Siegfried Uhlhaas

2.3k citations

37 papers · 1.4k indexed · h-index 17

Pathology and Forensic Medicine top 1%
- Genetic factors in colorectal cancer 17
Developmental Biology top 5%
Oncology top 5%
Cancer Research top 10%
- Cancer Genomics and Diagnostics 5
Gastroenterology top 10%
Clinical Biochemistry
- Metabolism and Genetic Disorders 5
Genetics
- Genomic variations and chromosomal abnormalities 5
Molecular Biology
- RNA Research and Splicing 5
- RNA modifications and cancer 3
Cell Biology
- Muscle metabolism and nutrition 3
Surgery
- Cholangiocarcinoma and Gallbladder Cancer Studies 3

Co-authors: Peter Propping Waltraut Friedl Stefan Aretz Elisabeth Mangold Constanze Pagenstecher Dietlinde Stienen Steffan Loff Reiner Caspari
Cited by: Pathology and Forensic Medicine Developmental Biology Oncology
Journals: Nucleic Acids Research (1 paper)International Journal of Cancer (1 paper)Clinica Chimica Acta (2 papers)
Partner nations: Germany China Netherlands

In The Last Decade

Siegfried Uhlhaas

37 papers receiving 1.3k citations

Peers

Countries citing papers authored by Siegfried Uhlhaas

Since Specialization

Citations

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

Fields of papers citing papers by Siegfried Uhlhaas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes Hereditary Cancer in Clinical Practice ·Jonas Henn,Isabel Spier,R. Adam,Stefanie Holzapfel,Siegfried Uhlhaas,Katrin Kayser,Guido Plotz,Sophia Peters,Stefan Aretz	2019	8
2	Deep intronicAPCmutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis Human Mutation ·Isabel Spier,Sukanya Horpaopan,Stefanie Vogt,Siegfried Uhlhaas,Monika Morak,Dietlinde Stienen,Markus Draaken,Michael Ludwig,Elke Holinski‐Feder,Markus M. Nöthen,Per Hoffmann,Stefan Aretz	2012	54
3	Analysis of Rare APC Variants at the mRNA Level Journal of Molecular Diagnostics ·Astrid Kaufmann,Stefanie Vogt,Siegfried Uhlhaas,Dietlinde Stienen,Ingo Kurth,H. Hameister,Elisabeth Mangold,Judith Kötting,Elke Kaminsky,Peter Propping,Waltraut Friedl,Stefan Aretz	2009	17
4	High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome Journal of Medical Genetics ·Stefan Aretz,Dietlinde Stienen,Siegfried Uhlhaas,M. Stolte,Mark M. Entius,Steffan Loff,Walter Back,Astrid Kaufmann,KM Keller,Stefan Blaas,Reiner Siebert,Stefanie Vogt,S Spranger,Elke Holinski‐Feder,Lone Sunde,Peter Propping,W Friedl	2007	151
5	SomaticAPCmosaicism: a frequent cause of familial adenomatous polyposis (FAP) Human Mutation ·Stefan Aretz,Dietlinde Stienen,Nicolaus Friedrichs,Susanne Stemmler,Siegfried Uhlhaas,Nils Rahner,Peter Propping,Waltraut Friedl	2007	101
6	A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification Journal of Molecular Diagnostics ·Constanze Pagenstecher,Dorothea Gadzicki,Dietlinde Stienen,Siegfried Uhlhaas,Elisabeth Mangold,Nils Rahner,Mine Arslan‐Kirchner,Peter Propping,Waltraut Friedl,Stefan Aretz	2007	7
7	May the APC gene somatic mutations in tumor tissues influence the clinical features of Chinese sporadic colorectal cancers? Acta Oncologica ·Xiaorong Liu,Xiangnian Shan,Waltraut Friedl,Siegfried Uhlhaas,Peter Propping,Jintian Li,Yaping Wang	2006	7
8	High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome Human Mutation ·Stefan Aretz,Dietlinde Stienen,Siegfried Uhlhaas,Steffan Loff,Walter Back,Constanze Pagenstecher,D. Ross McLeod,Gail E. Graham,Elisabeth Mangold,René Santer,Peter Propping,Waltraut Friedl	2005	174
9	Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations? Pediatric Blood & Cancer ·Stefan Aretz,Arend Koch,Siegfried Uhlhaas,Waltraut Friedl,Peter Propping,Dietrich von Schweinitz,Torsten Pietsch	2005	72
