Jürgen Horst

4.8k citations

74 papers · 2.9k indexed · h-index 27

Genetics top 2%
- Genomic variations and chromosomal abnormalities 9
- Genetic and Kidney Cyst Diseases 8
Hematology top 5%
- Hemophilia Treatment and Research 7
- Platelet Disorders and Treatments 6
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 7
Reproductive Medicine top 5%
Molecular Biology top 5%
- Cancer-related gene regulation 9
- Renal and related cancers 8
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 6

Co-authors: Bernd Dworniczak Arseni Markoff Petra Pennekamp Boris V. Skryabin Axel Schweickert Eberhard Nieschlag Martin Blum Anja Fischer
Cited by: Genetics Hematology Clinical Biochemistry
Journals: Proceedings of the National Academy of Sciences (1 paper)Nature Medicine (1 paper)The EMBO Journal (1 paper)
Partner nations: Germany United States Bulgaria

In The Last Decade

Jürgen Horst

74 papers receiving 2.8k citations

Peers

Countries citing papers authored by Jürgen Horst

Since Specialization

Citations

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

Fields of papers citing papers by Jürgen Horst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	An in-depth analysis of the mitochondrial phylogenetic landscape of Cambodia Scientific Reports ·Anita Kloss‐Brandstätter,Monika Summerer,David Horst,Basil A. Horst,Gertraud Streiter,Julia Raschenberger,Florian Kronenberg,Torpong Sanguansermsri,Jürgen Horst,Hansi Weißensteiner	2021	9
2	Southeast Asian diversity: first insights into the complex mtDNA structure of Laos BMC Evolutionary Biology ·Martin Bodner,Bettina Zimmermann,Alexander Röck,Anita Kloss‐Brandstätter,David Horst,Basil A. Horst,Sourideth Sengchanh,Torpong Sanguansermsri,Jürgen Horst,Tanja Krämer,Peter M. Schneider,Walther Parson	2011	37
3	Haemoglobin Noah Mehmet Oeztuerk (α2 δ2143 (H21)His→Tyr: A novel δ-chain variant in the 2,3-DPG binding site Journal of Chromatography B ·Emmanuel Bissé,Christine Schaeffer‐Reiss,Agnès Hovasse,Sabine Preisler-Adams,Thomas Epting,Manfred W. Baumstark,Alain Van Dorsselaer,Jürgen Horst,Heinrich Wieland	2008	3
4	A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patients Neurogenetics ·Албена Тодорова,Bilyana Georgieva,Ivailo Tournev,Tihomir Todorov,Nadja Bogdanova,Vanio Mitev,Clemens R. Mueller,Ivo Kremensky,Jürgen Horst	2007	23
5	A common haplotype of the annexin A5 (ANXA5) gene promoter is associated with recurrent pregnancy loss Human Molecular Genetics ·Nadia Bogdanova,Jürgen Horst,Marcin Chlystun,Peter J.P. Croucher,Almut Nebel,A. Bohring,Албена Тодорова,Stefan Schreiber,Volker Gerke,Michael Krawczak,Arseni Markoff	2007	83
6	Cardiovascular characterization of Pkd2+/LacZ mice, an animal model for the autosomal dominant polycystic kidney disease type 2 (ADPKD2) International Journal of Cardiology ·Jörg Stypmann,Markus A. Engelen,Stefan Orwat,Konstantinos Bilbilis,Markus Rothenburger,Lars Eckardt,Wilhelm Haverkamp,Jürgen Horst,Bernd Dworniczak,Petra Pennekamp	2006	12
7	Novel three-break rearrangement and cryptic translocations leading to colocalization of MYC and IGH signals in B-cell acute lymphoblastic leukemia Cancer Genetics and Cytogenetics ·Joëlle Tchinda,Sarah Volpert,Wolfgang E. Berdel,Thomas Büchner,Jürgen Horst	2006	2
8	An anthropoid-specific segmental duplication on human chromosome 1q22 Genomics ·Vladimir Yu. Kuryshev,Eugene Vorobyov,Dorothea Zink,Jürgen Schmitz,Timofey S. Rozhdestvensky,Ewald Münstermann,Ute Ernst,Ruth Wellenreuther,Petra Moosmayer,Stephanie Bechtel,Ingo Schupp,Jürgen Horst,Bernhard Korn,Annemarie Poustka,Stefan Wiemann	2006	21
9	Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs The American Journal of Human Genetics ·Jan Smeıtınk,Orly Elpeleg,Hana Antonická,Heleen Diepstra,Ann Saada,P. Smits,Florin Sasarman,Gert Vriend,Jasmine Jacob‐Hirsch,Avraham Shaag,Gideon Rechavi,Brigitte Welling,Jürgen Horst,Richard J. Rodenburg,Bert van den Heuvel,Eric A. Shoubridge	2006	142
