Dan Diego‐Álvarez

1.0k total citations
16 papers, 509 citations indexed

About

Dan Diego‐Álvarez is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Dan Diego‐Álvarez has authored 16 papers receiving a total of 509 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Dan Diego‐Álvarez's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Parvovirus B19 Infection Studies (3 papers). Dan Diego‐Álvarez is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Parvovirus B19 Infection Studies (3 papers). Dan Diego‐Álvarez collaborates with scholars based in Spain, Canada and United States. Dan Diego‐Álvarez's co-authors include Carmen Ayuso, Isabel Lorda‐Sánchez, Marta Rodríguez de Alba, Ana Bustamante‐Aragonés, Wendy P. Robinson, Cristina González-González, Maria García‐Hoyos, Joaquín Diaz-Recasens, María José Trujillo-Tiebas and Luana Avila and has published in prestigious journals such as Annals of the New York Academy of Sciences, Human Reproduction and Investigative Ophthalmology & Visual Science.

In The Last Decade

Dan Diego‐Álvarez

16 papers receiving 458 citations

Peers

Countries citing papers authored by Dan Diego‐Álvarez

Since Specialization

Citations

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

Fields of papers citing papers by Dan Diego‐Álvarez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dan Diego‐Álvarez. 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 Dan Diego‐Álvarez. The network helps show where Dan Diego‐Álvarez may publish in the future.

Co-authorship network of co-authors of Dan Diego‐Álvarez

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	COASY related pontocerebellar hypoplasia type 12: A common Indian mutation with expansion of the phenotypic spectrum 2022 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Kausik Mandal, Ashok Khurana, Dan Diego‐Álvarez, (unknown), Renu Saxena, Shubha R. Phadke, (unknown), (unknown), (unknown), Ishwar C. Verma, Ratna Dua Puri	5
2	GLYT1 encephalopathy: Further delineation of disease phenotype and discussion of pathophysiological mechanisms 2020 ·American Journal of Medical Genetics Part A ·Irene Mademont‐Soler, (unknown), (unknown), (unknown), (unknown), (unknown), María Dolores Martínez Ruiz, Dan Diego‐Álvarez, (unknown), Josep Perapoch, María Obón	4
3	Evaluating DNA methylation and gene expression variability in the human term placenta 2010 ·Placenta ·Luana Avila, Ryan K. C. Yuen, Dan Diego‐Álvarez, Maria S. Peñaherrera, Ruiwei Jiang, Wendy P. Robinson	69
4	Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss 2010 ·Human Reproduction ·Evica Rajcan‐Separovic, Dan Diego‐Álvarez, Wendy P. Robinson, Christine Tyson, Ying Qiao, Chansonette Harvard, Chris Fawcett, Dagmar K. Kalousek, Tom Philipp, Martin J. Somerville, Mary D. Stephenson	85
5	New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma 2008 ·Journal of Cystic Fibrosis ·Ana Bustamante‐Aragonés, J. Gallego‐Merlo, María José Trujillo-Tiebas, Marta Rodríguez de Alba, Cristina González-González, G. Glóver, Dan Diego‐Álvarez, Carmen Ayuso, Carmen Viana Ramos	39
6	Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriers 2008 ·Haemophilia ·Ana Bustamante‐Aragonés, Marta Rodríguez de Alba, Cristina González-González, María José Trujillo-Tiebas, Dan Diego‐Álvarez, Elena Vallespín, (unknown), Carmen Ayuso, Carmen Viana Ramos	50
7	A small and active ring x chromosome in a female with features of Kabuki syndrome 2008 ·American Journal of Medical Genetics Part A ·Laura Rodríguez, Dan Diego‐Álvarez, Isabel Lorda‐Sánchez, (unknown), M.L. Martínez‐Fernández, (unknown), M. L. Martínez‐Frías	15
8	Early noninvasive prenatal detection of a fetal CRB1 mutation causing Leber congenital amaurosis. 2008 ·PubMed ·Ana Bustamante‐Aragonés, Elena Vallespín, Marta Rodríguez de Alba, María José Trujillo-Tiebas, Cristina González-González, Dan Diego‐Álvarez, Rosa Riveiro-Álvarez, Isabel Lorda‐Sánchez, Carmen Ayuso, Carmen Ramos	10
9	New Type of Mutations in Three Spanish Families with Choroideremia 2008 ·Investigative Ophthalmology & Visual Science ·Maria García‐Hoyos, Isabel Lorda‐Sánchez, Pilar Gómez‐Garre, Cristina Villaverde, Diego Cantalapiedra, Ana Bustamante, Dan Diego‐Álvarez, Elena Vallespín, J. Gallego‐Merlo, M.J. Trujillo, Carmen Ramos, Carmen Ayuso	19
10	MLPA as a screening method of aneuploidy and unbalanced chromosomal rearrangements in spontaneous miscarriages 2007 ·Prenatal Diagnosis ·Dan Diego‐Álvarez, Marta Rodríguez de Alba, (unknown), Joaquín Diaz-Recasens, Carmen Ayuso, Carmen Ramos, Isabel Lorda‐Sánchez	46
11	Detection of a Paternally Inherited Fetal Mutation in Maternal Plasma by the Use of Automated Sequencing 2006 ·Annals of the New York Academy of Sciences ·Ana Bustamante‐Aragonés, Maria García‐Hoyos, Marta Rodríguez de Alba, Cristina González-González, Isabel Lorda‐Sánchez, Dan Diego‐Álvarez, María José Trujillo-Tiebas, Carmen Ayuso, Carmen Viana Ramos	9
12	Clinical presentation of a variant of Axenfeld–Rieger syndrome associated with subtelomeric 6p deletion 2006 ·European Journal of Medical Genetics ·Víctor Martínez‐Glez, Isabel Lorda‐Sánchez, José M. Ramı́rez, (unknown), Marta Rodríguez de Alba, Dan Diego‐Álvarez, Carmen Ramos, Charles Searby, Darryl Nishimura, Carmen Ayuso	24
13	Trisomy 2 due to a 3:1 segregation in an abortion studied by QF‐PCR and CGH 2005 ·Prenatal Diagnosis ·Isabel Lorda‐Sánchez, Dan Diego‐Álvarez, Carmen Ayuso, Marta Rodríguez de Alba, M.J. Trujillo, Carmen Ramos	18
14	Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach 2005 ·Human Reproduction ·Dan Diego‐Álvarez, (unknown), Maria García‐Hoyos, Ana Bustamante‐Aragonés, Diego Cantalapiedra, Joaquín Diaz-Recasens, (unknown), Carmen Ayuso, Isabel Lorda‐Sánchez	65
15	Application of quantitative fluorescent PCR with short tandem repeat markers to the study of aneuploidies in spontaneous miscarriages 2005 ·Human Reproduction ·Dan Diego‐Álvarez, Maria García‐Hoyos, M.J. Trujillo, Cristina González-González, Marta Rodríguez de Alba, Carmen Ayuso, (unknown), Isabel Lorda‐Sánchez	45
16	New approach for the refinement of the location of the X‐chromosome breakpoint in a previously described female patient with choroideremia carrying a X;4 translocation 2005 ·American Journal of Medical Genetics Part A ·(unknown), Raúl Sanz, Dan Diego‐Álvarez, Isabel Lorda‐Sánchez, María José Trujillo-Tiebas, Diego Cantalapiedra, Carmen Ramos, Carmen Ayuso	6

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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