Susan Kenwrick

4.6k total citations
48 papers, 2.9k citations indexed

About

Susan Kenwrick is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Susan Kenwrick has authored 48 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 14 papers in Genetics. Recurrent topics in Susan Kenwrick's work include Muscle Physiology and Disorders (9 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Hereditary Neurological Disorders (6 papers). Susan Kenwrick is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Hereditary Neurological Disorders (6 papers). Susan Kenwrick collaborates with scholars based in United Kingdom, United States and Germany. Susan Kenwrick's co-authors include Monique Jouet, André Rosenthal, Jane Gitschier, Fritz G. Rathjen, Thomas Brümmendorf, Mark Patterson, Barbara Levinson, Hillary F. Massa, Barbara J. Trask and Kay E. Davies and has published in prestigious journals such as Cell, The Lancet and Nucleic Acids Research.

In The Last Decade

Susan Kenwrick

47 papers receiving 2.8k citations

Peers

Countries citing papers authored by Susan Kenwrick

Since Specialization

Citations

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

Fields of papers citing papers by Susan Kenwrick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Kenwrick

This figure shows the co-authorship network connecting the top 25 collaborators of Susan Kenwrick. A scholar is included among the top collaborators of Susan Kenwrick 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 Susan Kenwrick. Susan Kenwrick 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	Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans 2003 ·Nature Genetics ·Stephen P. Robertson, Stephen R.F. Twigg, Andrew J. Sutherland‐Smith, Valérie Biancalana, Robert J. Gorlin, Denise Horn, Susan Kenwrick, Chong Ae Kim, Éva Morava, Ruth Newbury‐Ecob, Karen Helene Ørstavik, Oliver Quarrell, Charles E. Schwartz, Deborah Shears, Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie	297
2	Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection 2001 ·American Journal of Medical Genetics ·Sourour Mansour, Hayley Woffendin, Sally G. Mitton, (unknown), (unknown), Susan Kenwrick, Victoria A. Murday	82
3	Filamin (FLN1),plexin (SEX), major palmitoylated proteinp55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2 2000 ·American Journal of Medical Genetics ·Swaroop Aradhya, (unknown), Richard A. Lewis, David L. Nelson, Teresa Esposito, Alfredo Ciccodicola, Tiziana Bardaro, Michele D’Urso, Hayley Woffendin, Susan Kenwrick, Asma Smahi, S. Heuertz, Arnold Munnich, Nina S. Heiss, Annemarie Poustka, Athar H. Chishti	3
4	Neural cell recognition molecule L1: relating biological complexity to human disease mutations 2000 ·Human Molecular Genetics ·Susan Kenwrick	217
5	Radiation Hybrid Mapping of the Genes for Tenascin-R (TNR), Phosducin (PDC), Laminin C1 (LAMC1), and TAX in 1q25–q32 1997 ·Genomics ·Hawys Williams, Melitta Schachner, Bo Wang, Susan Kenwrick	3
6	Mutations in the cell adhesion molecule LI cause mental retardation 1995 ·Trends in Neurosciences ·Eric V. Wong, Susan Kenwrick, Patrick J. Willems, Vance Lemmon	151
7	Gene analysis of L1 neural cell adhesion molecule in prenatal diagnosis of hydrocephalus 1995 ·The Lancet ·Monique Jouet, Susan Kenwrick	43
8	X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene 1994 ·Nature Genetics ·Monique Jouet, André Rosenthal, (unknown), (unknown), Roger E. Stevenson, Joan Paterson, Aı̈da Metzenberg, Victor Ionâşescu, I. Karen Temple, Susan Kenwrick	309
9	A DNA Fragment from Xq21 Replaces a Deleted Region Containing the Entire FVIII Gene in a Severe Hemophilia A Patient 1994 ·Genomics ·S Murru, (unknown), Lucia Casarino, Paolo Moi, Mariano Rocchi, Angela Loi, A Figus, (unknown), (unknown), Susan Kenwrick, (unknown), Antonio Cao, Mario Pirastu	2
10	Localization of the human TAX-1 gene to 1q32.1: a region implicated in microcephaly and Van der Woude syndrome 1993 ·Human Molecular Genetics ·Susan Kenwrick, Margaret Leversha, (unknown), Thomas Hasler, P. Sonderegger	8
11	Isolation and sequence of two genes associated with a CpG island 5′ of the factor VIII gene 1992 ·Human Molecular Genetics ·Susan Kenwrick, Barbara Levinson, Sherry Taylor, Amy Shapiro, Jane Gitschier	18
12	Sequence of the human factor VIII-associated gene is conserved in mouse 1992 ·Genomics ·Barbara Levinson, John R. Bermingham, Aı̈da Metzenberg, Susan Kenwrick, Verne M. Chapman, Jane Gitschier	25
13	Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X–linked hydrocephalus 1992 ·Nature Genetics ·André Rosenthal, Monique Jouet, Susan Kenwrick	228
14	Physical mapping distal to the DMD locus 1990 ·Genomics ·Donald R. Love, J.F. Bloomfield, Susan Kenwrick, (unknown), Kay E. Davies	13
15	A transcribed gene in an intron of the human factor VIII gene 1990 ·Genomics ·Barbara Levinson, Susan Kenwrick, (unknown), R. Glenn Hammonds, Jane Gitschier	136
16	Molecular Analysis and Diagnosis of Duchenne Muscular Dystrophy 1988 ·Journal of the Royal College of Physicians of London ·S. M. Forrest, Terry Smith, Gareth Cross, Susan Kenwrick, Sarah England, Tracey Flint, Kay E. Davies	0
17	Patterns of exon deletions in Duchenne and Becker muscular dystrophy 1988 ·Human Genetics ·Andrew Read, R. Mountford, S. M. Forrest, Susan Kenwrick, K. E. Davies, R Harris	36
18	Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome 1988 ·American Journal of Medical Genetics ·K. E. Davies, Mark Patterson, Susan Kenwrick, M.V. Bell, Howard R. Sloan, Judith A. Westman, Louis J. Elsas, John D. Mahan, John M. Optiz, James F. Reynolds	21
19	Chromosome-specific alpha satellite DNA from human chromosome 1: Hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA 1987 ·Genomics ·John S. Waye, Sharon Durfy, (unknown), Susan Kenwrick, Mark Patterson, Kay E. Davies, Huntington F. Willard	94
20	Molecular analysis of X-linked diseases. 1986 ·PubMed ·Kay E. Davies, Sarah Ball, Huw Dorkins, S. M. Forrest, Susan Kenwrick, Mark Patterson, Terry Smith, Julie M. Old, Andrew King, Rajesh V. Thakker	1

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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