Amalia Martı́nez-Mir

2.4k citations

50 papers · 949 indexed · h-index 20

Urology top 2%
- Hair Growth and Disorders 15
Cell Biology top 5%
- Skin and Cellular Biology Research 18
Dermatology top 5%
Ophthalmology top 5%
Molecular Biology
- RNA regulation and disease 8
- Wnt/β-catenin signaling in development and cancer 8
- Retinal Development and Disorders 6
Cellular and Molecular Neuroscience
- Neuroscience and Neuropharmacology Research 5
Physiology
- Alzheimer's disease research and treatments 5
Genetics
- Genetics and Neurodevelopmental Disorders 5

Co-authors: Angela M. Christiano Abraham Zlotogorski Derek Gordon Roser Gonzàlez‐Duarte Susana Balcells Gary S. Chuang Jürg Ott Lluı̈sa Vilageliu
Cited by: Urology Cell Biology Dermatology
Journals: Journal of Neuroscience (1 paper)PLoS ONE (1 paper)The American Journal of Human Genetics (2 papers)
Partner nations: United States Spain Israel

In The Last Decade

Amalia Martı́nez-Mir

50 papers receiving 924 citations

Peers

Countries citing papers authored by Amalia Martı́nez-Mir

Since Specialization

Citations

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

Fields of papers citing papers by Amalia Martı́nez-Mir

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amalia Martı́nez-Mir. 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 Amalia Martı́nez-Mir. The network helps show where Amalia Martı́nez-Mir may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Exploring genetic testing requests, genetic alterations and clinical associations in a cohort of children with autism spectrum disorder European Child & Adolescent Psychiatry ·Nathalia Garrido‐Torres,Renata Marqués Rodríguez,María Alemany-Navarro,Javier Sánchez,Susana García-Cerro,María Irene Ayuso,Antonio González‐Meneses,Amalia Martı́nez-Mir,Miguel Ruíz-Veguilla,Benedicto Crespo‐Facorro	2024	3
2	A Neuroligin-1 mutation associated with Alzheimer’s disease produces memory and age-dependent impairments in hippocampal plasticity iScience ·Francisco Arias-Aragón,Enriqueta Tristán‐Clavijo,Irene Martínez‐Gallego,Estefanía Robles-Lanuza,Heriberto Coatl-Cuaya,Celia Martín-Cuevas,Ana C. Sánchez-Hidalgo,Antonio Rodríguez Moreno,Amalia Martı́nez-Mir,Francisco G. Scholl	2023	2
3	A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain Neuromuscular Disorders ·P. Carbonell-Corvillo,Enriqueta Tristán‐Clavijo,Macarena Cabrera‐Serrano,Emilia Servián‐Morilla,Guillermina García Martín,Liliana Villarreal-Pérez,Eloy Rivas,Estela Área-Gómez,M.I. Chamorro-Muñoz,Alejandro Gil‐Gálvez,Antonio Miranda–Vizuete,Amalia Martı́nez-Mir,Nigel G. Laing,Carmen Paradas	2018	7
4	Proteolytic Processing of Neurexins by Presenilins Sustains Synaptic Vesicle Release Journal of Neuroscience ·Emilia Servián‐Morilla,Estefanía Robles-Lanuza,Ana C. Sánchez-Hidalgo,Rafael J. Camacho-Garcia,Juan A. Paez-Gomez,Fabiola Mavillard,Carlos A. Saura,Amalia Martı́nez-Mir,Francisco G. Scholl	2017	12
5	Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses Psychiatric Genetics ·Rafael J. Camacho-Garcia,Amaia Hervás,Claudio Toma,Noemí Balmaña,Bru Cormand,Amalia Martı́nez-Mir,Francisco G. Scholl	2013	11
6	Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata The American Journal of Human Genetics ·Amalia Martı́nez-Mir,Abraham Zlotogorski,Derek Gordon,Lynn Petukhova,Jianhong Mo,T. Conrad Gilliam,Douglas Londoño,Chad Haynes,Jürg Ott,Maria Hordinsky,Krassimira Nanova,David A. Norris,Vera H. Price,Madeleine Duvic,Angela M. Christiano	2007	103
7	A recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families British Journal of Dermatology ·Gráinne M. O’Regan,Jacek M. Żurada,Amalia Martı́nez-Mir,Angela M. Christiano,Alan D. Irvine	2007	5
8	Demystification of Chester porphyria: A nonsense mutation in the porphobilinogen deaminase gene Physiological Research ·Pamela Poblete‐Gutiérrez,T. Wiederholt,Amalia Martı́nez-Mir,HF Merk,J. M. Connor,AM Christiano,Jorge Frank	2006	2
9	Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats Journal of Investigative Dermatology Symposium Proceedings ·Hisham Bazzi,Amalia Martı́nez-Mir,Ana Kljuic,Angela M. Christiano	2005	11
