Albert Schinzel

23.2k citations

303 papers · 12.5k indexed · 1 hit paper · h-index 55

Impact in

Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Developmental Biology top 0.5%

Papers in

Developmental Biology 22
- Congenital limb and hand anomalies 21
Genetics 201
- Genomic variations and chromosomal abnormalities 133
- Genetic Syndromes and Imprinting 50
- Genetics and Neurodevelopmental Disorders 20

Co-authors: Wendy P. Robinson Franz Binkert Werner Schmid Alessandra Baumer David W. Smith James R. Miller Mariluce Riegel John M. Opitz
Journals: Human Genetics (29 papers)Journal of Medical Genetics (28 papers)European Journal of Human Genetics (19 papers)Prenatal Diagnosis (13 papers)Clinical Genetics (12 papers)
Partner nations: Switzerland United States Germany

In The Last Decade

Albert Schinzel

300 papers receiving 11.9k citations

Hit Papers

align trajectories log scale

Catalogue of Unbalanced Chromosome Aberrations in Man 1983 · 595 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1983 Catalogue of Unbalanced Chromosome Aberrations in Man

Peers

Countries citing papers authored by Albert Schinzel

Since Specialization

Citations

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

Fields of papers citing papers by Albert Schinzel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Albert Schinzel, 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 Albert Schinzel Line = papers co-authored together Albert Schinzel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case report Croatian Medical Journal ·Ljubica Odak, Ingeborg Barišić, Inge Håvard Rekstad, Mariluce Riegel, Albert Schinzel	2011	18
2	Clinical delineation of Giuffrè–Tsukahara syndrome: Another case with microcephaly and radio‐ulnar synostosis with apparent X‐linked semi‐dominant inheritance American Journal of Medical Genetics Part A ·Harald Gaspar, B. Laguda, Alessandra Baumer, Albert Schinzel	2008	3
3	Angelman syndrome 2005: Updated consensus for diagnostic criteria American Journal of Medical Genetics Part A ·Charles A. Williams, Arthur L. Beaudet, Jill Clayton‐Smith, Joan H.M. Knoll, L. Pierre, Laura Laan, R. Ellen Magenis, A Moncla, Albert Schinzel, Jane Summers, Joseph Wagstaff	2006	420
4	Cranio‐cerebello‐cardiac (3C) syndrome: Follow‐up study of the original patient American Journal of Medical Genetics Part A ·Andreas Zankl, Tayfun Güngör, Albert Schinzel	2003	5
5	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
6	Seven cases of Wiedemann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11 American Journal of Medical Genetics ·Fabrizio Dutly, Alessandra Baumer, Nurain Farhanah, P. Morales Blanco, 宏明下川, Gundula Hebisch, Albert Schinzel	1998	41
7	CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15 Prenatal Diagnosis ·Wendy P. Robinson, Sylvie Langlois, Simone Schuffenhauer, Bernhard Horsthemke, Ron C. Michaelis, Susan L. Christian, David H. Ledbetter, Albert Schinzel	1996	50
8	Isochromosome 18p Results from Maternal Meiosis II Nondisjunction European Journal of Human Genetics ·Dieter Kotzot, Gisela Karlsruher R., A Erster, Lukrecija Brečević, Iosif W. Lurie, Seher Başaran, Jefferson Spurlock, Andreas A. Böhmler, Claudio Castellan, 崇神山, Dilshod Zoirov, Albert Schinzel	1996	47
9	A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome Nature Genetics ·Maximilian Muenke, Maria Urzedo, Andreas Hehr, Nathaniel H. Robin, H. Wolfgang Losken, Albert Schinzel, Louise J. Pulleyn, Paul Rutland, William Reardon, Sue Malcolm, Robin M. Winter	1994	466
10	Karyotype-phenotype correlations in autosomal chromosomal aberrations. PubMed ·Albert Schinzel	1993	10
11	Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4 Nature Genetics ·Jeffrey C. Murray, Steven R. Bennett, Anne E. Kwitek, Kent W. Small, Albert Schinzel, Wallace L.M. Alward, James L. Weber, Graeme I. Bell, Kenneth H. Buetow	1992	84
12	The ulnar‐mammary syndrome: an autosomal dominant pleiotropic gene Clinical Genetics ·Albert Schinzel	1987	35
13	The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families PubMed ·Albert Schinzel, R. H. Largo	1985	4
14	Prenatal ultrasonographic diagnosis of holoprosencephaly two cases of cebocephaly and two of cyclopia Archives of Gynecology and Obstetrics ·Albert Schinzel, Kibar FİLİZ, J. Briner, Werner Schmid	1984	6
15	Mono zygotic twinning as a cause of fetal wastage Clinical Genetics ·Albert Schinzel	1980	9
16	Partial trisomy for the distal long arm of chromosome 13, 46,XY Cytogenetic and Genome Research ·Albert Schinzel, M.M. Aronson, A.E. Greene, L.L. Coriell	1979	1
17	Monozygotic twinning and structural defects The Journal of Pediatrics ·Albert Schinzel, David W. Smith, James R. Miller	1979	409
18	[Slipped capital femoral epiphyses in ten members of one family: probably autosomal dominant transmission with variable penetrance (author's transl)]. PubMed ·P. E. Ochsner, Reza Razavi, Albert Schinzel	1977	2
19	Triploidie als Ursache von Schwangerschaftsgestose im 2. Trimenon Archives of Gynecology and Obstetrics ·Albert Schinzel, Kenji Hayashi, Werner Schmid, Doris Millán Restrepo, N.G. Matviychuk, Eugen Boltshauser	1975	10
20	Structural aberrations of chromosome 18. I. The 18p-syndrome PubMed ·Albert Schinzel, Werner Schmid, Simona Mičianová, Thomas E Margo, C G D Brook, Diane Pulciani	1974	30

About Albert Schinzel

Albert Schinzel is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology, having authored 303 papers that have together received 12.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (133 papers), Prenatal Screening and Diagnostics (109 papers), Genetic Syndromes and Imprinting (50 papers), Chromosomal and Genetic Variations (41 papers), Fetal and Pediatric Neurological Disorders (21 papers), Congenital limb and hand anomalies (21 papers), Epigenetics and DNA Methylation (21 papers) and Genetics and Neurodevelopmental Disorders (20 papers). The work is most often cited by research in Genetics (8.6k citations), Developmental Biology (496 citations), Pediatrics, Perinatology and Child Health (4.1k citations), Molecular Biology (6.2k citations) and Genetics (601 citations). Albert Schinzel has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Wendy P. Robinson, Franz Binkert, Werner Schmid, Alessandra Baumer, David W. Smith, James R. Miller, Mariluce Riegel, John M. Opitz, Fosco Bernasconi and Stylianos E. Antonarakis. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, European Journal of Human Genetics, Prenatal Diagnosis and Clinical Genetics.

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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