. Duker United States
Randi Koll Germany
A Baxová Czechia
Heide Seidel Germany
Mary Haddadin United States
Emma Hobson United Kingdom
M E Oude Luttikhuis relative to Jocelyne Attia‐Sobol France Jocelyne Attia‐Sobol's profile →
Citations per field
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Jocelyne Attia‐Sobol · 1×
Citations per year

Countries citing papers authored by M E Oude Luttikhuis

Since Specialization
Citations

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

Fields of papers citing papers by M E Oude Luttikhuis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M E Oude Luttikhuis

This figure shows the co-authorship network connecting the top 25 collaborators of M E Oude Luttikhuis. A scholar is included among the top collaborators of M E Oude Luttikhuis 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 M E Oude Luttikhuis. M E Oude Luttikhuis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

9 of 9 papers shown
#WorkIndexed citations
1 8
2 51
3 7
4 34
5 9
6 5
7
Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.
105
8 30
9 106

About M E Oude Luttikhuis

M E Oude Luttikhuis is a scholar working on Developmental Biology, Neurology and Genetics, having authored 9 papers that have together received 355 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Neuroblastoma Research and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (256 citations), Developmental Biology (15 citations) and Neurology (61 citations). M E Oude Luttikhuis has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Richard C. Trembath, Louise C. Wilson, William D. Fraser, Peter T. Clayton, Drew Duckett, Jane Wolstenholme, Jonathan Flint, Carmel McConville, James V. Leonard and Shaheen Chughtai. Their work appears in journals such as British Journal of Cancer, Genomics and Journal of Medical 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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