Alina T. Midro

2.3k citations
74 papers · 943 indexed · h-index 16
Topics
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)

In The Last Decade

Alina T. Midro

73 papers receiving 833 citations

Peers

Alina T. Midro
Comparison fields: 5 of 81
  • Genetics 575
  • Molecular Biology 436
  • Pediatrics, Perinatology and Child Health 244
  • Plant Science 192
  • Cancer Research 114
Replace Evica Rajcan‐Separovic with:
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György Kosztolányi Hungary
Violetta Anastasiadou Cyprus
Jacob A. Reiss United States
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Alina T. Midro relative to Evica Rajcan‐Separovic Canada Evica Rajcan‐Separovic's profile →
Citations per field
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Evica Rajcan‐Separovic · 1×
Citations per year

Countries citing papers authored by Alina T. Midro

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Alina T. Midro

This figure shows the co-authorship network connecting the top 25 collaborators of Alina T. Midro. A scholar is included among the top collaborators of Alina T. Midro 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 Alina T. Midro. Alina T. Midro 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
#WorkIndexed citations
1 1
2 7
3 4
4 13
5
Sprzeciw sumienia w praktyce medycznej – aspekty etyczne i prawne
6
6 7
7 1
8
Zespół Retta – postępy badań nad patogenezą
2
9 19
10 40
11
Simple and translation forms of monosomy 4p16.1↔ pter: quantitative syndrome definition and cytogenetic evaluation by FISH
1
12 57
13 30
14
Genetyczne podłoże zespołu Retta - gen MECP2
1
15 55
16 39
17
Wplyw nosicielstwa translokacji chromosomowych wzajemnych na potomstwo czlowieka
0
18 5
19 4
20
[13/14 translocation in siblings with mytonic dystrophy identified by the banding technic].
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) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 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.

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