A Giedion

3.0k citations

64 papers · 2.1k indexed · 1 hit paper · h-index 26

Impact in

Developmental Biology top 5%
Rheumatology top 2%
- Osteomyelitis and Bone Disorders Research

Papers in

Genetics 31
- Connective tissue disorders research 15
- Neurogenetic and Muscular Disorders Research 5
- Genetic Syndromes and Imprinting 4
- Congenital Ear and Nasal Anomalies 4
Developmental Biology 2

Co-authors: D Vischer W Holthusen Albert Schinzel P. Dangel Georg Eich Andrea Superti‐Furga A Prader Eugen Boltshauser
Journals: RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren (4 papers)European Journal of Pediatrics (4 papers)The Journal of Pediatrics (2 papers)American Journal of Roentgenology (2 papers)Clinical Genetics (2 papers)
Partner nations: Switzerland Germany United States

In The Last Decade

A Giedion

63 papers receiving 2.0k citations

Hit Papers

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[Subacute and chronic "symmetrical" osteomyelitis]. 1972 · 319 citations

Peers

Countries citing papers authored by A Giedion

Since Specialization

Citations

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

Fields of papers citing papers by A Giedion

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	MMP13 mutations are the cause of recessive metaphyseal dysplasia, Spahr type American Journal of Medical Genetics Part A ·Luisa Bonafé, Jinlong Liang, Maria W. Górna, Qingyan Zhang, Russia Hà-Vinh Leuchter, Belinda Campos‐Xavier, Sheila Unger, J. Beckmann, Antony Le Béchec, Brian J. Stevenson, A Giedion, Xuanzhu Liu, Giulio Superti‐Furga, Wei Wang, 健志小林, Andrea Superti‐Furga	2014	12
2	Long‐term follow‐up of four patients with langer–giedion syndrome: Clinical course and complications American Journal of Medical Genetics Part A ·Albert Schinzel, Mariluce Riegel, Alessandra Baumer, Andrea Superti‐Furga, Lília Maria de Azevedo Moreira, Tjhing Man Lie, S. IOSBE, Alyasiri E.A, A Giedion	2013	26
3	Spondyloenchondrodysplasia with spasticity, cerebral calcifications, and immune dysregulation: Clinical and radiographic delineation of a pleiotropic disorder American Journal of Medical Genetics Part A ·Raffaele Renella, E J Rutherford, Martine LeMerrer, Yasemin Alanay, Nurgün Kandemir, Georg Eich, Teresa Costa, Diana Ballhausen, Eugen Boltshauser, Luisa Bonafé, A Giedion, Sheila Unger, Andrea Superti‐Furga	2006	37
4	Homozygous Mutations in IHH Cause Acrocapitofemoral Dysplasia, an Autosomal Recessive Disorder with Cone-Shaped Epiphyses in Hands and Hips The American Journal of Human Genetics ·Jan Hellemans, Paul Coucke, A Giedion, Anne De Paepe, Peter Krämer, Frits A. Beemer, Geert Mortier	2003	103
5	RMRP gene sequence analysis confirms a cartilage‐hair hypoplasia variant with only skeletal manifestations and reveals a high density of single‐nucleotide polymorphisms Clinical Genetics ·Luisa Bonafé, Katharina Schmitt, Georg Eich, A Giedion, A Superti‐Furga	2002	61
6	Phalangeal cone-shaped epiphyses of the hand: their natural history, diagnostic sensitivity, and specificity in cartilage hair hypoplasia and the trichorhinophalangeal syndromes I and II Pediatric Radiology ·A Giedion	1998	28
7	Brachydactyly-short stature-hypertension (Bilginturan) syndrome: Report on two families American Journal of Medical Genetics ·David Chitayat, Art Grix, J. Williamson Balfe, Jacques S. Abramowicz, Kimberly M. Ryan, Chin‐To Fong, Meredith M. Silver, Devereux N. Saller, George H. Bresnick, A Giedion, Shiding Ying, D L Rimoin	1997	9
8	Heterogeneity in Schwartz-Jampel chondrodystrophic myotonia European Journal of Pediatrics ·A Giedion, Eugen Boltshauser, J. Briner, Georg Eich, G. Ulrich Exner, H Fendel, Jason W. Mitchell, B Steinmann, Jürgen W. Spranger, Andrea Superti‐Furga	1997	55
