Edna L. Maltby

2.9k citations

24 papers · 1.9k indexed · 1 hit paper · h-index 13

Co-authors: Kath Smith Peter W. Andrews H. D. M. Moore Paul J. Gokhale Jonathan S. Draper James A. Thomson Julie A. Johnson Lorraine F. Meisner
Topics: Genomic variations and chromosomal abnormalities (7 papers)Prenatal Screening and Diagnostics (5 papers)Pluripotent Stem Cells Research (3 papers)
Cited by: Molecular Biology Genetics
Journals: Nature Biotechnology Neurology The American Journal of Human Genetics
Partner nations: United Kingdom India United States

In The Last Decade

Edna L. Maltby

24 papers receiving 1.8k 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.

Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells

2003 759 citations Jonathan S. Draper, Kath Smith et al. Nature Biotechnology profile →

Peers

Countries citing papers authored by Edna L. Maltby

Since Specialization

Citations

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

Fields of papers citing papers by Edna L. Maltby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edna L. Maltby. 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 Edna L. Maltby. The network helps show where Edna L. Maltby may publish in the future.

Co-authorship network of co-authors of Edna L. Maltby

This figure shows the co-authorship network connecting the top 25 collaborators of Edna L. Maltby. A scholar is included among the top collaborators of Edna L. Maltby 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 Edna L. Maltby. Edna L. Maltby 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 Developments in Understanding Paediatric Barrett's Oesophagus 2010 ·Marta C. Cohen,Edna L. Maltby	1
2	Molecular Abnormalities in Pediatric Barrett Esophagus: Can We Test for Potential of Neoplastic Progression? 2010 ·Pediatric and Developmental Pathology ·Edna L. Maltby,(unknown),(unknown),Mike Thomson,(unknown),Marta C. Cohen	5
3	Adaptation to culture of human embryonic stem cells and oncogenesis in vivo 2007 ·Nature Biotechnology ·Duncan Baker,Neil J. Harrison,Edna L. Maltby,Kath Smith,H. D. M. Moore,Pamela J. Shaw,Paul R. Heath,Hazel M. Holden,Peter W. Andrews	480
4	Subtypes of oligodendroglioma defined by 1p,19q deletions, differ in the proportion of apoptotic cells but not in replication-licensed non-proliferating cells 2006 ·Acta Neuropathologica ·Stephen B. Wharton,Edna L. Maltby,David Jellinek,David T. Levy,Neil Atkey,(unknown),Darach Crimmins,Kai Stoeber,Gareth Williams	14
5	Cellular differentiation hierarchies in normal and culture-adapted human embryonic stem cells 2005 ·Human Molecular Genetics ·Tariq Enver,Shamit Soneji,Chirag Joshi,John Brown,Francisco J. Iborra,Torben Ørntoft,Thomas Thykjær,Edna L. Maltby,Kath Smith,Raed Abu Dawud,Mark Jones,Maryam Moghaddam Matin,Paul J. Gokhale,Jonathan S. Draper,Peter W. Andrews	220
6	HER2 amplification status in breast cancer: a comparison between immunohistochemical staining and fluorescence in situ hybridisation using manual and automated quantitative image analysis scoring techniques 2005 ·Journal of Clinical Pathology ·Cathy Ellis,(unknown),Terence Stephenson,Edna L. Maltby	100
7	Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cellsbreakdown → 2003 ·Nature Biotechnology ·Jonathan S. Draper,Kath Smith,Paul J. Gokhale,H. D. M. Moore,Edna L. Maltby,Julie A. Johnson,Lorraine F. Meisner,Thomas P. Zwaka,James A. Thomson,Peter W. Andrews	759
8	Elevated p53 expression in benign meningiomas protects against recurrence and may be indicative of senescence 2001 ·Neuropathology and Applied Neurobiology ·(unknown),R D Battersby,Edna L. Maltby,W. R. Timperley,Janice A. Royds	18
9	Navajo poikiloderma with cyclic neutropenia in Turkish children, clinical description and exclusion of linkage to the Rothmund Thomson RECQL4 gene 2000 ·The American Journal of Human Genetics ·Nora Shannon,Regina Regan,Edna L. Maltby,Jonathan Flint,Alan S. Rigby,(unknown),(unknown)	1
10	Meningiomas, dicentric chromosomes, gliomas, and telomerase activity 1999 ·The Journal of Pathology ·Thomas L. Carroll,Edna L. Maltby,(unknown),Janice A. Royds,W. R. Timperley,David Jellinek	18
11	Cytogenetics of Iris Melanomas: Disparity with Other Uveal Tract Melanomas 1998 ·Cancer Genetics and Cytogenetics ·Karen Sisley,Christopher Brand,M A Parsons,Edna L. Maltby,Robert C. Rees,I G Rennie	19
12	A report of a child with a deletion (9)(q34.3): a recognisable phenotype? 1997 ·Journal of Medical Genetics ·(unknown),(unknown),Edna L. Maltby,(unknown),Nick Telford,Rebecca C. Tyler	21
13	Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: clinical assessment 1996 ·Clinical Genetics ·Angela Barnicoat,(unknown),E. Boyd,Zoe Docherty,(unknown),J. L. Huret,Marissa King,Edna L. Maltby,(unknown),(unknown),(unknown),M Super,John Tolmie	11
14	Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism. 1995 ·Journal of Medical Genetics ·Daniela T. Pilz,A. Dalton,Aidan A. Long,T. Jaspan,Edna L. Maltby,Oliver Quarrell	8
15	A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities. 1993 ·Journal of Medical Genetics ·J. Richard Elliott,Edna L. Maltby,(unknown)	56
16	Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation. 1992 ·Journal of Medical Genetics ·I D Young,Jane Zuccollo,Edna L. Maltby,N J Broderick	39
17	Cytogenetic studies in 50 meningiomas 1988 ·Cancer Genetics and Cytogenetics ·Edna L. Maltby,James W. Ironside,R D Battersby	62
18	The Prospective Management of a Coexistent Hydatidiform Mole and Fetus 1987 ·Australian and New Zealand Journal of Obstetrics and Gynaecology ·Eric J. Thomas,(unknown),Edna L. Maltby,Sheila L. B. Duncan	11
19	Folate sensitive site at 10q23 and its expression as a deletion. 1987 ·Journal of Medical Genetics ·Edna L. Maltby,Sarah J. Higgins	11
20	Familial pericentric inversion (13) detected by antenatal diagnosis. 1984 ·Journal of Medical Genetics ·Edna L. Maltby	5

About Edna L. Maltby

Edna L. Maltby is a scholar working on Developmental Biology, Gastroenterology and Genetics, having authored 24 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Pluripotent Stem Cells Research (3 papers). The work is most often cited by research in Molecular Biology (1.5k citations), Genetics (199 citations) and Genetics (361 citations). Edna L. Maltby has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Kath Smith, Peter W. Andrews, H. D. M. Moore, Paul J. Gokhale, Jonathan S. Draper, James A. Thomson, Julie A. Johnson, Lorraine F. Meisner, Thomas P. Zwaka and Duncan Baker. Their work appears in journals such as Nature Biotechnology, Neurology and The American Journal of Human 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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