N. Lannoy

489 total citations
20 papers, 303 citations indexed

About

N. Lannoy is a scholar working on Molecular Biology, Hematology and Physiology. According to data from OpenAlex, N. Lannoy has authored 20 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Hematology and 3 papers in Physiology. Recurrent topics in N. Lannoy's work include Hemophilia Treatment and Research (11 papers), Cancer-related gene regulation (9 papers) and Platelet Disorders and Treatments (7 papers). N. Lannoy is often cited by papers focused on Hemophilia Treatment and Research (11 papers), Cancer-related gene regulation (9 papers) and Platelet Disorders and Treatments (7 papers). N. Lannoy collaborates with scholars based in Belgium, United States and Netherlands. N. Lannoy's co-authors include Cédric Hermans, C. Verellen‐Dumoulin, Cédric Hermans, J. F. Gigot, Yves Pirson, Dorien J.M. Peters, Christine Verellen‐Dumoulin, M.H. Breuning, A Geubel and Catherine Lambert and has published in prestigious journals such as Hepatology, Journal of Medical Genetics and Human Mutation.

In The Last Decade

N. Lannoy

20 papers receiving 296 citations

Peers

Countries citing papers authored by N. Lannoy

Since Specialization

Citations

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

Fields of papers citing papers by N. Lannoy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Lannoy

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genetic mosaicism in haemophilia: A practical review to help evaluate the risk of transmitting the disease 2020 ·Haemophilia ·N. Lannoy, Cédric Hermans	12
2	Inhibitor epidemiology and genetic‐related risk factors in people with haemophilia from Côte d’Ivoire 2019 ·Haemophilia ·Catherine Lambert, N. Lannoy, (unknown), Ibrahima Sanogo, Stéphane Eeckhoudt, Cédric Hermans	3
3	Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia 2018 ·Haemophilia ·N. Lannoy, Cédric Hermans	6
4	Principles of genetic variations and molecular diseases: applications in hemophilia A 2016 ·Critical Reviews in Oncology/Hematology ·N. Lannoy, Cédric Hermans	20
5	Molecular analysis of simple and complex genetic variants in a cohort of patients with hemophilia A: Mechanisms and diagnostic implications 2015 ·Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)) ·N. Lannoy	1
6	Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence? 2015 ·Thrombosis Research ·N. Lannoy, Catherine Lambert, Miikka Vikkula, Cédric Hermans	5
7	Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A 2015 ·Haemophilia ·N. Lannoy, (unknown), Bernard Grisart, (unknown), (unknown), Miikka Vikkula, Cédric Hermans	4
8	Intron 22 homologous regions are implicated in exons 1–22 duplications of the F8 gene 2013 ·European Journal of Human Genetics ·N. Lannoy, Bernard Grisart, Stéphane Eeckhoudt, Christine Verellen‐Dumoulin, Catherine Lambert, Miikka Vikkula, Cédric Hermans	18
9	Functional Assessment ofTSC2Variants Identified in Individuals with Tuberous Sclerosis Complex 2013 ·Human Mutation ·Marianne Hoogeveen‐Westerveld, Rosemary Ekong, Sue Povey, Karin Mayer, N. Lannoy, Frances Elmslie, Martina Bebin, Kira A. Dies, Catherine Thompson, Steven Sparagana, Peter Maxwell Davies, Agnies M. van Eeghen, Elizabeth A. Thiele, Ans van den Ouweland, Dicky Halley, Mark Nellist	42
10	Functional Assessment ofTSC2 Variants Identified in Individuals with Tuberous Sclerosis Complex 2012 ·Human Mutation ·Marianne Hoogeveen‐Westerveld, Rosemary Ekong, (unknown), Karin Mayer, N. Lannoy, Frances Elmslie, (unknown), Kira A. Dies, Carl Thompson, Steven Sparagana, Peter Davies, Agnies M. van Eeghen, Dicky Halley, Mark Nellist	53
11	Prevalence and Spectrum of SDHx Mutations in Pheochromocytoma and Paraganglioma in Patients from Belgium: An Update 2012 ·Hormone and Metabolic Research ·Alexandre Persu, N. Lannoy, Dominique Maiter, Antonella Mendola, (unknown), Philippe Oriot, (unknown), P. Garin, Marc Hamoir, Miikka Vikkula	5
12	Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A 2011 ·Haemophilia ·N. Lannoy, (unknown), (unknown), Catherine Lambert, C. Vermylen, Cédric Hermans	10
13	Detection of factor IX gene mutations by high-resolution melting analysis 2010 ·Haemophilia ·(unknown), Cédric Hermans, (unknown), N. Lannoy	1
14	The ‘royal disease’– haemophilia A or B? A haematological mystery is finally solved 2010 ·Haemophilia ·N. Lannoy, Cédric Hermans	8
15	Identification of de novo deletion in the factor VIII gene by MLPA technique in two girls with isolated factor VIII deficiency 2009 ·Haemophilia ·N. Lannoy, (unknown), (unknown), Cédric Hermans	11
16	Homozygosity for facioscapulohumeral muscular dystrophy (FSHD) gene 2001 ·Neuromuscular Disorders ·(unknown), (unknown), N. Lannoy, (unknown), (unknown)	1
17	Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindreds 1997 ·Human Genetics ·(unknown), Alex Kartheuser, (unknown), (unknown), N. Lannoy, (unknown), Gerhard Mertens, Christine Verellen‐Dumoulin	37
18	The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screening. 1996 ·PubMed ·Alex Kartheuser, Sarah P. West, (unknown), Ann Curtis, (unknown), N. Lannoy, (unknown), (unknown), Peter Chapman, John Burn	8
19	Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2 1996 ·Hepatology ·Yves Pirson, N. Lannoy, Dorien J.M. Peters, A Geubel, J. F. Gigot, M.H. Breuning, C. Verellen‐Dumoulin	48
20	High CTG repeat number in nodular thyroid tissue from a myotonic dystrophy patient. 1994 ·Journal of Medical Genetics ·Chantal Daumerie, N. Lannoy, JP Squifflet, Gaston Verellen, C. Verellen‐Dumoulin	10

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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