Judith Armstrong

3.6k citations

77 papers · 2.0k indexed · h-index 25

Impact in

Clinical Psychology top 2%
- Child Abuse and Trauma
- Personality Disorders and Psychopathology
- Psychotherapy Techniques and Applications
- Child and Adolescent Psychosocial and Emotional Development
Applied Psychology top 5%
- Psychological Testing and Assessment

Papers in

Genetics 37
- Genetics and Neurodevelopmental Disorders 29
- Genomic variations and chromosomal abnormalities 8
Developmental Biology 2

Co-authors: Richard J. Loewenstein Eve B. Carlson Frank W. Putnam Steven R. Smith David M. Roth Bethany L. Brand Joyanna L. Silberg Lita Furby
Journals: International Journal of Molecular Sciences (9 papers)The Journal of Nervous and Mental Disease (4 papers)International Journal of Eating Disorders (3 papers)Scientific Reports (2 papers)European Journal of Medical Genetics (2 papers)
Partner nations: Spain United States Portugal

In The Last Decade

Judith Armstrong

74 papers receiving 1.9k citations

Peers

Countries citing papers authored by Judith Armstrong

Since Specialization

Citations

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

Fields of papers citing papers by Judith Armstrong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	NEAT1-mediated regulation of proteostasis and mRNA localization impacts autophagy dysregulation in Rett syndrome Nucleic Acids Research ·Edilene Siqueira Soares, Eva María Chasing Vilela, Tsiropoulos, Marta Soler, A. Zhamba, Fernando Setién, Cristina Oliveira-Mateos, Helen Davidson, Kirkland Pd, Judith Armstrong, Manel Esteller, Fuwang Wei, Artur Llobet, Sònia Guil	2025	2
2	Multi‐omics in MECP2 duplication syndrome patients and carriers European Journal of Neuroscience ·S Mali Sawanta, Н.В. Блюхтерова, Қ.Қ. Макангали, Ghorbanian Morteza, Holger Prokisch, Judith Armstrong	2024	3
3	MECP2 Duplication Syndrome: AI-Based Diagnosis, Severity Scale Development and Correlation with Clinical and Molecular Variables Diagnostics ·伸亜河内, Dídac Casas‐Alba, L Morrow Ivor, Lingna Mao, Patricia Rubio, Ana García‐García, Óscar García-García, Mar O’Callaghan, S Mali Sawanta, Judith Armstrong, (unknown), (unknown)	2024	0
4	Global Impairment of Immediate-Early Genes Expression in Rett Syndrome Models and Patients Linked to Myelination Defects International Journal of Molecular Sciences ·Paolo Petazzi, M.B. Tonjes, Antonio Gómez, Iolanda Scognamiglio, Jordi Serra-Musach, Angelika Merkel, Chenglong Zou, Н.В. Блюхтерова, Mar O’Callaghan, Judith Armstrong, Manel Esteller, Sònia Guil	2023	8
5	Cognitive stimulation has potential for brain activation in individuals with Rett syndrome Journal of Intellectual Disability Research ·Zachary Daniel Bellay, Dominique Rouy, Alejandro Bachiller, Timothy Anders, Joan Francesc Alonso, Anna López‐Sala, Judith Armstrong, 陈淑慧, M. Pineda, Miguel Ángel Mañanas, Sergio Romero, Àngels García‐Cazorla	2021	8
6	Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome International Journal of Molecular Sciences ·Sofía Gouveia, M.E. Vázquez-Mosquera, Emiliano González‐Vioque, Á. Hermida Ameijeiras, A. Campoy, Judith Armstrong, 钮忠波, Liesbeth T. Wintjes, 梁伟波, Richard J. Rodenburg, María L. Couce	2021	9
7	IFT144 and mild retinitis pigmentosa in Mainzer-Saldino syndrome: A new association European Journal of Medical Genetics ·Tao Wang, Jaume Català‐Mora, A. Madrid, Judith Armstrong, Sergi Serrano, Juliana Fernandes Lorenzoni	2020	7
8	Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism Scientific Reports ·Abdul Sattar Shariq, AYİTER Nurşin, Margaret King-Schumacher, Novianus Kristian, Elisenda Cortès‐Saladelafont, Federico Ramos, D. I. Usanina, С.И. Хромов, Huafeng Zhou, N. Ganapathy, María L. Couce, Cristina Sierra, Aída Ormazábal, 典昭浜田, Rafael Artuch, Judith Armstrong, Soledad Alcántara, Àngels García‐Cazorla	2019	6
9	Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype Human Genetics ·Umberto Pera, Enrique Vidal, Silvia M. Vidal, Mauricio Sáez, Laura M. Roa, Dori Huertas, Mercè Pineda, Esther Dalfó, Joaquı́n Dopazo, Paola Jurado, Judith Armstrong, Manel Esteller	2016	48
10	Hypotonic male infant and MCT8 deficiency - a diagnosis to think about BMC Pediatrics ·Virginie Charette, Juntao He, C. Ortez, A. Nascimento, Beatriz Morte, Abdul Aziz AlSaman, Judith Armstrong, J. Colomer	2014	16
