Lam Son Nguyen

2.4k citations

21 papers · 1.2k indexed · h-index 17

Genetics top 5%
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 5
Molecular Biology top 10%
- RNA Research and Splicing 8
- RNA modifications and cancer 6
- RNA and protein synthesis mechanisms 3
- Receptor Mechanisms and Signaling 2
Cancer Research top 10%
- MicroRNA in disease regulation 5
Genetics top 10%
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 5
Cognitive Neuroscience top 10%

Co-authors: Jozef Gécz Miles Wilkinson Laurence Colleaux Julien Fregeac Eric Haan Karine Siquier-Pernet Martine Raynaud James Rutledge
Cited by: Genetics Molecular Biology Cancer Research
Journals: The FASEB Journal (1 paper)Neuroscience & Biobehavioral Reviews (2 papers)The American Journal of Human Genetics (1 paper)
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

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

All Works

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20 of 20 papers shown

#	Work
1	Loss of the neurodevelopmental disease-associated gene miR-146a impairs neural progenitor differentiation and causes learning and memory deficits Molecular Autism ·Julien Fregeac,Stéphanie Moriceau,Antoine Poli,Lam Son Nguyen,Franck Oury,Laurence Colleaux	2020	27
2	Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders 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	2018	73
3	Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance 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	2018	9
4	Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability American Journal of Medical Genetics Part A ·Nguyễn Huy Hoàng,Van Anh Pham,Giulia Barcia,Valérie Malan,Kiem Lien Thi Nguyen,Diem Ngoc Ngo,Thu Hien Nguyen,P. Landrieu,Laurence Colleaux,Nông Văn Hải,Lam Son Nguyen	2018	2
5	The emerging roles of MicroRNAs in autism spectrum disorders Neuroscience & Biobehavioral Reviews ·Julien Fregeac,Laurence Colleaux,Lam Son Nguyen	2016	42
6	Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology 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	2016	131
7	A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy European Journal of Human Genetics ·Lam Son Nguyen,Taiane Schneider,Marlène Rio,Sébastien Moutton,Karine Siquier-Pernet,Florine Verny,Nathalie Boddaert,Isabelle Desguerre,Arnold Munich,José Luís Rosa,Valérie Cormier‐Daire,Laurence Colleaux	2015	39
8	A conserved MADS-box phosphorylation motif regulates differentiation and mitochondrial function in skeletal, cardiac, and smooth muscle cells Cell Death and Disease ·Wajihah Mughal,Lam Son Nguyen,S Pustylnik,Simone C. da Silva Rosa,S. Piotrowski,Donald Chapman,‬Min Du,Nezeka S. Alli,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	2015	41
9	Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy Molecular Psychiatry ·G. McMichael,Matthew N. Bainbridge,Eric Haan,Mark Corbett,Alison Gardner,Suzanna Thompson,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	2015	147
10	HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain Human Molecular Genetics ·Lachlan A. Jolly,Lam Son Nguyen,Deepti Domingo,Yongsheng Sun,Simon C. Barry,Miroslava Hančárová,Pavlína Plevová,Markéta Vlčková,Markéta Havlovičová,Vera M. Kalscheuer,Claudio Graziano,Tommaso Pippucci,Elena Bonora,Zdeněk Sedláček,Jozef Gécz	2015	42
11	Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth 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	2014	100
12	Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders 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	2013	116
13	Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability Human Molecular Genetics ·Mireille Melko,Lam Son Nguyen,Marie Shaw,Lachlan A. Jolly,Barbara Bardoni,Jozef Gécz	2013	10
14	Nonsense-mediated mRNA decay: Inter-individual variability and human disease Neuroscience & Biobehavioral Reviews ·Lam Son Nguyen,Miles Wilkinson,Jozef Gécz	2013	98
15	Rare copy number variation in cerebral palsy European Journal of Human Genetics ·G. McMichael,Santhosh Girirajan,Andrés Moreno-De-Luca,Jozef Gécz,Chloé Shard,Lam Son Nguyen,Jillian Nicholl,Catherine Gibson,Eric Haan,Evan E. Eichler,Christa Lese Martin,Alastair H. MacLennan	2013	49
16	Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay European Journal of Medical Genetics ·Sally Ann Lynch,Lam Son Nguyen,Li Yen Ng,Mary Waldron,Denise McDonald,Jozef Gécz	2012	30
17	NMD‐deficient Upf3b‐null mice display behavioral and neuropathological defects The FASEB Journal ·Lulu Huang,Eleen Y. Shum,Rachid Karam,Lam Son Nguyen,Jozef Gécz,Miles Wilkinson	2012	1
18	A UPF3-mediated regulatory switch that maintains RNA surveillance Nature Structural & Molecular Biology ·Wai-Kin Chan,Angela D. Bhalla,Hervé Le Hir,Lam Son Nguyen,Lulu Huang,Jozef Gécz,Miles Wilkinson	2009	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 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,S. Blesson,Claude Moraine,Jozef Gécz,Martine Raynaud	2009	89
20	Substance P increases microvascular permeability via nitric oxide-mediated convective pathways American Journal of Physiology-Regulatory, Integrative and Comparative Physiology ·Lam Son Nguyen,Amparo C. Villablanca,James Rutledge	1995	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), RNA modifications and cancer (6 papers), Genomics and Rare Diseases (6 papers), MicroRNA in disease regulation (5 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA and protein synthesis mechanisms (3 papers) and Receptor Mechanisms and Signaling (2 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.

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