Karen M. Lower

1.9k citations

34 papers · 927 indexed · h-index 15

Co-authors: Jozef Gécz M. W. Partington Douglas R. Higgs Grant R. Sutherland J. P. Fryns Ági K. Gedeon Gillian Turner Hélène Bruyèrè
Topics: Chronic Lymphocytic Leukemia Research (10 papers)Genomics and Chromatin Dynamics (6 papers)Connexins and lens biology (5 papers)
Cited by: Genetics Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Australia United Kingdom United States

In The Last Decade

Karen M. Lower

32 papers receiving 920 citations

Peers

Countries citing papers authored by Karen M. Lower

Since Specialization

Citations

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

Fields of papers citing papers by Karen M. Lower

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karen M. Lower. 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 Karen M. Lower. The network helps show where Karen M. Lower may publish in the future.

Co-authorship network of co-authors of Karen M. Lower

This figure shows the co-authorship network connecting the top 25 collaborators of Karen M. Lower. A scholar is included among the top collaborators of Karen M. Lower 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 Karen M. Lower. Karen M. Lower 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	Brief research report: ETS-1 blockade increases ICAM-1 expression in activated human retinal endothelial cells 2024 ·SHILAP Revista de lepidopterología ·(unknown),Yuefang Ma,Binoy Appukuttan,Karen M. Lower,Amanda L. Lumsden,Michael Michael,Justine R. Smith,Liam M. Ashander	1
2	Lipid uptake in chronic lymphocytic leukemia 2021 ·Experimental Hematology ·Lauren A. Thurgood,Giles Best,(unknown),Karen M. Lower,Doug A. Brooks,Bryone J. Kuss	11
3	The Combination of Metformin and Valproic Acid Has a Greater Anti-tumoral Effect on Prostate Cancer Growth In Vivo than Either Drug Alone 2018 ·In Vivo ·(unknown),Ganessan Kichenadasse,Katherine L. Morel,Tina C. Lavranos,Sonja Klebe,Karen M. Lower,Rebecca J. Ormsby,David J. Elliot,Pamela J. Sykes	11
4	The Combination of Metformin and Valproic Acid Induces Synergistic Apoptosis in the Presence of p53 and Androgen Signaling in Prostate Cancer 2017 ·Molecular Cancer Therapeutics ·(unknown),Ganessan Kichenadasse,Lisa M. Butler,Margaret M. Centenera,Katherine L. Morel,Rebecca J. Ormsby,Michael Michael,Karen M. Lower,Pamela J. Sykes	27
5	Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract 2017 ·European Journal of Human Genetics ·Owen M. Siggs,Shari Javadiyan,Shiwani Sharma,Emmanuelle Souzeau,Karen M. Lower,Deepa Taranath,(unknown),John Pater,(unknown),Kathryn P. Burdon,Jamie E. Craig	10
6	Trisomy 12 assessment by conventional fluorescence in-situ hybridization (FISH), FISH in suspension (FISH-IS) and laser scanning cytometry (LSC) in chronic lymphocytic leukemia 2017 ·Cancer Genetics ·(unknown),Karen M. Lower,Peter J. Macardle,Bryone J. Kuss	1
7	Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome) 2017 ·BMC Medical Genetics ·Shari Javadiyan,Jamie E. Craig,Shiwani Sharma,Karen M. Lower,Theresa Casey,Eric Haan,Emmanuelle Souzeau,Kathryn P. Burdon	22
8	High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia 2017 ·G3 Genes Genomes Genetics ·Shari Javadiyan,Jamie E. Craig,Emmanuelle Souzeau,Shiwani Sharma,Karen M. Lower,David A. Mackey,Sandra E. Staffieri,James E. Elder,Deepa Taranath,(unknown),(unknown),John Pater,Theresa Casey,Alex W. Hewitt,Kathryn P. Burdon	22
9	Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract 2016 ·BMC Research Notes ·Shari Javadiyan,Jamie E. Craig,Emmanuelle Souzeau,Shiwani Sharma,Karen M. Lower,John Pater,Theresa Casey,(unknown),Kathryn P. Burdon	15
10	Generation of bivalent chromatin domains during cell fate decisions 2011 ·Epigenetics & Chromatin ·Marco De Gobbi,David Garrick,Magnus Lynch,Douglas Vernimmen,Jim R. Hughes,Nicolas Goardon,Sidinh Luc,Karen M. Lower,Jacqueline A. Sloane-Stanley,Cristina Pina,Shamit Soneji,Raffaele Renella,Tariq Enver,Stephen Taylor,Sten Eirik W. Jacobsen,Paresh Vyas,Richard J. Gibbons,Douglas R. Higgs	47
