A Genĉík

494 total citations
26 papers, 364 citations indexed

About

A Genĉík is a scholar working on Ophthalmology, Genetics and Molecular Biology. According to data from OpenAlex, A Genĉík has authored 26 papers receiving a total of 364 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Ophthalmology, 8 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in A Genĉík's work include Glaucoma and retinal disorders (5 papers), BRCA gene mutations in cancer (4 papers) and Genetic factors in colorectal cancer (3 papers). A Genĉík is often cited by papers focused on Glaucoma and retinal disorders (5 papers), BRCA gene mutations in cancer (4 papers) and Genetic factors in colorectal cancer (3 papers). A Genĉík collaborates with scholars based in Switzerland, Slovakia and Germany. A Genĉík's co-authors include V. Ferák, E Signer, Raymond Tobler, William P. Weber, J. Torhorst, M Hrubisko, Nicole Bürki, Hj. Müller, Hansjakob Müller and Jürg Lütschg and has published in prestigious journals such as Journal of Medical Genetics, Breast Cancer Research and Treatment and Human Genetics.

In The Last Decade

A Genĉík

26 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A Genĉík Switzerland	9	222	150	100	64	32	26	364
Theodoros Giannopoulos United Kingdom	10	145 0.7×	72 0.5×	31 0.3×	16 0.3×	4 0.1×	24	431
Chantal Farra Lebanon	12	18 0.1×	18 0.1×	71 0.7×	127 2.0×	75 2.3×	38	341
Sun Woong Kim South Korea	11	53 0.2×	49 0.3×	36 0.4×	7 0.1×	2 0.1×	24	304
Niklas Pal Sweden	8	36 0.2×	28 0.2×	61 0.6×	17 0.3×	1 0.0×	15	210
Antonino Romanzo Italy	9	85 0.4×	20 0.1×	64 0.6×	19 0.3×	1 0.0×	18	171
Tami Shohat Israel	9	6 0.0×	17 0.1×	245 2.5×	31 0.5×	13 0.4×	15	334
Mark S. Jenkins United States	8	71 0.3×	164 1.1×	47 0.5×	5 0.1×	1 0.0×	11	385
Silvia Manfroi Italy	13	27 0.1×	3 0.0×	167 1.7×	27 0.4×	302 9.4×	34	491
Siavash Ghaderi‐Sohi Iran	10	10 0.0×	10 0.1×	91 0.9×	91 1.4×	2 0.1×	16	263
Federico De Angelis Italy	8	6 0.0×	13 0.1×	25 0.3×	14 0.2×	52 1.6×	24	241

Countries citing papers authored by A Genĉík

Since Specialization

Citations

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

Fields of papers citing papers by A Genĉík

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Genĉík

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

All Works

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20 of 20 papers shown

Bürki, Nicole, M Buser, Lyman R. Emmons, et al.. (1990). Malignancies in families of women with medullary, tubular and invasive ductal breast cancer. European Journal of Cancer and Clinical Oncology. 26(3). 295–303. 8 indexed citations

Genĉík, A. (1989). Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal-recessive inheritance and complete penetrance.. PubMed. 16. 76–115. 109 indexed citations

Bürki, Nicole, A Genĉík, J. Torhorst, William P. Weber, & Hansjakob Müller. (1987). Familial and histological analyses of 138 breast cancer patients. Breast Cancer Research and Treatment. 10(2). 159–167. 8 indexed citations

Genĉík, A, et al.. (1987). Partial 1p monosomy in a physically and mentally retarded boy.. PubMed. 35(4). 309–15. 4 indexed citations

Weber, William P., M Buser, A Genĉík, et al.. (1987). In den Familien von Ovarialkarzinompatientinnen sind Mammakarzinome bei Frauen und kolorektale Karzinome bei Männern übervertreten. Geburtshilfe und Frauenheilkunde. 47(7). 460–462. 2 indexed citations

Genĉík, A, et al.. (1987). High incidence of stomach cancer in relatives of patients with malignant lymphoproliferative disorders.. PubMed. 1. 121–5. 3 indexed citations

Genĉík, A, et al.. (1986). High Incidence of Laryngeal Carcinoma in a Swiss Family. ORL. 48(3). 162–166. 7 indexed citations

Genĉík, A, et al.. (1986). Zur Heterogenität des Mammakarzinoms. Sozial- und Präventivmedizin. 31(4-5). 221–223. 2 indexed citations

Bürki, Nicole, et al.. (1985). Familiäre Tumorkrankheiten. Erste Ergebnisse einer Erhebung über ihr Vorkommen in Basel. Sozial- und Präventivmedizin. 30(1). 28–32. 1 indexed citations

10.

Weber, William P., Melanie C. Buser, A Genĉík, et al.. (1985). [Comparison of tumor incidence in 251 first-degree relatives of 50 patients with colorectal carcinoma with those of the Basel population].. PubMed. 115(29). 1005–6. 1 indexed citations

11.

Genĉík, A, et al.. (1984). Genetic analysis of familial erythrophagocytic lymphohistiocytosis. European Journal of Pediatrics. 142(4). 248–252. 33 indexed citations

12.

Genĉík, A, et al.. (1983). Partial monosomy of chromosome 10 short arms.. Journal of Medical Genetics. 20(2). 107–111. 15 indexed citations

13.

Genĉík, A, et al.. (1982). Familial occurrence of congenital diaphragmatic defect in three families.. PubMed. 37(3). 289–93. 9 indexed citations

14.

Genĉík, A, et al.. (1982). Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation.. PubMed. 23(3). 291–8. 5 indexed citations

15.

Genĉík, A, et al.. (1982). Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset. Human Genetics. 61(3). 193–197. 81 indexed citations

16.

Ferák, V., et al.. (1982). Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect. Human Genetics. 61(3). 198–200. 11 indexed citations

17.

Genĉík, A, et al.. (1980). [Population-genetical characteristics of congenital glaucoma in Slovakia (author's transl)].. PubMed. 73(3). 295–305. 1 indexed citations

18.

Genĉík, A, et al.. (1980). Chimerism 46,XX/46,XY in a phenotypic female. Human Genetics. 55(3). 407–408. 11 indexed citations

19.

Genĉík, A, et al.. (1980). Genetic heterogeneity of congenital glaucoma. Clinical Genetics. 17(4). 241–248. 28 indexed citations

20.

Genĉík, A, et al.. (1977). [Genetic heterogenicity of hydrophthalmos].. PubMed. 33(1). 59–63. 1 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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