11	Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders Orphanet Journal of Rare Diseases ·Ana Fernández‐Marmiesse, B. Liu, Mercè Pineda, Jesús Manuel Eirís Puñal, María L. Couce, Manuel Castro‐Gago, José M. Fraga, Lúcia Lacerda, Sofía Gouveia, María Pérez-Poyato, Judith Armstrong, Daisy Castiñeiras, José A. Cocho	2014	38
12	Abnormal Expression of Cerebrospinal Fluid Cation Chloride Cotransporters in Patients with Rett Syndrome PLoS ONE ·Sofia Duarte, Judith Armstrong, صابرين زيتوني, C. Ortez, Ana Paula da Silva Perez, María del Mar O’Callaghan, Antonina Pereira, Francesc Sanmartí, Aída Ormazábal, Rafael Artuch, Mercédes Pineda, Àngels García‐Cazorla	2013	63
13	CDKL5 in different atypical Rett syndrome variants: Description of the first eight patients from Spain А.П. Козлова, Judith Armstrong, Muhammad Agung Frananta, Carmen Fons, Jaume Campistol, Mercè Pineda	2012	7
14	De novo Interstitial Triplication of <i>MECP2</i> in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation Cytogenetic and Genome Research ·Sonia Mayo, Sandra Monfort, Mónica Rosello, Carmen Orellana, Silvestre Oltra, Judith Armstrong, Vicenç Català, Francisco Martı́nez	2011	19
15	InterRett, a model for international data collection in a rare genetic disorder Research in autism spectrum disorders ·Umal Nour Al-Nakib, Sue Fyfe, Ami Bebbington, Nadia Bahi‐Buisson, Alison Anderson, Mercè Pineda, Alan K. Percy, Bruria Ben Zeev, Cihan Unsal, Xinhua Bao, P. Mac Leod, Judith Armstrong, Helen Leonard	2009	45
16	Novel FOXG1 mutations associated with the congenital variant of Rett syndrome Journal of Medical Genetics ·Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso, Barbara Oureilidis-DeVivo, Roberta De Filippis, Nadia Bahi‐Buisson, Juliette Nectoux, Duff Hart-Davis, Thierry Bienvenu, A. Moncla, B. Chabrol, Laurent Villard, Zita Krūmiņa, Judith Armstrong, صابرين زيتوني, M. Pineda, Eva Gak, Francesca Mari, Francesca Ariani, Alessandra Renieri	2009	74
17	The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients Gene ·Floriana Della Ragione, А. А. Тиунова, Marcella Vacca, Maria Strazzullo, Eva González‐Roca, Judith Armstrong, Vishnu Priya Sahu, Anderson da Silva Sampaio, Mercè Pineda, Maj Hultén, Eugènia Monrós, Maurizio D’Esposito, Egor Prokhortchouk	2006	9
18	Psychological Assessment of Patients with Dissociative Identity Disorder Psychiatric Clinics of North America ·Bethany L. Brand, Judith Armstrong, Richard J. Loewenstein	2006	50
19	Giant SCA8 alleles in nine children whose mother has two moderately large ones Annals of Neurology ·Jordi Corral, David Genı́s, Isabel Banchs, Zaruwa M. Zira, Judith Armstrong, Vı́ctor Volpini	2005	12
20	Characteristics of Patients with Multiple Personality and Dissociative Disorders on Psychological Testing The Journal of Nervous and Mental Disease ·Judith Armstrong, Richard J. Loewenstein	1990	135

About Judith Armstrong

Judith Armstrong is a scholar working on Genetics, Developmental Biology, Clinical Biochemistry, Clinical Psychology and Applied Psychology, having authored 77 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (29 papers), Autism Spectrum Disorder Research (14 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA modifications and cancer (7 papers), Metabolism and Genetic Disorders (6 papers), Epigenetics and DNA Methylation (6 papers), Psychotherapy Techniques and Applications (6 papers) and Mitochondrial Function and Pathology (5 papers). The work is most often cited by research in Clinical Psychology (838 citations), Applied Psychology (173 citations), Psychiatry and Mental health (359 citations), Genetics (542 citations) and Anatomy (23 citations). Judith Armstrong has collaborated with scholars based in Spain, United States and Portugal. Frequent co-authors include Richard J. Loewenstein, Eve B. Carlson, Frank W. Putnam, Steven R. Smith, David M. Roth, Bethany L. Brand, Joyanna L. Silberg, Lita Furby, Mercè Pineda and David L. Roth. Their work appears in journals such as International Journal of Molecular Sciences, The Journal of Nervous and Mental Disease, International Journal of Eating Disorders, Scientific Reports and European 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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