Nigel P. Carter

46.5k citations

98 papers · 14.1k indexed · 5 hit papers · h-index 50

Impact in

Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Aging top 0.5%

Papers in

Genetics 74
- Genomic variations and chromosomal abnormalities 65
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 7
Plant Science 38
- Chromosomal and Genetic Variations 37

Co-authors: Heike Fiegler Philippa Carr Alan Tunnacliffe Bruce A.J. Ponder Matthew E. Hurles Stephen P. Jackson Fabrizio d’Adda di Fagagna Gabriele Saretzki
Journals: Nature Genetics (9 papers)The American Journal of Human Genetics (6 papers)Genes Chromosomes and Cancer (5 papers)Human Genetics (5 papers)Chromosome Research (5 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Nigel P. Carter

98 papers receiving 13.7k citations

Hit Papers

5 papers align trajectories log scale

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources 2009 · 1.2k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2009 The American Journal of Human Genetics
2007 Nature Genetics
2006 Genome Research
2003 Nature
1992 Genomics

Peers

Countries citing papers authored by Nigel P. Carter

Since Specialization

Citations

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

Fields of papers citing papers by Nigel P. Carter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nigel P. Carter. 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 Nigel P. Carter. The network helps show where Nigel P. Carter may publish in the future.

Co-authors

The 25 scholars most cited alongside Nigel P. Carter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nigel P. Carter Line = papers co-authored together Nigel P. Carter links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Sites of Differential DNA Methylation between Placenta and Peripheral Blood American Journal Of Pathology ·Elisavet A. Papageorgiou, Heike Fiegler, Vardhman K. Rakyan, Stephan Beck, Maj Hultén, Klea Lamnissou, Nigel P. Carter, Philippos C. Patsalis	2009	91
2	Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart European Journal of Human Genetics ·Harinder Gill, J.-M. Dorey, C. Mirella Spalluto, Angela Davies, K Muir, Danielle Velez, Bee Ling Ng, Nigel P. Carter, Caroline Mackie Ogilvie, David I. Wilson, Roland G. Roberts	2009	9
3	Comparative Genomic Hybridization: Microarray Design and Data Interpretation Methods in molecular biology ·Richard Redon, Nigel P. Carter	2009	12
4	Clinical implication of recurrent copy number alterations in hepatocellular carcinoma and putative oncogenes in recurrent gains on 1q International Journal of Cancer ·Tae‐Min Kim, Seon‐Hee Yim, Seung–Hun Shin, Максим Нестелєєв, Yuchae Jung, C. K. Park, Jong‐Young Choi, Won‐Sang Park, Miseon Kwon, Heike Fiegler, Nigel P. Carter, Mun‐Gan Rhyu, Yeun‐Jun Chung	2008	81
5	Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16 The American Journal of Human Genetics ·Irina Balikova, Kevin Martens, Cindy Melotte, Mustapha Amyere, Steven Van Vooren, Yves Moreau, David Vetrie, Heike Fiegler, Nigel P. Carter, Thomas Liehr, Miikka Vikkula, Gert Matthijs, Jean‐Pierre Fryns, Ingele Casteels, Koenraad Devriendt, Joris Vermeesch	2008	30
6	Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort The American Journal of Human Genetics ·Júlia Baptista, Catherine Mercer, Elena Prigmore, Susan Gribble, Nigel P. Carter, Viv Maloney, N. Simon Thomas, Patricia A. Jacobs, John A. Crolla	2008	127
7	Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12 European Journal of Medical Genetics ·Björn Menten, Karen Buysse, Stefan Vermeulen, Ramarolanto-Ratiaray, Jo Vandesompele, Bee Ling Ng, Nigel P. Carter, Geert Mortier, Frank Speleman	2007	11
8	Flow analysis and sorting of microchromosomes (<3 Mb) Cytometry Part A ·Bee Ling Ng, Fengtang Yang, Nigel P. Carter	2007	8
9	Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated with Autonomic Dysfunction The American Journal of Human Genetics ·Jeanne Amiel, Marlène Rio, Loïc de Pontual, Richard Redon, Valérie Malan, Nathalie Boddaert, Perrine Plouin, Nigel P. Carter, Stanislas Lyonnet, Arnold Münnich, Laurence Colleaux	2007	212
