Barbara Weiffenbach

2.2k citations

37 papers · 1.7k indexed · h-index 24

Molecular Biology top 5%
Genetics top 10%
Cellular and Molecular Neuroscience top 5%
Cardiology and Cardiovascular Medicine top 10%
Genetics top 5%

Co-authors: Welcome Bender François Karch James E. Haber Robert C. Griggs Rabi Tawil Denise A. Figlewicz James Forrester Michael McDermott
Topics: Muscle Physiology and Disorders (13 papers)Cardiomyopathy and Myosin Studies (10 papers)Fungal and yeast genetics research (6 papers)
Cited by: Genetics Molecular Biology Cellular and Molecular Neuroscience
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Nature Genetics
Partner nations: United States Canada Japan

In The Last Decade

Barbara Weiffenbach

37 papers receiving 1.7k citations

Peers

Countries citing papers authored by Barbara Weiffenbach

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Weiffenbach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Weiffenbach

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Weiffenbach. A scholar is included among the top collaborators of Barbara Weiffenbach 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 Barbara Weiffenbach. Barbara Weiffenbach 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	Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis 1998 ·Annals of Neurology ·Rabi Tawil,Denise A. Figlewicz,Robert C. Griggs,Barbara Weiffenbach	85
2	Frequency of the variant allele CYP2D6(C) among North American Caucasian lung cancer patients and controls 1997 ·Lung Cancer ·Gail L. Shaw,Barbara Weiffenbach,Roni T. Falk,James N. Frame,Haleem J. Issaq,Donald T. Moir,Neil E. Caporaso	4
3	Evidence for anticipation and association of deletion size with severity in facioscapulohumerd muscular dystrophy 1996 ·Annals of Neurology ·Rabi Tawil,James Forrester,Robert C. Griggs,Jerry R. Mendell,John T. Kissel,Michael McDermott,Wendy King,Barbara Weiffenbach,Denise A. Figlewicz,(unknown)	146
4	The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease 1994 ·Chromosome Research ·Sara T. Winokur,Ulla Bengtsson,(unknown),Katherine D. Mathews,Barbara Weiffenbach,(unknown),(unknown),(unknown),(unknown),Michael R. Altherr,Brian C. Schutte	126
5	Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype 1994 ·Human Molecular Genetics ·Richa Saxena,(unknown),Mary V. Relling,James N. Frame,Donald T. Moir,William E. Evans,Neil E. Caporaso,Barbara Weiffenbach	81
6	YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene 1994 ·Genomics ·Barbara Weiffenbach,(unknown),S. Manning,N.S.F. Ma,Brian C. Schutte,Sara T. Winokur,Michael R. Altherr,(unknown),Vincent P. Stanton,Kazushige Yokoyama,Donald T. Moir	3
7	Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy 1993 ·Human Mutation ·Rabi Tawil,(unknown),Barbara Weiffenbach,Michael R. Altherr,Thomas E. Feasby,Robert C. Griggs	7
8	Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization 1993 ·Cytogenetic and Genome Research ·W.L. Neuman,(unknown),Michael J. Dixon,Rafael Espinosa,Yogesh Patel,Y. Nakamura,Barbara Weiffenbach,Michelle M. Le Beau	2
9	Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events 1993 ·Nature Genetics ·Barbara Weiffenbach,(unknown),(unknown),Rabi Tawil,(unknown),James Gilbert,Cisca Wijmenga,Jerry R. Mendell,Sara T. Winokur,Michael R. Altherr,(unknown),(unknown),Rune R. Frants,Jeffery M. Vance,Robert C. Griggs	47
10	Framework multipoint map of the long arm of human Chromosome 4 and telomeric localization of the gene for FSHD 1992 ·Mammalian Genome ·Barbara Weiffenbach,Rebecca G. Bagley,Kathleen Falls,(unknown),(unknown),(unknown),(unknown),Jerry R. Mendell,(unknown),(unknown),Robert C. Griggs	5
11	A genetic linkage map of human chromosome 5 with 60 RFLP loci 1991 ·Genomics ·Barbara Weiffenbach,Kathleen Falls,Angela L. Bricker,Linda Hall,jeannette mcmahon,John J. Wasmuth,Vicky L. Funanage,Helen Donis-Keller	29
12	A linkage map spanning the locus for diastrophic dysplasia (DTD) 1991 ·Genomics ·(unknown),Pertti Sistonen,Ilkka Kaitila,Barbara Weiffenbach,(unknown),Albert de la Chapelle	14
13	Genetic characterization of the APC locus involved in familial adenomatous polyposis 1991 ·Gastroenterology ·Sylviane Olschwang,Barbara Weiffenbach,Pierre Laurent‐Puig,Thomas Melot,(unknown),(unknown),Rémy Salmon,R Parc,Louise C. Strong,Yusuke Nakamura,Lemuel Herrera,Gilles Thomas	12
14	Highly polymorphic RFLP marker D4S130 (CRI-L518) maps to distal 4q 1991 ·Nucleic Acids Research ·Barbara Weiffenbach,(unknown),Rebecca G. Bagley	2
15	Fanconi anemia: Evidence for linkage heterogeneity on chromosome 20q 1991 ·Genomics ·W. Mann,V.S. Venkatraj,Robert G. Allen,(unknown),(unknown),Barbara Adler‐Brecher,(unknown),Barbara Weiffenbach,Stephanie L. Sherman,Arleen D. Auerbach	38
16	Linkage Relationships of Human Arginine Vasopressin-Neurophysin-II and Oxytocin-Neurophysin-I to Prodynorphin and Other Loci on Chromosome 20 1990 ·Molecular Endocrinology ·Marshall Summar,John A. Phillips,James F. Battey,(unknown),Kenneth K. Kídd,(unknown),Barbara Weiffenbach,Thomas C. Gravius	26
17	Homothallic Switching of Saccharomyces cerevisiae Mating Type Genes by Using a Donor Containing a Large Internal Deletion 1985 ·Molecular and Cellular Biology ·Barbara Weiffenbach,James E. Haber	5
18	Domains of cis-Interaction in the Bithorax Complex 1985 ·Cold Spring Harbor Symposia on Quantitative Biology ·Welcome Bender,Barbara Weiffenbach,François Karch,Mark Peifer	56
19	Chromosomal Rearrangements Accompanying Yeast Mating-type Switching: Evidence for a Gene-conversion Model 1981 ·Cold Spring Harbor Symposia on Quantitative Biology ·James E. Haber,Barbara Weiffenbach,David T. Rogers,John H. McCusker,Lucy B. Rowe	15
20	Mutations preventing transpositions of yeast mating type alleles 1980 ·Proceedings of the National Academy of Sciences ·James E. Haber,(unknown),(unknown),Barbara Weiffenbach,Lucy B. Rowe	27

About Barbara Weiffenbach

Barbara Weiffenbach is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics, having authored 37 papers that have together received 1.7k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (13 papers), Cardiomyopathy and Myosin Studies (10 papers) and Fungal and yeast genetics research (6 papers). The work is most often cited by research in Genetics (209 citations), Molecular Biology (1.3k citations) and Cellular and Molecular Neuroscience (312 citations). Barbara Weiffenbach has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Welcome Bender, François Karch, James E. Haber, Robert C. Griggs, Rabi Tawil, Denise A. Figlewicz, James Forrester, Michael McDermott, Katherine D. Mathews and Jerry R. Mendell. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature 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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