Franz Binkert

2.6k citations

50 papers · 1.7k indexed · h-index 24

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics

Papers in

Pediatrics, Perinatology and Child Health 28
- Prenatal Screening and Diagnostics 28
Genetics 39
- Genomic variations and chromosomal abnormalities 28
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genetic Syndromes and Imprinting 7
- Genomics and Rare Diseases 3

Co-authors: Albert Schinzel Wendy P. Robinson Isabel Lorda‐Sánchez Stylianos E. Antonarakis Werner Schmid Michael B. Petersen Fosco Bernasconi A. Prader
Journals: European Journal of Human Genetics (5 papers)Journal of Medical Genetics (4 papers)Human Genetics (3 papers)Prenatal Diagnosis (3 papers)Human Heredity (2 papers)
Partner nations: Switzerland United States Austria

In The Last Decade

Franz Binkert

50 papers receiving 1.6k citations

Peers

Countries citing papers authored by Franz Binkert

Since Specialization

Citations

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

Fields of papers citing papers by Franz Binkert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Franz Binkert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Franz Binkert Line = papers co-authored together Franz Binkert links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Impact of prenatal diganosis on the prevalence of live births with Down sysndrome in the eastern half of Switzerland 1980-1996 Swiss Medical Weekly ·Franz Binkert, Albert Schinzel, (unknown)	2002	18
2	Parental origin and mechanisms of formation of triploidy: a study of 25 cases European Journal of Human Genetics ·Alessandra Baumer, Damina Balmer, Franz Binkert, Albert Schinzel	2000	35
3	Penoscrotal hypospadias and coarctation of the aorta with mixed gonadal dysgenesis Pediatric Surgery International ·Daniel Konrad, Roberto Sossai, Julie Besson, Franz Binkert, Sevilhan Artan, A. F. Schärli	2000	5
4	Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes European Journal of Human Genetics ·Benno Röthlisberger, Dieter Kotzot, Lukrecija Brečević, Michael Köehler, Damina Balmer, Franz Binkert, Albert Schinzel	1999	45
5	Isochromosomes 12p and 9p: parental origin and possible mechanisms of formation European Journal of Human Genetics ·Fabrizio Dutly, Damina Balmer, Alessandra Baumer, Franz Binkert, Albert Schinzel	1998	45
6	Serum parameters and nuchal translucency in first trimester screening for fetal chromosomal abnormalities BJOG An International Journal of Obstetrics & Gynaecology ·Roland Zimmermann, Sonia Robledo Ruiz, Kibar FİLİZ, Franz Binkert, Josef Achermann, Gedis Grudzinskas	1996	46
7	Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21; 21) occur postzygotically American Journal of Medical Genetics ·Jean‐Louis Blouin, Franz Binkert, Stylianos E. Antonarakis	1994	30
8	An interstitial deletion of proximal 8q (q11???q13) in a girl with Silver-russell syndrome-like features Clinical Dysmorphology ·Albert Schinzel, Wendy P. Robinson, Franz Binkert, A Fanconi	1994	35
9	Ultrasound screening for chromosomal anomalies in the first trimester of pregnancy Prenatal Diagnosis ·Kibar FİLİZ, Franz Binkert, Josef Achermann, Werner Schmid	1993	55
10	Clinical and Molecular Analysis of Five(Inv) Dup(15) Patients European Journal of Human Genetics ·Wendy P. Robinson, Franz Binkert, Fernández Llamazares Ah, T.L. Head, Wilfried Müller, W Rosenkranz, Albert Schinzel	1993	119
11	Parental origin of the supernumerary chromosome in trisomy 18 Clinical Genetics ·Susan Williams McKay, Wendy P. Robinson, Roland Spiegel, Franz Binkert, 康夫白岩, Albert Schinzel	1993	29
12	Reduced recombination and paternal age effect in Klinefelter syndrome Human Genetics ·Isabel Lorda‐Sánchez, Franz Binkert, Fina Alfiana Damayanti, Suli Dong, Hever Latisnere‐Barragán	1992	85
13	Uniparental Origin of Sex Chromosome Polysomies Human Heredity ·Isabel Lorda‐Sánchez, Franz Binkert, Kaye L. Bennett, Hans Moser, W Rosenkranz, Fina Alfiana Damayanti, Albert Schinzel	1992	19
14	Molecular study of 45,X conceptuses: Correlation with clinical findings American Journal of Medical Genetics ·Isabel Lorda‐Sánchez, Franz Binkert, Fina Alfiana Damayanti, Albert Schinzel	1992	40
15	A 48,XXY,+21 Down syndrome patient with additional paternal X and maternal 21 Human Genetics ·Isabel Lorda‐Sánchez, Michael B. Petersen, Franz Binkert, Fina Alfiana Damayanti, Werner Schmid, Bhavani Paramashivan, Stylianos E. Antonarakis, Albert Schinzel	1991	21
16	Partial Trisomy of Chromosome 18 (pter→q12) following a Familial 18;21 Translocation rcp(18;21)(q12;q11) Human Heredity ·Franz Binkert, Fahad Alahmari, Albert Schinzel	1990	10
17	Die Chorionzotten-(Plazenta-)Biopsie im II. und III. Trimenon: Neue Perspektiven der Pränataldiagnostik Geburtshilfe und Frauenheilkunde ·春恵逸見, Franz Binkert, Catherine Sam, Carrie Lau	1987	4
18	Pre-implantation embryos of chinese hamster. II. Incidence and type of karyotype anomalies after treatment of the paternal post-meiotic germ cells with an alkylating mutagen Mutation Research/Environmental Mutagenesis and Related Subjects ·Franz Binkert, Werner Schmid	1977	18
19	Pre-implantation embryos of Chinese hamster. I. Incidence of karyotype anomalies in 226 control embryos Mutation Research/Environmental Mutagenesis and Related Subjects ·Franz Binkert, Werner Schmid	1977	17
20	Types of chromosome aberration in pre-implantation embryos of Chinese hamster after treatment of the sires with Treninon Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Franz Binkert, Werner Schmid	1975	1

About Franz Binkert

Franz Binkert is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Plant Science, Clinical Biochemistry and Molecular Biology, having authored 50 papers that have together received 1.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (28 papers), Genomic variations and chromosomal abnormalities (28 papers), Chromosomal and Genetic Variations (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genetic Syndromes and Imprinting (7 papers), Genomics and Chromatin Dynamics (4 papers), Genomics and Rare Diseases (3 papers) and DNA Repair Mechanisms (3 papers). The work is most often cited by research in Genetics (1.3k citations), Pediatrics, Perinatology and Child Health (932 citations), Developmental Biology (31 citations), Plant Science (403 citations) and Reproductive Medicine (72 citations). Franz Binkert has collaborated with scholars based in Switzerland, United States and Austria. Frequent co-authors include Albert Schinzel, Wendy P. Robinson, Isabel Lorda‐Sánchez, Stylianos E. Antonarakis, Werner Schmid, Michael B. Petersen, Fosco Bernasconi, A. Prader, Armand Bottani and Marco Mächler. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Human Genetics, Prenatal Diagnosis and Human Heredity.

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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