M E Oude Luttikhuis

479 total citations
9 papers, 355 citations indexed

About

M E Oude Luttikhuis is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, M E Oude Luttikhuis has authored 9 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Neurology. Recurrent topics in M E Oude Luttikhuis's work include Genetic Syndromes and Imprinting (4 papers), Neuroblastoma Research and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). M E Oude Luttikhuis is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Neuroblastoma Research and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). M E Oude Luttikhuis collaborates with scholars based in United Kingdom, United States and Netherlands. M E Oude Luttikhuis's co-authors include Richard C. Trembath, Louise C. Wilson, William D. Fraser, Peter T. Clayton, Drew Duckett, Jonathan Flint, Jane Wolstenholme, Carmel McConville, James V. Leonard and Shaheen Chughtai and has published in prestigious journals such as British Journal of Cancer, Genomics and Journal of Medical Genetics.

In The Last Decade

M E Oude Luttikhuis

9 papers receiving 350 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
M E Oude Luttikhuis United Kingdom	8	256	221	61	42	38	9	355
Angela L. Duker United States	10	267 1.0×	284 1.3×	28 0.5×	72 1.7×	17 0.4×	25	471
Mary Haddadin United States	6	103 0.4×	210 1.0×	23 0.4×	38 0.9×	60 1.6×	7	343
Randi Koll Germany	9	152 0.6×	206 0.9×	8 0.1×	31 0.7×	46 1.2×	13	346
Jocelyne Attia‐Sobol France	8	64 0.3×	99 0.4×	45 0.7×	35 0.8×	35 0.9×	10	240
Geneviève Pierquin Belgium	10	173 0.7×	188 0.9×	15 0.2×	13 0.3×	18 0.5×	24	318
Hirofumi Ohashi Japan	11	125 0.5×	198 0.9×	15 0.2×	12 0.3×	16 0.4×	12	321
Venkateswara R. Potluri United States	7	195 0.8×	141 0.6×	34 0.6×	24 0.6×	58 1.5×	10	321
Kiyoshi Kikkawa Japan	12	211 0.8×	182 0.8×	15 0.2×	23 0.5×	13 0.3×	27	378
Heide Seidel Germany	14	192 0.8×	182 0.8×	12 0.2×	9 0.2×	18 0.5×	24	337
A Baxová Czechia	10	246 1.0×	243 1.1×	5 0.1×	24 0.6×	29 0.8×	40	416

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

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9 of 9 papers shown

McConville, Carmel, Sara Dyer, M E Oude Luttikhuis, et al.. (2001). Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17). Cancer Genetics and Cytogenetics. 130(2). 133–140. 8 indexed citations

Luttikhuis, M E Oude, et al.. (2001). Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis. British Journal of Cancer. 85(4). 531–537. 51 indexed citations

Luttikhuis, M E Oude, et al.. (2000). Detection of MYCN Amplification in Neuroblastoma using Competitive PCR Quantitation. Laboratory Investigation. 80(2). 271–273. 7 indexed citations

Bijlsma, Emilia K., Cora M. Aalfs, M E Oude Luttikhuis, et al.. (1999). Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype. Journal of Medical Genetics. 36(8). 604–609. 34 indexed citations

Wilson, Louise C., M E Oude Luttikhuis, M Baraitser, H. M. Kingston, & Richard C. Trembath. (1997). Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosis.. Journal of Medical Genetics. 34(2). 133–136. 9 indexed citations

Luttikhuis, M E Oude, David Williams, & Richard C. Trembath. (1996). Isolated autosomal dominant type E brachydactyly: exclusion of linkage to candidate regions 2q37 and 20q13.. Journal of Medical Genetics. 33(10). 873–876. 5 indexed citations

Luttikhuis, M E Oude, et al.. (1995). Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.. PubMed. 56(2). 400–7. 105 indexed citations

Wilson, Louise C., M E Oude Luttikhuis, Peter T. Clayton, William D. Fraser, & Richard C. Trembath. (1994). Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.. Journal of Medical Genetics. 31(11). 835–839. 106 indexed citations

Luttikhuis, M E Oude, Louise C. Wilson, James V. Leonard, & Richard C. Trembath. (1994). Characterization of a de Novo 43-bp Deletion of the Gsα Gene (GNAS1) in Albright Hereditary Osteodystrophy. Genomics. 21(2). 455–457. 30 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.

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