Peter M. Green

2.3k citations

19 papers · 928 indexed · h-index 15

Impact in

Hematology top 2%
- Hemophilia Treatment and Research
- Platelet Disorders and Treatments
- Blood Coagulation and Thrombosis Mechanisms
- Chronic Myeloid Leukemia Treatments
Immunology and Allergy top 10%
- Cell Adhesion Molecules Research

Papers in

Hematology 10
- Hemophilia Treatment and Research 8
- Blood Coagulation and Thrombosis Mechanisms 4
- Platelet Disorders and Treatments 3
Immunology and Allergy 2

Co-authors: F. Giannelli Richard D. Bagnall Naushin Waseem J.A. Naylor David Bentley Rachel Flomen Frances Flinter Rolf Ljung
Journals: Human Mutation (2 papers)The American Journal of Human Genetics (2 papers)Human Molecular Genetics (2 papers)Genes Chromosomes and Cancer (2 papers)Genomics (2 papers)
Partner nations: United Kingdom United States Qatar

In The Last Decade

Peter M. Green

19 papers receiving 898 citations

Peers

Countries citing papers authored by Peter M. Green

Since Specialization

Citations

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

Fields of papers citing papers by Peter M. Green

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 23 scholars most cited alongside Peter M. Green, 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 Peter M. Green Line = papers co-authored together Peter M. Green links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	A two-tier approach to mutation detection in theCOL4A5 gene for Alport syndrome Human Mutation ·Kathy King, Frances Flinter, Peter M. Green	2006	14
2	Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A Genome Research ·Richard D. Bagnall, Karen L. Ayres, Peter M. Green, F. Giannelli	2005	27
3	Mutation Detection in Factor VIII cDNA from Lymphocytes of Hemophilia A Patients by Solid Phase Fluorescent Chemical Cleavage of Mismatch Humana Press eBooks ·Naushin Waseem, Richard D. Bagnall, Peter M. Green, F. Giannelli	2003	1
4	Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A Blood ·Richard D. Bagnall, Naushin Waseem, Peter M. Green, F. Giannelli	2002	267
5	Biallelic Discrimination Assays for the Three Common Ashkenazi Jewish Mutations and a Common Non-Jewish Mutation, in Tay-Sachs Disease, Using Fluorogenic TaqMan Probes Genetic Testing ·T Gatti, Anthony H. Fensom, Peter M. Green	2000	6
6	The X Chromosome and the Rate of Deleterious Mutations in Humans The American Journal of Human Genetics ·F. Giannelli, Peter M. Green	2000	15
7	Detection of mutations in COL4A5 in patients with Alport Syndrome Human Mutation ·Kathryn E. Plant, Peter M. Green, David Vetrie, Frances Flinter	1999	49
8	DNA Variation in a 5-Mb Region of the X Chromosome and Estimates of Sex-Specific/Type-Specific Mutation Rates The American Journal of Human Genetics ·И А Царенко, Peter M. Green, G. Rowley, Cathryn M. Lewis, F. Giannelli	1999	25
9	Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patients British Journal of Haematology ·Richard D. Bagnall, Naushin Waseem, Peter M. Green, B T Colvin, Ilham Akbar Mulya Wibawa, F. Giannelli	1999	39
10	Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel‐Lindau tumor suppressor‐binding protein (CUL2 and VBP1) mutation and loss in renal‐cell carcinoma development Genes Chromosomes and Cancer ·Steven C. Clifford, 亜由美伊坂, Andréia Aparecida Guimarães Strohschoen, Elaine Green, Barnas Sabunga, Peter M. Green, Fahd Saud Attia Al-Thaqafi, Charis Eng, Eamonn R. Maher	1999	1
11	Genomic organization and chromosomal localization of the humanCUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma development Genes Chromosomes and Cancer ·Steven C. Clifford, 亜由美伊坂, Andréia Aparecida Guimarães Strohschoen, Elaine Green, Barnas Sabunga, Peter M. Green, Fahd Saud Attia Al-Thaqafi, Charis Eng, Eamonn R. Maher	1999	20
12	Characterization of the Gene (VBP1) and Transcript for the von Hippel–Lindau Binding Protein and Isolation of the Highly Conserved Murine Homologue Genomics ·Barnas Sabunga, Peter M. Green, F. Giannelli	1997	23
13	1 The molecular basis of haemophilia A and B Baillière s Clinical Haematology ·F. Giannelli, Peter M. Green	1996	34
14	Direct sequencing of PCR-amplified DNA Molecular Biotechnology ·Peter M. Green, F. Giannelli	1994	10
15	Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) gene Human Molecular Genetics ·Rachel Flomen, John Mukhopadhyay, Peter M. Green, David Bentley, F. Giannelli	1993	68
16	Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions Human Molecular Genetics ·J.A. Naylor, Barnas Sabunga, Raden Rifki, Peter M. Green, F. Giannelli	1993	189
17	Detection of point mutations and a gross deletion in six Hunter Syndrome patients Genomics ·Rachel Flomen, Peter M. Green, David Bentley, F. Giannelli, John Mukhopadhyay	1992	56
18	Haplotype Analysis of Identical Factor IX Mutants Using PCR Thrombosis and Haemostasis ·Peter M. Green, A.J. Montandon, Rolf Ljung, Galija Galiautdinova, F. Giannelli	1992	15
19	The incidence and distribution of CpG←Tpg transitions in the coagulation factor IX gene. A fresh look at CPG mutitional hospots Nucleic Acids Research ·Peter M. Green, Cindy Bitton, David Bentley, Rolf Ljung, Inga Marie Nilsson, F. Giannelli	1990	69

About Peter M. Green

Peter M. Green is a scholar working on Hematology, Immunology and Allergy, Physiology, Genetics and Molecular Biology, having authored 19 papers that have together received 928 indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (8 papers), Cancer-related gene regulation (8 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers), Platelet Disorders and Treatments (3 papers), Renal cell carcinoma treatment (2 papers), Epigenetics and DNA Methylation (2 papers), Connective tissue disorders research (2 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Hematology (541 citations), Immunology and Allergy (60 citations), Molecular Biology (606 citations), Genetics (82 citations) and Genetics (150 citations). Peter M. Green has collaborated with scholars based in United Kingdom, United States and Qatar. Frequent co-authors include F. Giannelli, Richard D. Bagnall, Naushin Waseem, J.A. Naylor, David Bentley, Rachel Flomen, Frances Flinter, Rolf Ljung, Kathryn E. Plant and Inga Marie Nilsson. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, Human Molecular Genetics, Genes Chromosomes and Cancer and Genomics.

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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