Noa Carrera

17.0k total citations
16 papers, 227 citations indexed

About

Noa Carrera is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Noa Carrera has authored 16 papers receiving a total of 227 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Noa Carrera's work include Genetic Associations and Epidemiology (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Noa Carrera is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Noa Carrera collaborates with scholars based in Spain, United Kingdom and Chile. Noa Carrera's co-authors include Javier Costas, J.F. Martí-Massó, J. A. Obeso, Ãngel Carracedo, Miguel A. García-González, Julio Sanjuán, María Dolores Moltó, Eduardo Paz, Julio Brenlla and Mario Páramo and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Noa Carrera

16 papers receiving 218 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Noa Carrera Spain	8	72	62	53	40	40	16	227
Jiong Tao China	10	56 0.8×	57 0.9×	49 0.9×	10 0.3×	25 0.6×	25	189
Amelia A. Assareh Australia	9	95 1.3×	47 0.8×	33 0.6×	13 0.3×	9 0.2×	10	220
Abdelrahim A. Sadek Egypt	8	54 0.8×	73 1.2×	67 1.3×	12 0.3×	12 0.3×	33	228
Moran Hausman‐Kedem Israel	8	39 0.5×	30 0.5×	35 0.7×	53 1.3×	8 0.2×	30	223
Mouna Ben Djebara Tunisia	10	34 0.5×	27 0.4×	53 1.0×	51 1.3×	31 0.8×	54	331
Fabrice Colas Netherlands	4	151 2.1×	55 0.9×	38 0.7×	30 0.8×	5 0.1×	4	342
Anita Fletcher United States	10	108 1.5×	28 0.5×	14 0.3×	81 2.0×	8 0.2×	18	300
B Echenne France	10	79 1.1×	46 0.7×	12 0.2×	107 2.7×	12 0.3×	23	318
Domenico Serino Italy	9	61 0.8×	57 0.9×	30 0.6×	35 0.9×	11 0.3×	22	192
Gabriele Wohlrab Switzerland	11	85 1.2×	49 0.8×	34 0.6×	64 1.6×	13 0.3×	12	380

Countries citing papers authored by Noa Carrera

Since Specialization

Citations

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

Fields of papers citing papers by Noa Carrera

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Noa Carrera

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Carrera, Noa, et al.. (2024). HNF1B Transcription Factor: Key Regulator in Renal Physiology and Pathogenesis. International Journal of Molecular Sciences. 25(19). 10609–10609. 3 indexed citations

Carrera, Noa, et al.. (2022). Genetic Kidney Diseases (GKDs) Modeling Using Genome Editing Technologies. Cells. 11(9). 1571–1571. 6 indexed citations

Carrera, Noa, et al.. (2021). Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians. International Journal of Molecular Sciences. 22(21). 11414–11414. 20 indexed citations

García-González, Miguel A., et al.. (2020). Association of single nucleotide polymorphisms with renal cell carcinoma in Algerian population. SHILAP Revista de lepidopterología. 26(1). 5 indexed citations

Rodriguez‐Lopez, Julio A., Beatriz Sobrino, Jorge Amigo, et al.. (2017). Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples. European Archives of Psychiatry and Clinical Neuroscience. 268(6). 585–592. 7 indexed citations

Costas, Javier, Noa Carrera, Pino Alonso, et al.. (2016). Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Translational Psychiatry. 6(3). e768–e768. 45 indexed citations

Rodriguez‐Lopez, Julio A., Noa Carrera, Manuel Arrojo, et al.. (2015). An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders. Clinica Chimica Acta. 445. 34–40. 5 indexed citations

Costas, Javier, Jose Javier Suárez‐Rama, Noa Carrera, et al.. (2013). Role of DISC1 Interacting Proteins in Schizophrenia Risk from Genome‐Wide Analysis of Missense SNPs. Annals of Human Genetics. 77(6). 504–512. 21 indexed citations

Carrera, Noa, Manuel Arrojo, Eduardo Paz, et al.. (2010). Testing the antagonistic pleiotropy model of schizophrenia susceptibility by analysis of DAOA, PPP1R1B, and APOL1 genes. Psychiatry Research. 179(2). 126–129. 9 indexed citations

10.

Costas, Javier, Noa Carrera, Eduardo Domínguez, et al.. (2008). A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia. Human Genetics. 124(6). 607–613. 17 indexed citations

11.

Carrera, Noa, Julio Sanjuán, María Dolores Moltó, Ãngel Carracedo, & Javier Costas. (2008). Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(3). 369–374. 30 indexed citations

12.

Obeso, J. A., J.F. Martí-Massó, & Noa Carrera. (1980). Somatosensory evoked potentials: Abnormalities with focal brain lesions remote from the primary sensorimotor area. Electroencephalography and Clinical Neurophysiology. 49(1-2). 59–65. 33 indexed citations

13.

Obeso, J. A., et al.. (1980). Neurophysiological assessment of alpha pattern coma.. Journal of Neurology Neurosurgery & Psychiatry. 43(1). 63–67. 20 indexed citations

14.

Obeso, J. A., et al.. (1979). Somatosensory evoked potentials: abnormalities in brainstem lesions.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 19(5). 417–23. 1 indexed citations

15.

Martí-Massó, J.F., et al.. (1979). [Routes and systems involved in the origin of somatosensory evoked potentials in man].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 155(6). 435–8. 1 indexed citations

16.

Obeso, J. A., et al.. (1979). Conduction velocity through the somesthetic pathway in chronic renal failure. Journal of the Neurological Sciences. 43(3). 439–445. 4 indexed citations

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.

Explore authors with similar magnitude of impact