10	Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata Journal of the American Academy of Dermatology ·Gary S. Chuang,Amalia Martı́nez-Mir,Adam S. Geyer,Danielle E. Engler,Benjamin Gläser,Peter B. Cserhalmi‐Friedman,Derek Gordon,Liran Horev,Barbara Lukash,Eric Herman,Manuel Prieto Cid,Sarah Brenner,Marina Landau,Eli Sprecher,Maria Pilar García Muret,Angela M. Christiano,Abraham Zlotogorski	2005	31
11	Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy The American Journal of Human Genetics ·Kazuhiko Nakabayashi,Daniela Amann,Yan Ren,Ulpu Saarialho‐Kere,Nili Avidan,S. Gentles,Jeffrey R. MacDonald,Erik G. Puffenberger,Angela M. Christiano,Amalia Martı́nez-Mir,Julio C. Salas‐Alanís,Renata Rizzo,Esther Vamos,Anja Raams,Clifford Les,Eric Seboun,Nicolaas G.J. Jaspers,J. Beckmann,Charles E. Jackson,Stephen W. Scherer	2005	55
12	Familial multiple cutaneous and uterine leiomyomas associated with papillary renal cell cancer Clinical and Experimental Dermatology ·I. Chan,Terence Z. Wong,Amalia Martı́nez-Mir,Angela M. Christiano,John A. McGrath	2005	36
13	Identification of a recurrent mutation in the human hairless gene underlying atrichia with papular lesions Clinical and Experimental Dermatology ·M. Massé,Amalia Martı́nez-Mir,H. Lam,Michael T. Geraghty,Angela M. Christiano	2005	5
14	Genetic Linkage Studies in Alopecia Areata Journal of Investigative Dermatology Symposium Proceedings ·Amalia Martı́nez-Mir,Abraham Zlotogorski,Jürg Ott,Derek Gordon,Angela M. Christiano	2003	22
15	Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene Clinical and Experimental Dermatology ·M. Paradisi,Gary S. Chuang,C. Angelo,Cristina Pedicelli,Amalia Martı́nez-Mir,Angela M. Christiano	2003	11
16	Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24 Journal of Medical Genetics ·Amalia Martı́nez-Mir,Abraham Zlotogorski,Douglas Londoño,Derek Gordon,Adina Grunn,Erasmo Saucedo Uribe,Liran Horev,Irune Ruiz,Nory Omayra Dávalos,O Alayan,Jing Liu,T. Conrad Gilliam,Julio C. Salas‐Alanís,Angela M. Christiano	2003	18
17	A Recurrent Mutation in the ARS (Component B) Gene Encoding SLURP-1 in Turkish Families with Mal de Meleda: Evidence of a Founder Effect Journal of Investigative Dermatology ·Guofang Hu,Mehmet Yıldırım,Vahide Baysal,Özlem Yerebakan,Ertan Yılmaz,H. Serhat Inaloz,Amalia Martı́nez-Mir,Angela M. Christiano,Jülide Tok Çelebi	2003	9
18	Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata Journal of Investigative Dermatology ·Amalia Martı́nez-Mir,Benjamin Gläser,Gary S. Chuang,Liran Horev,Arie Waldman,Danielle E. Engler,Derek Gordon,Lynda Spelman,Ioannis Hatzibougias,Jack Green,Angela M. Christiano,Abraham Zlotogorski	2003	44
19	Analysis ofABCA4in mixed Spanish families segregating different retinal dystrophies Human Mutation ·Eva Paloma,Rosa M. Coco,Amalia Martı́nez-Mir,Lluı̈sa Vilageliu,Susana Balcells,Roser Gonzàlez‐Duarte	2002	15
20	Characterization of the amphioxus presenilin gene in a high gene-density genomic region illustrates duplication during the vertebrate lineage Gene ·Amalia Martı́nez-Mir,Cristian Cañestro,Roser Gonzàlez‐Duarte,Ricard Albalat	2001	11

About Amalia Martı́nez-Mir

Amalia Martı́nez-Mir is a scholar working on Urology, Cell Biology and Molecular Biology, having authored 50 papers that have together received 949 indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (18 papers), Hair Growth and Disorders (15 papers), RNA regulation and disease (8 papers), Wnt/β-catenin signaling in development and cancer (8 papers), Retinal Development and Disorders (6 papers), Neuroscience and Neuropharmacology Research (5 papers), Alzheimer's disease research and treatments (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Urology (256 citations), Cell Biology (278 citations) and Dermatology (119 citations). Amalia Martı́nez-Mir has collaborated with scholars based in United States, Spain and Israel. Frequent co-authors include Angela M. Christiano, Abraham Zlotogorski, Derek Gordon, Roser Gonzàlez‐Duarte, Susana Balcells, Gary S. Chuang, Jürg Ott, Lluı̈sa Vilageliu, Francisco G. Scholl and Liran Horev. Their work appears in journals such as Journal of Neuroscience, PLoS ONE 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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