Lam Son Nguyen

2.4k citations

21 papers · 1.2k indexed · h-index 17

Co-authors: Jozef Gécz Miles Wilkinson Laurence Colleaux Julien Fregeac Eric Haan Karine Siquier-Pernet Martine Raynaud James Rutledge
Topics: Genetics and Neurodevelopmental Disorders (8 papers)RNA Research and Splicing (8 papers)RNA modifications and cancer (6 papers)
Cited by: Genetics Molecular Biology Cancer Research
Journals: The FASEB Journal Neuroscience & Biobehavioral Reviews The American Journal of Human Genetics
Partner nations: Australia France United States

In The Last Decade

Lam Son Nguyen

21 papers receiving 1.2k citations

Peers

Countries citing papers authored by Lam Son Nguyen

Since Specialization

Citations

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

Fields of papers citing papers by Lam Son Nguyen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lam Son Nguyen. 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 Lam Son Nguyen. The network helps show where Lam Son Nguyen may publish in the future.

Co-authorship network of co-authors of Lam Son Nguyen

This figure shows the co-authorship network connecting the top 25 collaborators of Lam Son Nguyen. A scholar is included among the top collaborators of Lam Son Nguyen 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 Lam Son Nguyen. Lam Son Nguyen 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	Loss of the neurodevelopmental disease-associated gene miR-146a impairs neural progenitor differentiation and causes learning and memory deficits 2020 ·Molecular Autism ·Julien Fregeac,Stéphanie Moriceau,(unknown),Lam Son Nguyen,Franck Oury,Laurence Colleaux	27
2	Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders 2018 ·Molecular Autism ·Lam Son Nguyen,Julien Fregeac,Christine Bôle‐Feysot,Nicolas Cagnard,Anand M. Iyer,Jasper J. Anink,Eleonora Aronica,Olivier Alibeu,Patrick Nitschké,Laurence Colleaux	73
3	Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance 2018 ·European Journal of Human Genetics ·Matthieu Egloff,Lam Son Nguyen,Karine Siquier-Pernet,Valérie Cormier‐Daire,Geneviève Baujat,Tania Attié‐Bitach,Christine Bôle‐Feysot,Patrick Nitschké,Michel Vekemans,Laurence Colleaux,Valérie Malan	9
4	Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability 2018 ·American Journal of Medical Genetics Part A ·Nguyễn Huy Hoàng,(unknown),Giulia Barcia,Valérie Malan,(unknown),(unknown),(unknown),P. Landrieu,Laurence Colleaux,Nông Văn Hải,Lam Son Nguyen	2
5	The emerging roles of MicroRNAs in autism spectrum disorders 2016 ·Neuroscience & Biobehavioral Reviews ·Julien Fregeac,Laurence Colleaux,Lam Son Nguyen	42
6	Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology 2016 ·Molecular Autism ·Lam Son Nguyen,Marylin Lepleux,M. Makhlouf,Christelle Martin,Julien Fregeac,Karine Siquier-Pernet,Anne Philippe,François Féron,Bruno Gepner,Claire Rougeulle,Yann Humeau,Laurence Colleaux	131
7	A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy 2015 ·European Journal of Human Genetics ·Lam Son Nguyen,Taiane Schneider,Marlène Rio,Sébastien Moutton,Karine Siquier-Pernet,(unknown),Nathalie Boddaert,Isabelle Desguerre,(unknown),José Luís Rosa,Valérie Cormier‐Daire,Laurence Colleaux	39
8	A conserved MADS-box phosphorylation motif regulates differentiation and mitochondrial function in skeletal, cardiac, and smooth muscle cells 2015 ·Cell Death and Disease ·(unknown),Lam Son Nguyen,(unknown),Simone C. da Silva Rosa,(unknown),Donald Chapman,‬Min Du,(unknown),Jörg Grigull,Andrew J. Halayko,Michel Aliani,Matthew K. Topham,Richard M. Epand,Grant M. Hatch,Troy J. Pereira,Stephanie M. Kereliuk,John C. McDermott,Christof Rampitsch,Vernon W. Dolinsky,Joseph W. Gordon	41
