Chayim Schell-Apacik

574 total citations
5 papers, 208 citations indexed

About

Chayim Schell-Apacik is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Chayim Schell-Apacik has authored 5 papers receiving a total of 208 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Surgery. Recurrent topics in Chayim Schell-Apacik's work include Fetal and Pediatric Neurological Disorders (3 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Chayim Schell-Apacik is often cited by papers focused on Fetal and Pediatric Neurological Disorders (3 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Chayim Schell-Apacik collaborates with scholars based in Germany and United States. Chayim Schell-Apacik's co-authors include Birgit Ertl‐Wagner, Hubertus von Voß, Maximilian Muenke, Eva Klopocki, Uwe Heinrich, Vera M. Kalscheuer, Moritz Bihler, Arpad von Moers, Elke Holinski‐Feder and Udo Koehler and has published in prestigious journals such as Human Genetics, European Journal of Pediatrics and American Journal of Medical Genetics Part A.

In The Last Decade

Chayim Schell-Apacik

5 papers receiving 199 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chayim Schell-Apacik Germany	5	146	74	53	22	19	5	208
Marie Laure Moutard France	7	280 1.9×	114 1.5×	109 2.1×	33 1.5×	24 1.3×	7	434
Christine G. Spaeth United States	9	65 0.4×	73 1.0×	62 1.2×	22 1.0×	9 0.5×	15	250
Martha Schatz United States	6	29 0.2×	91 1.2×	56 1.1×	14 0.6×	17 0.9×	8	236
Julia Tantau France	8	68 0.5×	62 0.8×	50 0.9×	12 0.5×	34 1.8×	14	143
E. Feyereisen France	9	135 0.9×	45 0.6×	58 1.1×	11 0.5×	28 1.5×	17	289
A. M. Laverda Italy	5	52 0.4×	35 0.5×	44 0.8×	14 0.6×	10 0.5×	10	136
Ting Bai China	10	112 0.8×	101 1.4×	99 1.9×	43 2.0×	33 1.7×	29	301
Sarah Glatter Austria	10	115 0.8×	22 0.3×	32 0.6×	35 1.6×	7 0.4×	17	254
Manisha Goyal India	8	36 0.2×	46 0.6×	48 0.9×	9 0.4×	16 0.8×	43	147
Ellika Sahlin Sweden	9	82 0.6×	78 1.1×	72 1.4×	8 0.4×	26 1.4×	13	193

Countries citing papers authored by Chayim Schell-Apacik

Since Specialization

Citations

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

Fields of papers citing papers by Chayim Schell-Apacik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chayim Schell-Apacik. 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 Chayim Schell-Apacik. The network helps show where Chayim Schell-Apacik may publish in the future.

Co-authorship network of co-authors of Chayim Schell-Apacik

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

All Works

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5 of 5 papers shown

1.

Hehr, Ute, Daniel Pineda‐Alvarez, Goekhan Uyanik, et al.. (2010). Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly. Human Genetics. 127(5). 555–561. 33 indexed citations

2.

Koehler, Udo, Elke Holinski‐Feder, Birgit Ertl‐Wagner, et al.. (2009). A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum. European Journal of Pediatrics. 169(4). 463–468. 33 indexed citations

3.

Schell-Apacik, Chayim, Birgit Ertl‐Wagner, Eva Klopocki, et al.. (2008). Expanding the phenotype of alopecia–contractures–dwarfism mental retardation syndrome (ACD syndrome): description of an additional case and review of the literature. European Journal of Pediatrics. 167(9). 1057–1062. 4 indexed citations

4.

Schell-Apacik, Chayim, Moritz Bihler, Birgit Ertl‐Wagner, et al.. (2008). Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients. American Journal of Medical Genetics Part A. 146A(19). 2501–2511. 120 indexed citations

5.

Schell-Apacik, Chayim, Monika Cohen, Birgit Ertl‐Wagner, et al.. (2007). Gomez-Lopez-Hernandez syndrome (cerebello-trigeminal-dermal dysplasia): description of an additional case and review of the literature. European Journal of Pediatrics. 167(1). 123–126. 18 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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