10	Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in theAPCgene Human Mutation ·Stefan Aretz,Siegfried Uhlhaas,Yuli Sun,Constanze Pagenstecher,Elisabeth Mangold,Reiner Caspari,Gabriela Möslein,Karsten Schulmann,Peter Propping,Waltraut Friedl	2004	89
11	Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis European Journal of Human Genetics ·Stefan Aretz,Siegfried Uhlhaas,Reiner Caspari,Elisabeth Mangold,Constanze Pagenstecher,Peter Propping,Waltraut Friedl	2003	103
12	Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers Human Genetics ·Waltraut Friedl,Siegfried Uhlhaas,Karsten Schulmann,Manfred Stolte,Steffan Loff,Walter Back,Elisabeth Mangold,Martin Stern,Hanns‐Peter Knaebel,Christian Sutter,Ruthild G. Weber,Steffen Pistorius,Bettina Burger,Peter Propping	2002	123
13	Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26 American Journal of Medical Genetics ·Reiner Caspari,Siegfried Uhlhaas,Waltraut Friedl,Michael Knapp,Peter Propping	2000	4
14	Adult syndrome allelic to limb mammary syndrome (LMS)? American Journal of Medical Genetics ·Peter Propping,Waltraut Friedl,Thomas F. Wienker,Siegfried Uhlhaas,Klaus Zerres	2000	3
15	Adult syndrome allelic to limb mammary syndrome (LMS)? American Journal of Medical Genetics ·Peter Propping,Waltraut Friedl,Thomas F. Wienker,Siegfried Uhlhaas,Klaus Zerres	2000	23
16	Frequent 4‐bp deletion in exon 9 of the SMAD4MADH4 gene in familial juvenile polyposis patients Genes Chromosomes and Cancer ·Waltraut Friedl,Roland Kruse,Siegfried Uhlhaas,Manfred Stolte,Bettina Schartmann,Klaus Keller,Matthias Jungck,Martin Stern,Steffan Loff,Walter Back,Peter Propping,Dieter E. Jenne	1999	5
17	Apolipoprotein E polymorphism influences the cerebral metabolic pattern in Alzheimer's disease Neuroscience Letters ·R. Mielke,Klaus Zerres,Siegfried Uhlhaas,Jörg Kessler,W.-D. Heiß	1998	22
18	Apolipoprotein E genotype distribution in schizophrenia Psychiatric Genetics ·Shengtao Zhu,Markus M. Nöthen,Siegfried Uhlhaas,Marcella Rietschel,Judith Körner,M. Lanczik,R. Fimmers,Peter Propping	1996	23
19	MASA syndrome: Clinical variability and linkage analysis American Journal of Medical Genetics ·Marcella Rietschel,Waltraut Friedl,Siegfried Uhlhaas,M. Neugebauer,David M. Heimann,Klaus Zerres	1991	13
20	Further RFLPs at the human tyrosine hydroxylase locus Nucleic Acids Research ·Judith Körner,Siegfried Uhlhaas,Jacques Mallet,Peter Propping,A. Gal	1988	2

About Siegfried Uhlhaas

Siegfried Uhlhaas is a scholar working on Pathology and Forensic Medicine, Developmental Biology and Clinical Biochemistry, having authored 37 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (17 papers), Metabolism and Genetic Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (5 papers), RNA Research and Splicing (5 papers), Muscle metabolism and nutrition (3 papers), RNA modifications and cancer (3 papers) and Cholangiocarcinoma and Gallbladder Cancer Studies (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (886 citations), Developmental Biology (57 citations) and Oncology (471 citations). Siegfried Uhlhaas has collaborated with scholars based in Germany, China and Netherlands. Frequent co-authors include Peter Propping, Waltraut Friedl, Stefan Aretz, Elisabeth Mangold, Constanze Pagenstecher, Dietlinde Stienen, Steffan Loff, Reiner Caspari, Walter Back and Karsten Schulmann. Their work appears in journals such as Nucleic Acids Research, International Journal of Cancer and Clinica Chimica Acta.

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