Barbara Zoll

3.1k citations

76 papers · 1.8k indexed · 1 hit paper · h-index 22

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Genetics 32
- Genomic variations and chromosomal abnormalities 21
- Genomics and Rare Diseases 7
Pediatrics, Perinatology and Child Health 20
- Prenatal Screening and Diagnostics 14

Co-authors: Michaël Otto K. Ricker Manuela C. Koch Thomas J. Jentsch Klaus Steinmeyer Frank Lehmann‐Horn C Lorenz Karl‐Heinz Grzeschik
Journals: Human Genetics (11 papers)Clinical Genetics (6 papers)Cytogenetic and Genome Research (5 papers)Journal of Medical Genetics (4 papers)Molecular Cytogenetics (3 papers)
Partner nations: Germany United Kingdom Poland

In The Last Decade

Barbara Zoll

74 papers receiving 1.7k citations

Hit Papers

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The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia 1992 · 556 citations

Peers

Countries citing papers authored by Barbara Zoll

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Zoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	"Behinderung" im Dialog zwischen Recht und Humangenetik BiblioBoard Library Catalog (Open Research Library) ·Gunnar Duttge, Wolfgang Engel, Barbara Zoll	2014	0
2	Tectonic gene mutations in patients with Joubert syndrome European Journal of Human Genetics ·Peter Huppke, Eike Wegener, Helena Böhrer‐Rabel, Hanno J. Bolz, Barbara Zoll, Jutta Gärtner, Carsten Bergmann	2014	28
3	Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes European Journal of Medical Genetics ·Silke Pauli, Thomas M. Schmidt, Rudolf Funke, Barbara Zoll, Peter Burfeind, Ursula Dybowski, Moneef Shoukier, Iris Bartels	2012	9
4	Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p? Cytogenetic and Genome Research ·Thomas Liehr, Iris Bartels, Barbara Zoll, Elisabeth Ewers, Kristin Mrasek, Nadezda Kosyakova, Martina Merkaš, A.B. Hamid, Ferdinand von Eggeling, Nicole Posorski, Anja Weise	2010	3
5	Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation Molecular Cytogenetics ·Bernd Auber, Verena Bruemmer, Barbara Zoll, Peter Burfeind, Detlef Boehm, Thomas Liehr, Knut Brockmann, Ekkehard Wilichowski, Loukas Argyriou, Iris Bartels	2009	7
6	Impairment of gastric acid secretion and increase of embryonic lethality in <i>Foxq1-</i>deficient mice Cytogenetic and Genome Research ·W. Goering, Ibrahim M. Adham, Bastian Pasche, Jörg Männer, Matthias Ochs, Wolfgang Engel, Barbara Zoll	2008	21
7	An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype European Journal of Medical Genetics ·Iris Bartels, Heike Starke, Loukas Argyriou, Simone M. Sauter, Barbara Zoll, Thomas Liehr	2006	42
8	Manifestations of hereditary hemorrhagic telangiectasia in children and adolescents European Archives of Oto-Rhino-Laryngology ·Benedikt J. Folz, Barbara Zoll, Heiko Alfke, A Toussaint, Rolf F. Maier, Jochen A. Werner	2005	28
9	Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10 Human Mutation ·Barbara Zoll, Lars Petersen, Katrin Lange, Peter Gabriel, Christiane Kiese-Himmel, Peter Rausch, Joachim Berger, Bastian Pasche, Moritz Meins, Manfred Gross, Roswitha Berger, E. Kruse, J�rgen Kunz, Karl Sperling, Franco Laccone	2002	37
10	Isolation and Characterization of the Human Forkhead Gene FOXQ1 DNA and Cell Biology ·Annette Bieller, Bastian Pasche, Susanne Frank, Birgitta Gläser, Jürgen Kunz, Kathrin Witt, Barbara Zoll	2001	61
11	Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families Human Genetics ·Christof Meyer-Kleine, Michael Otto, Barbara Zoll, ManuelaC. Koch	1994	20
12	Determination of a fragment of the c-erbB-2 translational product p185 in serum of breast cancer patients Journal of Cancer Research and Clinical Oncology ·B. Kynast, Lutz Binder, D Marx, Barbara Zoll, Hans‐Joachim Schmoll, Michael Oellerich, A. Schauer	1993	32
13	Trisomy 13 (Patau syndrome) with an 11‐year survival Clinical Genetics ·Barbara Zoll, Johannes Wolf, D. Lensing‐Hebben, M. Pruggmayer, B. Thorpe	1993	27
14	Saethre‐Chotzen syndrome (ACS III) in four generations Clinical Genetics ·Susanne C. Niemann‐Seyde, Stefan Eber, Barbara Zoll	1991	8
15	Amplification of the c-erbB oncogene is associated with malignancy in primary tumours of neuroepithelial tissue Journal of Neurology ·Uwe Diedrich, Sabine Soja, Julianne Behnke, Barbara Zoll	1991	20
16	Carrier detection in haemophilia A by direct analysis of factor VIII gene lesions Human Genetics ·David Millar, Peter J. Green, Barbara Zoll, Vijay V. Kakkar, D.N. Cooper	1991	1
17	Prenatal diagnosis and postnatal follow‐up of a child with two de novo unrelated balanced reciprocal translocations Prenatal Diagnosis ·M. Pruggmayer, Barbara Zoll, M. Leipoldt, Ulrike Thies	1990	4
18	Paramyotonia congenita and myotonic dystrophy are not allelic disorders Cytogenetic and Genome Research ·Manuela C. Koch, H G Harley, T. Grimm, M. Sarfarazi, Berndt Müller, Barbara Zoll, Peter S. Harper	1989	1
19	Linkage relationship between retinoschisis and four marker loci Human Genetics ·G. Gellert, Jens Petersen, Michael Krawczak, Barbara Zoll	1988	14
20	Segregation of all four major fibrillar collagen genes in the Marfan syndrome. Europe PMC (PubMed Central) ·Donald Ogilvie, B P Wordsworth, L. Priestley, Raymond Dalgleish, J. Schmidtke, Barbara Zoll, Bryan Sykes	1987	34

About Barbara Zoll

Barbara Zoll is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Hematology and Molecular Biology, having authored 76 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (14 papers), Chromosomal and Genetic Variations (10 papers), Cancer-related gene regulation (7 papers), Hemophilia Treatment and Research (7 papers), Genetic Neurodegenerative Diseases (7 papers), Genomics and Rare Diseases (7 papers) and Blood Coagulation and Thrombosis Mechanisms (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (460 citations), Genetics (528 citations), Molecular Biology (1.1k citations), Cardiology and Cardiovascular Medicine (365 citations) and Genetics (164 citations). Barbara Zoll has collaborated with scholars based in Germany, United Kingdom and Poland. Frequent co-authors include Michaël Otto, K. Ricker, Manuela C. Koch, Thomas J. Jentsch, Klaus Steinmeyer, Frank Lehmann‐Horn, C Lorenz, Karl‐Heinz Grzeschik, Friedrich Wolf and Iris Bartels. Their work appears in journals such as Human Genetics, Clinical Genetics, Cytogenetic and Genome Research, Journal of Medical Genetics and Molecular Cytogenetics.

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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