Ester Margarit

1.6k total citations
32 papers, 800 citations indexed

About

Ester Margarit is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Ester Margarit has authored 32 papers receiving a total of 800 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 17 papers in Pediatrics, Perinatology and Child Health and 13 papers in Molecular Biology. Recurrent topics in Ester Margarit's work include Prenatal Screening and Diagnostics (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers) and Genomic variations and chromosomal abnormalities (11 papers). Ester Margarit is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers) and Genomic variations and chromosomal abnormalities (11 papers). Ester Margarit collaborates with scholars based in Spain, United States and Armenia. Ester Margarit's co-authors include Aurora Sánchez, Rafael Oliva, Anna Soler, Carmen Morales, A. Borrell, Francisca Ballesta, Irene Mademont‐Soler, V. Borobio, Ana Carrió and Anna Soler and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Human Reproduction and Fertility and Sterility.

In The Last Decade

Ester Margarit

32 papers receiving 682 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ester Margarit Spain 17 489 313 294 183 130 32 800
DM de Kretser Australia 9 239 0.5× 359 1.1× 131 0.4× 372 2.0× 27 0.2× 13 772
Richard H. Heller United States 12 237 0.5× 187 0.6× 60 0.2× 51 0.3× 49 0.4× 21 478
Leon A. Sheean United States 11 240 0.5× 257 0.8× 299 1.0× 327 1.8× 110 0.8× 22 814
Antoni Riera‐Escamilla Italy 13 612 1.3× 565 1.8× 164 0.6× 742 4.1× 56 0.4× 24 1.2k
Calvin Greene Canada 15 381 0.8× 212 0.7× 376 1.3× 502 2.7× 131 1.0× 25 847
Isabelle Koscinski France 13 280 0.6× 219 0.7× 74 0.3× 436 2.4× 14 0.1× 29 675
Vincent W. Aoki United States 13 362 0.7× 367 1.2× 216 0.7× 907 5.0× 22 0.2× 18 1.1k
B. Hilscher Germany 12 251 0.5× 290 0.9× 54 0.2× 418 2.3× 36 0.3× 38 654
Heinrich Rebbe Denmark 14 81 0.2× 78 0.2× 91 0.3× 399 2.2× 31 0.2× 23 559
Elena Martini Netherlands 16 367 0.8× 291 0.9× 831 2.8× 631 3.4× 117 0.9× 22 1.3k

Countries citing papers authored by Ester Margarit

Since Specialization
Citations

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

Fields of papers citing papers by Ester Margarit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ester Margarit

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

All Works

20 of 20 papers shown
1.
Soler, Anna, Célia Bádenas, Ester Margarit, et al.. (2016). A 92,XXXY Miscarriage Consecutive to a Digynic Triploid Pregnancy. Cytogenetic and Genome Research. 149(4). 258–261. 13 indexed citations
2.
Ros, Cristina, Anna Serra, Juan Balasch, Ester Margarit, & Camil Castelo‐Branco. (2014). Comparative cytogenetic analysis in two tissues with different lineage in Turner’s syndrome patients: correlation with phenotype. Gynecological Endocrinology. 30(4). 282–286. 3 indexed citations
3.
Margarit, Ester, Carmen Morales, Laia Rodríguez‐Revenga, et al.. (2012). Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability. American Journal of Medical Genetics Part A. 158A(3). 611–616. 21 indexed citations
4.
Mademont‐Soler, Irene, Carmen Morales, Jordi Bruguera, et al.. (2010). Subtelomeric MLPA: is it really useful in prenatal diagnosis?. Prenatal Diagnosis. 30(12-13). 1165–1169. 5 indexed citations
5.
Mademont‐Soler, Irene, Carmen Morales, Irene Madrigal, et al.. (2009). Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation. American Journal of Medical Genetics Part A. 149A(12). 2820–2823. 20 indexed citations
6.
Soler, Anna, Carmen Morales, Célia Bádenas, et al.. (2007). A Retrospective and Theoretical Evaluation of Rapid Methods for Detecting Chromosome Abnormalities and Their Implications on Genetic Counseling Based on a Series of 3868 CVS Diagnoses. Fetal Diagnosis and Therapy. 23(2). 126–131. 4 indexed citations
7.
Morales, Carmen, Anna Soler, Jordi Bruguera, et al.. (2007). Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion. Cytogenetic and Genome Research. 116(4). 319–323. 21 indexed citations
8.
Morales, Carmen, Aurora Sánchez, Jordi Bruguera, et al.. (2007). Cytogenetic study of spontaneous abortions using semi‐direct analysis of chorionic villi samples detects the broadest spectrum of chromosome abnormalities. American Journal of Medical Genetics Part A. 146A(1). 66–70. 62 indexed citations
9.
Morales, Carmen, Irene Madrigal, José Manuel Rodrı́guez, et al.. (2006). Duplication/deletion mosaicism of the 7q(21.1 → 31.3) region. American Journal of Medical Genetics Part A. 143A(2). 179–183. 16 indexed citations
10.
Margarit, Ester. (2005). Gene symbol: ATP7B. Disease: Wilson's disease.. PubMed. 118(3-4). 544–5. 1 indexed citations
11.
Ballescà, José Luís, et al.. (2004). High frequency of gr/gr chromosome Y deletions in consecutive oligospermic ICSI candidates. Human Reproduction. 20(1). 216–220. 84 indexed citations
12.
Margarit, Ester, et al.. (2000). SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite. American Journal of Medical Genetics. 90(1). 25–28. 25 indexed citations
13.
Costa, Durval C., A. Borrell, J. M. Jou, et al.. (1999). Assaying the granulocyte-macrophage colony-stimulating factor (GM-CSF) as a mitogen of immature cells in fetal blood cultures. Prenatal Diagnosis. 19(1). 17–20. 1 indexed citations
14.
Soler, Anna, Ester Margarit, Ana Carrió, et al.. (1999). Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements. Journal of Medical Genetics. 36(4). 333–334. 5 indexed citations
15.
Oliva, Rafael, Ester Margarit, Ana Carrió, et al.. (1998). Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injection. Fertility and Sterility. 70(3). 506–510. 72 indexed citations
16.
Costa, Dolors, A. Borrell, Anna Soler, et al.. (1998). Cytogenetic Studies in Fetal Blood. Fetal Diagnosis and Therapy. 13(3). 169–175. 3 indexed citations
17.
Margarit, Ester, Cristina Rebordosa, José Vidal, et al.. (1998). Identification of Conserved Potentially Regulatory Sequences of the SRY Gene from 10 Different Species of Mammals. Biochemical and Biophysical Research Communications. 245(2). 370–377. 43 indexed citations
18.
Borrell, A., Dolors Costa, Júlia Ojuel, et al.. (1997). Limited Effectiveness of Femur and Humerus Shortening as Markers of Down Syndrome in Early Midtrimester Fetuses. Fetal Diagnosis and Therapy. 12(3). 156–162. 3 indexed citations
19.
Margarit, Ester, et al.. (1996). Development in a 46 XX Boy with Positive SRY Gene. Journal of Pediatric Endocrinology and Metabolism. 9(6). 623–6. 12 indexed citations
20.
Costa, Dolors, A. Borrell, Ester Margarit, et al.. (1995). Rapid fetal karyotype from cystic hygroma and pleural effusions. Prenatal Diagnosis. 15(2). 141–148. 19 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.

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