Ulrich Finckh

4.4k citations

66 papers · 3.0k indexed · 1 hit paper · h-index 30

Molecular Biology top 5%
Physiology top 2%
Cellular and Molecular Neuroscience top 2%
Neurology top 5%
Genetics top 10%

Co-authors: Andreas Gal Hans Rommelspacher Lutz G. Schmidt Roger M. Nitsch Michael J. Denton Govindasamy Kumaramanickavel Giuliano Binetti Sumin Gu
Topics: Alzheimer's disease research and treatments (15 papers)Neurotransmitter Receptor Influence on Behavior (10 papers)Receptor Mechanisms and Signaling (9 papers)
Cited by: Cellular and Molecular Neuroscience Ophthalmology Physiology
Journals: Nature Genetics Neurology Biological Psychiatry
Partner nations: Germany Switzerland United States

In The Last Decade

Ulrich Finckh

64 papers receiving 2.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

1997 504 citations Ulrich Finckh, Govindasamy Kumaramanickavel et al. profile →

Peers

Countries citing papers authored by Ulrich Finckh

Since Specialization

Citations

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

Fields of papers citing papers by Ulrich Finckh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrich Finckh

This figure shows the co-authorship network connecting the top 25 collaborators of Ulrich Finckh. A scholar is included among the top collaborators of Ulrich Finckh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ulrich Finckh. Ulrich Finckh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Impact of high risk thrombophilia status on recurrence among children and adults with VTE: An observational multicenter cohort study 2016 ·Blood Cells Molecules and Diseases ·(unknown),(unknown),Gili Kenet,Ulrich C. Klostermeier,(unknown),Frauke Degenhardt,Ulrich Finckh,Christine Heller,Susanne Holzhauer,Ralf Ulrich Trappe,Karim Kentouche,(unknown),Karin Kurnik,Anne Krümpel,Melchior Lauten,Daniela Manner,Rolf M. Mesters,Ralf Junker,Ulrike Nowak‐Göttl	8
2	Chronic ethanol exposure changes dopamine D2 receptor splicing during retinoic acid-induced differentiation of human SH-SY5Y cells 2010 ·Pharmacological Reports ·Catrin Wernicke,(unknown),Ulrich Finckh,Hans Rommelspacher	16
3	Understanding carbamoyl-phosphate synthetase I (CPS1) deficiency by using expression studies and structure-based analysis 2010 ·Human Mutation ·Satu Pekkala,Ana Isabel Escoms Martínez,Belén Barcelona,(unknown),Ulrich Finckh,Vicente Rubio,Javier Cervera	33
4	Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex 2008 ·Human Mutation ·Sonja Stahl,(unknown),Katrin Voß,(unknown),(unknown),Oǧuzkan Sürücü,E. Kunze,Christian Netzer,Christoph Korenke,Ulrich Finckh,Mario Habek,Zdravka Poljaković,Miriam Elbracht,Sabine Rudnik‐Schöneborn,Helmut Bertalanffy,Ulrich Sure,Ute Felbor	87
5	Spinocerebellar ataxia type 17: Report of a family with reduced penetrance of an unstable Gln49TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes 2005 ·BMC Medical Genetics ·Christine Zühlke,Andreas Dalski,E. Schwinger,Ulrich Finckh	37
6	Alzheimer disease-associated cystatin C variant undergoes impaired secretion 2003 ·Neurobiology of Disease ·Luisa Benussi,Roberta Ghidoni,(unknown),Antonella Alberici,(unknown),(unknown),Francesca Nicosia,Laura Barbiero,Laura Broglio,(unknown),Simona Signorini,Ulrich Finckh,Roger M. Nitsch,Giuliano Binetti	52
7	Decreased Proopiomelanocortin mRNA in Lymphocytes of Chronic Alcoholics After Intravenous Human Corticotropin Releasing Factor Injection 2003 ·Alcoholism Clinical and Experimental Research ·Peter Rosenberger,Eckhard Mühlbauer,Thomas Weissmüller,Hans Rommelspacher,Pranav Sinha,Klaus D. Wernecke,Ulrich Finckh,Jordan S. Rettig,Wolfgang J. Kox,Claudia Spies	4
8	Association of a CB1 Cannabinoid Receptor Gene (CNR1) polymorphism with severe alcohol dependence 2002 ·Drug and Alcohol Dependence ·Lutz G. Schmidt,Jerzy Samochowiec,Ulrich Finckh,(unknown),J Horodnicki,Sophia Brismar Wendel,Hans Rommelspacher,Margret R. Hoehe	125
