Robert G. Knowlton

4.4k total citations · 1 hit paper
52 papers, 3.4k citations indexed

About

Robert G. Knowlton is a scholar working on Genetics, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Robert G. Knowlton has authored 52 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 20 papers in Molecular Biology and 13 papers in Immunology and Allergy. Recurrent topics in Robert G. Knowlton's work include Connective tissue disorders research (15 papers), Cell Adhesion Molecules Research (13 papers) and Skin and Cellular Biology Research (9 papers). Robert G. Knowlton is often cited by papers focused on Connective tissue disorders research (15 papers), Cell Adhesion Molecules Research (13 papers) and Skin and Cellular Biology Research (9 papers). Robert G. Knowlton collaborates with scholars based in United States, Canada and France. Robert G. Knowlton's co-authors include Jouni Uitto, Sergio A. Jiménez, Helen Donis-Keller, Valerie A. Brown, Eric J. Weaver, Michael D. Briggs, Markku Ryynänen, James W. Schumm, Jeffrey C. Braman and Darwin J. Prockop and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Robert G. Knowlton

52 papers receiving 3.2k 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.

Cystic Fibrosis Locus Defined by a Genetically Linked Polymorphic DNA Marker

1985 356 citations Robert G. Knowlton, Valerie A. Brown et al. profile →

Peers

Countries citing papers authored by Robert G. Knowlton

Since Specialization

Citations

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

Fields of papers citing papers by Robert G. Knowlton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert G. Knowlton. 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 Robert G. Knowlton. The network helps show where Robert G. Knowlton may publish in the future.