10	First report of prevalence of non‐syndromic hereditary prosopagnosia (HPA) American Journal of Medical Genetics Part A ·Ingo Kennerknecht,Thomas Grueter,Brigitte Welling,Sebastian Wentzek,Jürgen Horst,Steve Edwards,M. Grueter	2006	188
11	Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A Human Mutation ·Nadja Bogdanova,Arseni Markoff,Roswith Eisert,C. Wermes,Hartmut Pöllmann,Албена Тодорова,Marcin Chlystun,Ulrike Nowak‐Göttl,Jürgen Horst	2006	41
12	High Frequency of α-Thalassemia in the So Ethnic Group of South Laos Acta Haematologica ·Sourideth Sengchanh,Torpong Sanguansermsri,David Horst,Jürgen Horst,G. Flatz	2005	12
13	The ‘Hot Spot’ of Hb E [β26(B8)Glu→Lys] in Southeast Asia: β‐Globin Anomalies in the Lao Theung Population of Southern Laos Hemoglobin ·G. Flatz,Torpong Sanguansermsri,Sourideth Sengchanh,David Horst,Jürgen Horst	2004	18
14	Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A Human Mutation ·Nadja Bogdanova,Arseni Markoff,Hartmut Pöllmann,Ulrike Nowak‐Göttl,Roswith Eisert,Bernd Dworniczak,Antonin Eigel,Jürgen Horst	2002	13
15	Duplication Dup(1)(q32q44) Detected by Comparative Genomic Hybridization (CGH): Further Delineation of Trisomies 1q Fetal Diagnosis and Therapy ·Christine Bärtsch,Mücevher Aslan,Jutta Köhler,Peter Miny,Jürgen Horst,Wolfgang Holzgreve,Helga Rehder,Bárbara Fritz	2001	24
16	Microsatellite profiles reveal an unexpected genetic relationship between Asian populations Human Genetics ·Burkhard Rolf,Basil A. Horst,Antonin Eigel,Torpong Sanguansermsri,B. Brinkmann,Jürgen Horst	1998	11
17	Identification of four novel mutations in the factor VIII gene: Three missense mutations (E1875G, G2088S, I2185T) and a 2-bp deletion (1780delTC) Human Mutation ·Kamiab Tavassoli,Antonin Eigel,Bernd Dworniczak,Elena Valtseva,Jürgen Horst	1998	6
18	Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens Human Genetics ·Thilo Dörk,Bernd Dworniczak,C. Aulehla‐Scholz,Dagmar Wieczorek,Ingolf Böhm,A Mayerová,H. H. Seydewitz,Eberhard Nieschlag,Dieter Meschede,Jürgen Horst,Hans-Jürgen Pander,H. Sperling,Félix Ratjen,Eberhard Passarge,Jörg Schmidtke,Manfred Stuhrmann	1997	190
19	Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia Fertility and Sterility ·Manuela Simoni,Jörg Gromoll,Bernd Dworniczak,R. Claus,K. Abshagen,Axel Kamischke,Cesare Carani,Dieter Meschede,Hermann M. Behre,Jürgen Horst,Eberhard Nieschlag	1997	161
20	Phenylalanine hydroxylase gene: A novel splice mutation in intron 2 in two German and Polish families with severe phenylketonuria Human Mutation ·Marta Zygulska,Antonin Eigel,Jacek J Pietrzyk,Jürgen Horst	1993	5

About Jürgen Horst

Jürgen Horst is a scholar working on Hematology, Clinical Biochemistry and Genetics, having authored 74 papers that have together received 2.9k indexed citations. Recurring topics across this work include Cancer-related gene regulation (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Renal and related cancers (8 papers), Genetic and Kidney Cyst Diseases (8 papers), Metabolism and Genetic Disorders (7 papers), Hemophilia Treatment and Research (7 papers), Platelet Disorders and Treatments (6 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Genetics (1.1k citations), Hematology (341 citations) and Clinical Biochemistry (194 citations). Jürgen Horst has collaborated with scholars based in Germany, United States and Bulgaria. Frequent co-authors include Bernd Dworniczak, Arseni Markoff, Petra Pennekamp, Boris V. Skryabin, Bernd Dworniczak, Axel Schweickert, Eberhard Nieschlag, Martin Blum, Anja Fischer and Axel Kamischke. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Medicine and The EMBO Journal.

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