J. Briner

2.7k total citations
75 papers, 1.9k citations indexed

About

J. Briner is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, J. Briner has authored 75 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Surgery, 21 papers in Molecular Biology and 18 papers in Genetics. Recurrent topics in J. Briner's work include Fetal and Pediatric Neurological Disorders (7 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Congenital Anomalies and Fetal Surgery (6 papers). J. Briner is often cited by papers focused on Fetal and Pediatric Neurological Disorders (7 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Congenital Anomalies and Fetal Surgery (6 papers). J. Briner collaborates with scholars based in Switzerland, Germany and United States. J. Briner's co-authors include Peter Sacher, Volker Adams, Albert Schinzel, Felix Niggli, Eugen Boltshauser, Philipp U. Heitz, Beata Bode‐Lesniewska, Robert Koesters, B Odermatt and D. Zimmermann and has published in prestigious journals such as Neurology, Gut and Radiology.

In The Last Decade

J. Briner

75 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Briner Switzerland 26 609 502 314 293 270 75 1.9k
Gleb N. Budzilovich United States 25 335 0.6× 350 0.7× 185 0.6× 325 1.1× 104 0.4× 77 2.1k
Murray Feingold United States 28 1.0k 1.7× 531 1.1× 1.2k 3.7× 204 0.7× 239 0.9× 111 2.6k
A Garner United Kingdom 31 565 0.9× 369 0.7× 254 0.8× 159 0.5× 79 0.3× 124 3.0k
Corey Raffel United States 30 1.1k 1.9× 556 1.1× 497 1.6× 263 0.9× 238 0.9× 96 3.0k
Ahmad M. Mansour Lebanon 31 825 1.4× 274 0.5× 450 1.4× 142 0.5× 112 0.4× 230 3.4k
Terry D. Allen United States 22 1.5k 2.5× 364 0.7× 129 0.4× 165 0.6× 222 0.8× 53 2.5k
Kerby C. Oberg United States 24 1.0k 1.7× 521 1.0× 489 1.6× 123 0.4× 172 0.6× 75 2.4k
Ahmad S. Teebi Canada 31 1.3k 2.2× 522 1.0× 1.3k 4.1× 226 0.8× 323 1.2× 111 3.2k
Marilyn S. Pollack United States 33 1.5k 2.5× 289 0.6× 432 1.4× 166 0.6× 250 0.9× 99 3.6k
S Shuangshotĭ Thailand 24 266 0.4× 476 0.9× 110 0.4× 370 1.3× 285 1.1× 135 2.1k

Countries citing papers authored by J. Briner

Since Specialization
Citations

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

Fields of papers citing papers by J. Briner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Briner

This figure shows the co-authorship network connecting the top 25 collaborators of J. Briner. A scholar is included among the top collaborators of J. Briner 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 J. Briner. J. Briner 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.
Koesters, Robert, David R. Betts, Mirka Schmid, et al.. (1999). Human Eukaryotic Initiation Factor EIF2C1 Gene: cDNA Sequence, Genomic Organization, Localization to Chromosomal Bands 1p34–p35, and Expression. Genomics. 61(2). 210–218. 37 indexed citations
2.
Froster, Ursula G., J. Briner, Roland Zimmermann, R. Huch, & A. Huch. (1996). Bilateral brachial amelia, facial clefts, encephalocele, orbital cyst and omphalocele: a recurrent fetal malformation pattern coming into focus. Clinical Dysmorphology. 5(2). 171–174. 5 indexed citations
4.
Hubler, M., Mark E. Haskins, S. Arnold, et al.. (1996). Mucolipidosis type II in a domestic shorthair cat. Journal of Small Animal Practice. 37(9). 435–441. 15 indexed citations
5.
Wagner, Hans-Peter, A Lüthy, Andreas Hirt, et al.. (1995). Childhood NHL in Switzerland: Incidence and Survival of 120 Study and 42 Non‐Study Patients. Medical and Pediatric Oncology. 24(5). 281–286. 46 indexed citations
6.
Meuli, Martin, et al.. (1994). Lichen Sclerosus et Atrophicus Causing Phimosis in Boys: A Prospective Study with 5-Year Followup After Complete Circumcision. The Journal of Urology. 152(3). 987–989. 63 indexed citations
7.
Weber, Rainer, Herbert Kuster, Thomas Bächi, et al.. (1992). Pulmonary and Intestinal Microsporidiosis in a Patient with the Acquired Immunodeficiency Syndrome. American Review of Respiratory Disease. 146(6). 1603–1605. 57 indexed citations
8.
Inderbitzin, Daniel, et al.. (1992). Clinical Relevance of Hirschsprung-Associated Neuronal Intestinal Dysplasia (HANID). European Journal of Pediatric Surgery. 2(3). 147–149. 31 indexed citations
9.
Borchard, F, W. Meier‐Ruge, B. Wiebecke, et al.. (1991). [Disorders of the innervation of the large intestine--classification and diagnosis. Results of a consensus conference of the Society of Gastroenteropathology 1 December 1990 in Frankfurt/Main].. PubMed. 12(3). 171–4. 70 indexed citations
10.
Giedion, A, et al.. (1991). Case report 693. Skeletal Radiology. 20(7). 534–8. 5 indexed citations
11.
Briner, J., A Giedion, & M. A. Spycher. (1991). Variation of Quantitative and Qualitative Changes of Enchondral Ossification in Heterozygous Achondroplasia. Pathology - Research and Practice. 187(2-3). 271–278. 17 indexed citations
12.
Briner, J., et al.. (1990). In situ hybridization for the detection of human parvovirus B19 nucleic acid sequences in paraffin-embedded specimens. Virchows Archiv B Cell Pathology Including Molecular Pathology. 59(1). 257–261. 10 indexed citations
13.
Hammer, Frank, et al.. (1990). Inienzephalie: Pränatale und postnatale Befunde. Geburtshilfe und Frauenheilkunde. 50(6). 491–494. 4 indexed citations
14.
Reiser, Peter J., J. Briner, & Albert Schinzel. (1990). Skeletal muscular changes in Pena-Shokeir Sequence. Journal of Perinatal Medicine. 18(4). 267–274. 3 indexed citations
15.
Martin, E., et al.. (1988). Developmental Stages of Human Brain. Journal of Computer Assisted Tomography. 12(6). 917–922. 98 indexed citations
16.
Kirkinen, Pertti, Rouven Müller, H. Baumann, et al.. (1988). Cerebral blood flow velocity waveforms in hydrocephalic fetuses. Journal of Clinical Ultrasound. 16(7). 493–498. 13 indexed citations
17.
18.
Schinzel, Albert, et al.. (1984). Prenatal ultrasonographic diagnosis of holoprosencephaly two cases of cebocephaly and two of cyclopia. Archives of Gynecology and Obstetrics. 236(1). 47–53. 6 indexed citations
19.
Reutter, F, et al.. (1980). Familial glomerulopathy with fibrillar trans membranous deposits. Kidney International. 17(6). 856. 2 indexed citations
20.
Sane, Shashikant M., et al.. (1974). Cervical cord compression in diastrophic dwarfism. The Journal of Pediatrics. 84(6). 862–865. 14 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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