9	Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy 2015 ·Molecular Psychiatry ·G. McMichael,Matthew N. Bainbridge,Eric Haan,Mark Corbett,Alison Gardner,(unknown),Bregje W.M. van Bon,Clare L. van Eyk,J. L. BROADBENT,Chandra A. Reynolds,Michael O’Callaghan,Lam Son Nguyen,David L. Adelson,Remo Russo,Shalini N. Jhangiani,HarshaVardhan Doddapaneni,Donna M. Muzny,Richard A. Gibbs,Jozef Gécz,Alastair H. MacLennan	147
10	HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain 2015 ·Human Molecular Genetics ·Lachlan A. Jolly,Lam Son Nguyen,Deepti Domingo,(unknown),Simon C. Barry,Miroslava Hančárová,Pavlína Plevová,Markéta Vlčková,Markéta Havlovičová,Vera M. Kalscheuer,Claudio Graziano,Tommaso Pippucci,Elena Bonora,Zdeněk Sedláček,Jozef Gécz	42
11	Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth 2014 ·The American Journal of Human Genetics ·Claire C. Homan,Raman Kumar,Lam Son Nguyen,Eric Haan,F. Lucy Raymond,Fatima Abidi,Martine Raynaud,Charles E. Schwartz,Stephen A. Wood,Jozef Gécz,Lachlan A. Jolly	100
12	Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders 2013 ·Human Molecular Genetics ·Lam Son Nguyen,Hyung‐Goo Kim,Jill A. Rosenfeld,Yiping Shen,James F. Gusella,Yves Lacassie,Lawrence C. Layman,Lisa G. Shaffer,Jozef Gécz	116
13	Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability 2013 ·Human Molecular Genetics ·Mireille Melko,Lam Son Nguyen,Marie Shaw,Lachlan A. Jolly,Barbara Bardoni,Jozef Gécz	10
14	Nonsense-mediated mRNA decay: Inter-individual variability and human disease 2013 ·Neuroscience & Biobehavioral Reviews ·Lam Son Nguyen,Miles Wilkinson,Jozef Gécz	98
15	Rare copy number variation in cerebral palsy 2013 ·European Journal of Human Genetics ·G. McMichael,Santhosh Girirajan,Andrés Moreno-De-Luca,Jozef Gécz,(unknown),Lam Son Nguyen,Jillian Nicholl,Catherine Gibson,Eric Haan,Evan E. Eichler,Christa Lese Martin,Alastair H. MacLennan	49
16	Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay 2012 ·European Journal of Medical Genetics ·Sally Ann Lynch,Lam Son Nguyen,(unknown),Mary Waldron,Denise McDonald,Jozef Gécz	30
17	NMD‐deficient Upf3b‐null mice display behavioral and neuropathological defects 2012 ·The FASEB Journal ·Lulu Huang,Eleen Y. Shum,Rachid Karam,Lam Son Nguyen,Jozef Gécz,Miles Wilkinson	1
18	A UPF3-mediated regulatory switch that maintains RNA surveillance 2009 ·Nature Structural & Molecular Biology ·Wai-Kin Chan,Angela D. Bhalla,Hervé Le Hir,Lam Son Nguyen,Lulu Huang,Jozef Gécz,Miles Wilkinson	94
19	Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism 2009 ·Molecular Psychiatry ·Frédéric Laumonnier,Cheryl Shoubridge,Catherine Antar,Lam Son Nguyen,Hilde Van Esch,Tjitske Kleefstra,Sylvain Briault,J. P. Fryns,B Hamel,Jamel Chelly,Hans‐Hilger Ropers,Nathalie Ronce,(unknown),Claude Moraine,Jozef Gécz,Martine Raynaud	89
20	Substance P increases microvascular permeability via nitric oxide-mediated convective pathways 1995 ·American Journal of Physiology-Regulatory, Integrative and Comparative Physiology ·Lam Son Nguyen,Amparo C. Villablanca,James Rutledge	43

About Lam Son Nguyen

Lam Son Nguyen is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 21 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), RNA Research and Splicing (8 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Genetics (352 citations), Molecular Biology (785 citations) and Cancer Research (167 citations). Lam Son Nguyen has collaborated with scholars based in Australia, France and United States. Frequent co-authors include Jozef Gécz, Miles Wilkinson, Laurence Colleaux, Julien Fregeac, Eric Haan, Karine Siquier-Pernet, Martine Raynaud, James Rutledge, Lulu Huang and Lachlan A. Jolly. Their work appears in journals such as The FASEB Journal, Neuroscience & Biobehavioral Reviews and The American Journal of Human 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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