9	Decoding Darkness: The Search for the Genetic Causes of Alzheimer’s Disease. 2001 ·The American Journal of Human Genetics ·Ulrich Finckh	5
10	Ethanol and Gene Expression in Brain 2001 ·Alcoholism Clinical and Experimental Research ·Izuru Matsumoto,Peter A. Wilce,(unknown),Peter R. Dodd,(unknown),Rainer Spanagel,(unknown),Gerald Wolf,(unknown),Hans Rommelspacher,Ulrich Finckh,Lutz G. Schmidt	1
11	Reply to Croes et al. 2000 ·The American Journal of Human Genetics ·Ulrich Finckh,Tomas Müller‐Thomsen,Ulrike Mann,Christian Eggers,Josef Marksteiner,Wolfgang Meins,Giuliano Binetti,Antonella Alberici,Christoph Höck,Roger M. Nitsch,Andreas Gal	0
12	Genetic Association of a Cystatin C Gene Polymorphism With Late-Onset Alzheimer Disease 2000 ·Archives of Neurology ·Ulrich Finckh	120
13	High Prevalence of Pathogenic Mutations in Patients with Early-Onset Dementia Detected by Sequence Analyses of Four Different Genes 2000 ·The American Journal of Human Genetics ·Ulrich Finckh,Tomas Müller‐Thomsen,Ulrike Mann,Christian Eggers,Josef Marksteiner,Wolfgang Meins,Giuliano Binetti,Antonella Alberici,Christoph Höck,Roger M. Nitsch,Andreas Gal	148
14	Genetic association of an ( 2-macroglobulin (Val1000lle) polymorphism and Alzheimer's disease 1998 ·Human Molecular Genetics ·(unknown),Roger M. Nitsch,Steven M. Greenberg,Ulrich Finckh,Deborah Blacker,M. Albert,G. William Rebeck,Teresa Gómez‐Isla,Anne E. Clatworthy,Giuliano Binetti,C. Hock,(unknown),Ulrike Mann,(unknown),Ulrike Beisiegel,Hannes B. Staehelin,John H. Growdon,Rudolph E. Tanzi,Bradley T. Hyman	128
15	Homozygosity Mapping of Autosomal Recessive Retinitis Pigmentosa Locus (RP22) on Chromosome 16p12.1–p12.3 1998 ·Genomics ·Ulrich Finckh,Suying Xu,Govindasamy Kumaramanickavel,Manfred Schürmann,J K Mukkadan,(unknown),Sheila John,James L. Weber,Michael J. Denton,(unknown)	15
16	Simple PCR Amplification of the Entire Glucocerebrosidase Gene (GBA) Coding Region for Diagnostic Sequence Analysis 1998 ·DNA sequence ·Ulrich Finckh,Pavel Seeman,(unknown),Arndt Rolfs	11
17	Allelic association of a dopamine transporter gene polymorphism in alcohol dependence with withdrawal seizures or delirium 1997 ·Biological Psychiatry ·Thomas Sander,Helmut Harms,Jan Podschus,Ulrich Finckh,B Nickel,Arndt Rolfs,Hans Rommelspacher,Lutz Schmidt	122
18	Lack of Allelic Association of Dopamine D1 and D2 (TaqIA) Receptor Gene Polymorphisms with Reduced Dopaminergic Sensitivity in Alcoholism 1996 ·Alcoholism Clinical and Experimental Research ·Andreas Heinz,Thomas Sander,Helmut Harms,Ulrich Finckh,Silke Kühn,Peter Dufeu,Michael Dettling,Klaus Gräf,Arndt Rolfs,Hans Rommelspacher,Lutz G. Schmidt	51
19	Dopamine D2 receptor gene (DRD2) haplotypes in Caucasians 1996 ·Gene ·Ulrich Finckh,Mario Giraldo‐Velásquez,Jörg Pelz,(unknown),Thomas Sander,Lutz G. Schmidt,Hans Rommelspacher,Arndt Rolfs	20
20	Producing single-stranded DNA probes with the Taq DNA polymerase: a high yield protocol. 1991 ·PubMed ·Ulrich Finckh,Patricia A. Lingenfelter,David Myerson	57

About Ulrich Finckh

Ulrich Finckh is a scholar working on Cellular and Molecular Neuroscience, Physiology and Internal Medicine, having authored 66 papers that have together received 3.0k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (15 papers), Neurotransmitter Receptor Influence on Behavior (10 papers) and Receptor Mechanisms and Signaling (9 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (826 citations), Ophthalmology (316 citations) and Physiology (852 citations). Ulrich Finckh has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Andreas Gal, Hans Rommelspacher, Lutz G. Schmidt, Roger M. Nitsch, Michael J. Denton, Govindasamy Kumaramanickavel, Giuliano Binetti, Sumin Gu, K. R. Murthy and Birgit Lorenz. Their work appears in journals such as Nature Genetics, Neurology and Biological Psychiatry.

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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