Alina T. Midro
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 25
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 12
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 5
- Congenital Ear and Nasal Anomalies 4
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- Prenatal Screening and Diagnostics 19
- Reproductive Medicine top 10%
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- Glycosylation and Glycoproteins Research 3
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- Chromosomal and Genetic Variations 12
Alina T. Midro
73 papers receiving 833 citations
Peers
Comparison fields: 5 of 81
- Genetics 575
- Pediatrics, Perinatology and Child Health 244
- Cancer Research 114
- Reproductive Medicine 57
- Molecular Biology 436
Countries citing papers authored by Alina T. Midro
This map shows the geographic impact of Alina T. Midro'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 Alina T. Midro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alina T. Midro more than expected).
Fields of papers citing papers by Alina T. Midro
This network shows the impact of papers produced by Alina T. Midro. 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 Alina T. Midro. The network helps show where Alina T. Midro may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Alina T. Midro, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 1 | |
| 2 | 2020 | 7 | |
| 3 | 2019 | 4 | |
| 4 | 2015 | 13 | |
| 5 | Sprzeciw sumienia w praktyce medycznej – aspekty etyczne i prawne | 2014 | 6 |
| 6 | 2014 | 7 | |
| 7 | 2013 | 1 | |
| 8 | Zespół Retta – postępy badań nad patogenezą | 2010 | 2 |
| 9 | 2009 | 19 | |
| 10 | 2007 | 40 | |
| 11 | Simple and translation forms of monosomy 4p16.1↔ pter: quantitative syndrome definition and cytogenetic evaluation by FISH | 2007 | 1 |
| 12 | 2004 | 57 | |
| 13 | 2003 | 30 | |
| 14 | Genetyczne podłoże zespołu Retta - gen MECP2 | 2001 | 1 |
| 15 | 1998 | 55 | |
| 16 | 1998 | 39 | |
| 17 | Wplyw nosicielstwa translokacji chromosomowych wzajemnych na potomstwo czlowieka | 1997 | 0 |
| 18 | 1997 | 5 | |
| 19 | 1988 | 4 | |
| 20 | [13/14 translocation in siblings with mytonic dystrophy identified by the banding technic]. | 1975 | 1 |
About Alina T. Midro
Alina T. Midro is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 74 papers that have together received 943 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Prenatal Screening and Diagnostics (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Chromosomal and Genetic Variations (12 papers), Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital Ear and Nasal Anomalies (4 papers) and Glycosylation and Glycoproteins Research (3 papers). The work is most often cited by research in Genetics (575 citations), Pediatrics, Perinatology and Child Health (244 citations) and Cancer Research (114 citations). Alina T. Midro has collaborated with scholars based in Poland, Germany and United States. Frequent co-authors include Barbara Panasiuk, R Leśniewicz, Ewa Wiland, Maciej Kurpisz, S. Stengel‐Rutkowski, Jon Stene, Beata Stasiewicz‐Jarocka, P.H.M. Lohman, Nicolaas G.J. Jaspers and Małgorzata Z. Zdzienicka. Their work appears in journals such as Genomics, Journal of Medical Genetics and Journal of Alzheimer s Disease.
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.