11	Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition 2009 ·Proceedings of the National Academy of Sciences ·Karen M. Lower,Jim R. Hughes,Marco De Gobbi,Shirley Henderson,Vip Viprakasit,Chris Fisher,Anne Goriely,Helena Ayyub,Jackie Sloane‐Stanley,Douglas Vernimmen,Cordelia Langford,David Garrick,Richard J. Gibbons,Douglas R. Higgs	74
12	Understanding α‐Globin Gene Regulation: Aiming to Improve the Management of Thalassemia 2005 ·Annals of the New York Academy of Sciences ·Douglas R. Higgs,David Garrick,Eduardo Anguita,Marco De Gobbi,Jim R. Hughes,Mary Muers,Douglas Vernimmen,Karen M. Lower,(unknown),Anthony Argentaro,(unknown),Richard J. Gibbons	34
13	Partial Androgen Insensitivity Syndrome and t(X;5): Are There Upstream Regulatory Elements of the Androgen Receptor Gene? 2004 ·Hormone Research in Paediatrics ·Karen M. Lower,Rajeev Kumar,Erica Woollatt,Laurent Villard,Jozef Gécz,G.R. Sutherland,David F. Callen	13
14	The clinical picture of the Börjeson–Forssman–Lehmann syndrome in males and heterozygous females with PHF6 mutations 2004 ·Clinical Genetics ·G. Turner,Karen M. Lower,(unknown),Martin B. Delatycki,AK Lampe,Matthew C. Wright,(unknown),Bronwyn Kerr,Susan Schelley,H. Eugene Hoyme,(unknown),Tjitske Kleefstra,Markus Grompe,Benjamin F. Cox,Jozef Gécz,M. W. Partington	56
15	Borjeson-Forssman-Lehmann Syndrome and Multiple Pituitary Hormone Deficiency 2003 ·Journal of Pediatric Endocrinology and Metabolism ·(unknown),AK Lampe,(unknown),(unknown),Jozef Gécz,Karen M. Lower,Marianne Wright,(unknown)	10
16	Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy 2002 ·Nature Genetics ·Petter Strømme,Marie Mangelsdorf,Marie Shaw,Karen M. Lower,M. E. Suzanne Lewis,Hélène Bruyèrè,(unknown),Ági K. Gedeon,Robyn H. Wallace,Ingrid E. Scheffer,Gillian Turner,M. W. Partington,Suzanna G.M. Frints,J. P. Fryns,Grant R. Sutherland,John C. Mulley,Jozef Gécz	317
17	Characterization ofARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for X-linked mental retardation: Mutation screening in B�rjeson-Forssman-Lehmann syndrome and MRX27 2001 ·American Journal of Medical Genetics ·Karen M. Lower,Jozef Gécz	5
18	Molecular genetics of X-linked mental retardation: a complex picture emerging 2001 ·Expert Review of Molecular Diagnostics ·Karen M. Lower,Marie Mangelsdorf,Jozef Gécz	2
19	Construction of a High-Resolution Physical and Transcription Map of Chromosome 16q24.3: A Region of Frequent Loss of Heterozygosity in Sporadic Breast Cancer 1998 ·Genomics ·S.A. Whitmore,Joanna Crawford,Sinoula Apostolou,Helen J. Eyre,Elizabeth Baker,Karen M. Lower,Chatri Settasatian,(unknown),R. Seshadri,Rachel A. Gibson,Christopher G. Mathew,Anne‐Marie Cleton‐Jansen,Anna Savoia,Jan C. Pronk,Arleen D. Auerbach,Norman A. Doggett,Grant R. Sutherland,David F. Callen	27
20	Characterization and Screening for Mutations of the Growth Arrest-Specific 11 (GAS11) andC16orf3Genes at 16q24.3 in Breast Cancer 1998 ·Genomics ·S.A. Whitmore,Chatri Settasatian,Joanna Crawford,Karen M. Lower,(unknown),R. Seshadri,Cees J. Cornelisse,Elna W. Moerland,Anne‐Marie Cleton‐Jansen,Alex J. Tipping,Christopher G. Mathew,(unknown),Anna Savoia,Peter C. Verlander,Arleen D. Auerbach,(unknown),Jan C. Pronk,Norman A. Doggett,David F. Callen	44

About Karen M. Lower

Karen M. Lower is a scholar working on Genetics, Endocrinology and Genetics, having authored 34 papers that have together received 927 indexed citations. Recurring topics across this work include Chronic Lymphocytic Leukemia Research (10 papers), Genomics and Chromatin Dynamics (6 papers) and Connexins and lens biology (5 papers). The work is most often cited by research in Genetics (400 citations), Genetics (138 citations) and Molecular Biology (625 citations). Karen M. Lower has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Jozef Gécz, M. W. Partington, Douglas R. Higgs, Grant R. Sutherland, J. P. Fryns, Ági K. Gedeon, Gillian Turner, Hélène Bruyèrè, Marie Mangelsdorf and Marie Shaw. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

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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