Co-authorship network of co-authors of Robert G. Knowlton

This figure shows the co-authorship network connecting the top 25 collaborators of Robert G. Knowlton. A scholar is included among the top collaborators of Robert G. Knowlton 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 Robert G. Knowlton. Robert G. Knowlton 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	Recent Trend for Environmental Compliance Provides New Opportunities for Land and Water Use at Brownfields and Other Contaminated Sites 2002 ·SSRN Electronic Journal ·Robert G. Knowlton, (unknown)	2
2	Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia 1998 ·Human Mutation ·John Loughlin, Catherine Irven, Zehra Mustafa, Michael D. Briggs, Andrew Carr, Sally Ann Lynch, Robert G. Knowlton, (unknown), Bryan Sykes	35
3	Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum 1998 ·The American Journal of Human Genetics ·Michael D. Briggs, Geert Mortier, William G. Cole, Lily King, (unknown), Jacky Bonaventure, Lieve Nuytinck, Anne De Paepe, Jules G. Leroy, Leslie G. Biesecker, Mark Lipson, William R. Wilcox, Ralph S. Lachman, David L. Rimoin, Robert G. Knowlton, Daniel H. Cohn	136
4	Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy 1997 ·Nature Genetics ·Alan D. Irvine, Laura D. Corden, Ole Swensson, (unknown), Jonathan E. Moore, David G. Frazer, Frances J.D. Smith, Robert G. Knowlton, Enno Christophers, R. Rochels, Jouni Uitto, W.H. Irwin McLean	188
5	Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA Pooling 1997 ·Human Molecular Genetics ·Nancy C. Arbour, Joël Zlotogora, Robert G. Knowlton, S. Merin, Ada Rosenmann, Adam B. Kanis, Tatiana Rokhlina, Edwin M. Stone, Val C. Sheffield	35
6	Mutations in the Cartilage Oligomeric Matrix Protein (COMP) Gene in Pseudoachondroplasia and Multiple Epiphyseal Dysplasiaa 1996 ·Annals of the New York Academy of Sciences ·Daniel H. Cohn, Michael D. Briggs, Lily King, David L. Rimoin, William R. Wilcox, Ralph S. Lachman, Robert G. Knowlton	41
7	High-Resolution Genetic and Physical Mapping of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Mutations at Chromosome 19p13.1-p12 1995 ·Genomics ·Robert G. Knowlton, (unknown), Daniel H. Cohn, Michael D. Briggs, Susan M.G. Hoffman, Brigitte Brandriff, Anne S. Olsen	11
8	Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene 1995 ·Nature Genetics ·Michael D. Briggs, Susan M.G. Hoffman, Lily King, A. Olsen, H.W. Mohrenweiser, J. G. Leroy, Geert Mortier, David L. Rimoin, Ralph S. Lachman, (unknown), (unknown), Robert G. Knowlton, D.H. Cohn	395
9	Prenatal exclusion of stickler syndrome 1994 ·Prenatal Diagnosis ·Joël Zlotogora, Menachem Granat, Robert G. Knowlton	9
10	Exclusion of type II and type VI procollagen gene mutations in a five‐generation family with multiple epiphyseal dysplasia 1993 ·American Journal of Medical Genetics ·Eric J. Weaver, (unknown), George L. Yeh, (unknown), Ralph Oehlmann, Richard E. Rothman, Sergio A. Jiménez, Robert G. Knowlton	13
11	Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75?Cys mutation in the procollagen type II gene (COL2A1) 1993 ·Human Genetics ·Charlene J. Williams, Eileen L. Considine, Robert G. Knowlton, Antonio J. Reginato, (unknown), David A Harrison, Paul Buxton, Sergio A. Jiménez, Darwin J. Prockop	81
12	Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster. 1993 ·Journal of Clinical Investigation ·Lea Pulkkinen, Angela M. Christiano, Robert G. Knowlton, Jouni Uitto	20
13	Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene. 1992 ·Journal of Clinical Investigation ·Alain Hovnanian, Philippe Duquesnoy, C Blanchet‐Bardon, Robert G. Knowlton, Serge Amselem, Mark Lathrop, (unknown), Jouni Uitto, Michel Goossens	122
14	Bullous pemphigoid antigens (BPAGs): Identification of RFLPs in human BPAG1 and BPAG2, and exclusion as candidate genes in a large kindred with dominant epidermolysis bullosa simplex 1991 ·Genomics ·Markku Ryynänen, Robert G. Knowlton, (unknown), Daisuke Sawamura, Kehua Li, George J. Giudice, Luis A. Díaz, Jouni Uitto	5
15	Preliminary Assessment of the Impact of Conceptual Model Uncertainty on Site Performance 1990 ·University of North Texas Digital Library (University of North Texas) ·D.P. Gallegos, Phillip Isabio Pohl, (unknown), Robert G. Knowlton, (unknown)	1
16	Genetic Linkage of a Polymorphism in the Type II Procollagen Gene (COL2A1) to Primary Osteoarthritis Associated with Mild Chondrodysplasia 1990 ·New England Journal of Medicine ·Robert G. Knowlton, (unknown), Roland W. Moskowitz, Eric J. Weaver, Charles J. Malemud, Mini N. Pathria, Sergio A. Jiménez, Darwin J. Prockop	141
17	Human Nidogen: Complete Amino Acid Sequence and Structural Domains Deduced from cDNAs, and Evidence for Polymorphism of the Gene 1989 ·DNA ·(unknown), (unknown), Noreen J. Hickok, David R. Olsen, Michael Fazio, (unknown), Robert G. Knowlton, Karlheinz Mann, Rainer Deutzmann, Rupert Timpl, Jouni Uitto	43
18	An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome 1989 ·Nucleic Acids Research ·Robert G. Knowlton, (unknown), Valerie A. Brown, David C. Page, Helen Donis-Keller	48
19	A BglI polymorphism in the type VI (α3) procollagen gene [COL6A3] 1988 ·Nucleic Acids Research ·Eric J. Weaver, Mon-Li Chu, Robert G. Knowlton	7
20	Characterization of a spontaneous mutation to a beta-thalassemia allele. 1986 ·PubMed ·H H Kazazian, Stuart H. Orkin, C D Boehm, Sabra C. Goff, Sze Chuen Cesar Wong, Carol E. Dowling, Peter E. Newburger, Robert G. Knowlton, Valerie A. Brown, Helen Donis-Keller	41

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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