10	Germline rates of de novo meiotic deletions and duplications causing several genomic disorders Nature Genetics ·Daniel J. Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P. Carter, Martyn Blayney, Stephan Beck, Matthew E. Hurles	2007	225
11	Characterization of a 3;6 translocation associated with renal cell carcinoma Genes Chromosomes and Cancer ·Choi Chun Ho, Mahera Abdulrahman, Mark R. Morris, Elena Prigmore, Susan Gribble, Sukriadi, Dean Gentle, Steven Ready, Kanayo Umeh, Michael S. Wiesener, Takeshi Kishida, Masahiro Yao, Val Davison, José Luís Barbero, Carol Chu, Nigel P. Carter, Farida Latif, Eamonn R. Maher	2007	26
12	Challenges and standards in integrating surveys of structural variation Nature Genetics ·Stephen W. Scherer, Charles Lee, Ewan Birney, David Altshuler, Evan E. Eichler, Nigel P. Carter, Matthew E. Hurles, Lars Feuk	2007	280
13	Copy number variation: New insights in genome diversity Genome Research ·Jennifer L. Freeman, George H. Perry, Lars Feuk, Richard Redon, Steven A. McCarroll, David Altshuler, Hiroyuki Aburatani, Keith Jones, Chris Tyler‐Smith, Matthew E. Hurles, Nigel P. Carter, Stephen W. Scherer, Charles Lee Hit paper breakdown →	2006	592
14	Micro-array analyses decipher exceptional complex familial chromosomal rearrangement Human Genetics ·Christine Fauth, Susan Gribble, Keith Porter, M. Codina‐Pascual, Bee Ling Ng, Jürgen Kraus, Sabine Uhrig, Party Gurning, Thomas Haaf, Heike Fiegler, Nigel P. Carter, Michael R. Speicher	2006	17
15	Genome-Wide Screening of Genomic Alterations and Their Clinicopathologic Implications in Non–Small Cell Lung Cancers Clinical Cancer Research ·Tae‐Min Kim, Seon‐Hee Yim, Jung‐Sook Lee, Miseon Kwon, Zhen Enlong, Hyun Mi Kang, Heike Fiegler, Nigel P. Carter, Yeun‐Jun Chung	2005	59
16	Array Comparative Genomic Hybridization Analysis of Colorectal Cancer Cell Lines and Primary Carcinomas Cancer Research ·С.А. Исаев, Heike Fiegler, Andrew Rowan, Sarah Halford, David Bicknell, Walter F. Bodmer, Ian Tomlinson, Nigel P. Carter	2004	157
17	High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization Oncogene ·Carolyn D. Hurst, Heike Fiegler, Philippa Carr, Sarah Williams, Nigel P. Carter, Margaret A. Knowles	2004	121
18	A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome Human Genetics ·Katrina Prescott, Kathryn Woodfine, Laure Villemonté, Maurice Super, Bronwyn Kerr, Rodger Palmer, Nigel P. Carter, Peter Scambler	2004	22
19	Chromosome-specific paints from a high-resolution flow karyotype of the dog Chromosome Research ·Cordelia F. Langford, Patricia Fischer, M. M. Binns, Nigel G. Holmes, Nigel P. Carter	1996	76
20	Multiple self–healing squamous epitheliomata (ESS1) mapped to chromosome 9q22–q31 in families with common ancestry Nature Genetics ·David Goudie, Martin Yuille, Margaret Leversha, Robert A. Furlong, Nigel P. Carter, Michael Lush, Nabeel A. Affara, M.A. Ferguson‐Smith	1993	68

About Nigel P. Carter

Nigel P. Carter is a scholar working on Genetics, Plant Science, Pediatrics, Perinatology and Child Health, Molecular Biology and Cancer Research, having authored 98 papers that have together received 14.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (65 papers), Chromosomal and Genetic Variations (37 papers), Prenatal Screening and Diagnostics (19 papers), Gene expression and cancer classification (13 papers), Genomics and Chromatin Dynamics (12 papers), Congenital heart defects research (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (6.9k citations), Aging (339 citations), Molecular Biology (8.1k citations), Cancer Research (1.7k citations) and Plant Science (2.9k citations). Nigel P. Carter has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Heike Fiegler, Philippa Carr, Alan Tunnacliffe, Bruce A.J. Ponder, Matthew E. Hurles, Stephen P. Jackson, Fabrizio d’Adda di Fagagna, Gabriele Saretzki, Philip M. Reaper and Thomas von Zglinicki. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Genes Chromosomes and Cancer, Human Genetics and Chromosome Research.

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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