9	Metaphyseal peg in geroderma osteodysplasticum: A new genetic bone marker and a specific finding? American Journal of Medical Genetics ·Georg Eich, B Steinmann, J Hodler, G. Ulrich Exner, A Giedion	1996	5
10	A new type of a lethal osteochondrodysplasia with angel-shaped brachyphalangy Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·Rosmarie Caduff, J. Briner, A Giedion, Frank Martin	1994	2
11	The weight of the fourth dimension for the diagnosis of genetic bone disease Pediatric Radiology ·A Giedion	1994	6
12	Angel‐shaped phalango‐epiphyseal dysplasia (ASPED): Identification of a new genetic bone marker American Journal of Medical Genetics ·A Giedion, A Prader, Lewis B. Schneider, Priscila Regina de Lima Oliveira, Leonard O. Langer, A. K. Poznanski	1993	12
13	Pediatric pelvis: radiographic appearance in various congenital disorders. Radiographics ·Georg Eich, Paul Babyn, A Giedion	1992	30
14	International classification of osteochondrodysplasias European Journal of Pediatrics ·(unknown), Peter Beighton, A Giedion, Robert J. Gorlin, Judith G. Hall, Magnus Klausen, K. Kozlowski, Ralph Lachman, Leonard O. Langer, P Maroteaux, A. K. Poznanski, David L. Rimoin, D. Sillence, Jürgen W. Spranger	1992	89
15	Case report 693 Skeletal Radiology ·A Giedion, K Biedermann, J. Briner, Ilewicz Witold, M. Spycher	1991	5
16	Variation of Quantitative and Qualitative Changes of Enchondral Ossification in Heterozygous Achondroplasia Pathology - Research and Practice ·J. Briner, A Giedion, M. A. Spycher	1991	17
17	Prenatal diagnosis of Schwartz–Jampel syndrome with early manifestation Prenatal Diagnosis ·U. A. Hunziker, Kibar FİLİZ, Eugen Boltshauser, A Giedion, Albert Schinzel	1989	13
18	Craniometaphyseal dysplasia with increased bone turnover and secondary hyperparathyroidism: Therapeutic effect of calcitonin The Journal of Pediatrics ·Sergio Fanconi, Jan A. Fischer, P. Wieland, A Giedion, Eugen Boltshauser, Attila Oláh, Alex M. Landolt, A. Prader	1988	26
19	Oto-spondylo-megaepiphyseal dysplasia (OSMED). PubMed ·A Giedion, Peter Sch��ler, Barbara Sarudy, Oksana Stern, A Prader, James Sulzer, Lijun Wang	1982	32
20	Unusually mild course of beta-glucuronidase deficiency in two brothers (mucopolysaccharidosis VII). PubMed ·R Gitzelmann, Ulrich Wiesmann, M. A. Spycher, N. Herschkowitz, A Giedion	1978	5

About A Giedion

A Giedion is a scholar working on Genetics, Developmental Biology, Genetics, Urology and Anatomy, having authored 64 papers that have together received 2.1k indexed citations. Recurring topics across this work include Connective tissue disorders research (15 papers), Bone health and treatments (6 papers), Neurogenetic and Muscular Disorders Research (5 papers), RNA modifications and cancer (5 papers), Urological Disorders and Treatments (5 papers), Bone Metabolism and Diseases (4 papers), Genetic Syndromes and Imprinting (4 papers) and Congenital Ear and Nasal Anomalies (4 papers). The work is most often cited by research in Developmental Biology (76 citations), Rheumatology (479 citations), Genetics (850 citations), Genetics (161 citations) and Molecular Biology (861 citations). A Giedion has collaborated with scholars based in Switzerland, Germany and United States. Frequent co-authors include D Vischer, W Holthusen, Albert Schinzel, P. Dangel, Georg Eich, Andrea Superti‐Furga, A Prader, Eugen Boltshauser, Tullio Meloni and Luisa Bonafé. Their work appears in journals such as RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren, European Journal of Pediatrics, The Journal of Pediatrics, American Journal of Roentgenology 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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