Mary Petrou

2.5k citations

63 papers · 1.7k indexed · h-index 25

Impact in

Genetics top 0.5%
- Hemoglobinopathies and Related Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Hematology top 1%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in

Genetics 45
- Hemoglobinopathies and Related Disorders 45
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
Hematology 21
- Iron Metabolism and Disorders 16
- Blood groups and transfusion 5

Co-authors: B. Modell Bernadette Modell Suhaib Ahmed R. H. T. Ward Julie M. Old Jon Sherlock Matteo Adinolfí Vincenzo Cirigliano
Journals: Prenatal Diagnosis (8 papers)British Journal of Haematology (4 papers)Journal of Medical Genetics (4 papers)The Lancet (4 papers)Annals of the New York Academy of Sciences (3 papers)
Partner nations: United Kingdom Italy Pakistan

In The Last Decade

Mary Petrou

63 papers receiving 1.6k citations

Peers

Countries citing papers authored by Mary Petrou

Since Specialization

Citations

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

Fields of papers citing papers by Mary Petrou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary Petrou. 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 Mary Petrou. The network helps show where Mary Petrou may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Mary Petrou, 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 Mary Petrou Line = papers co-authored together Mary Petrou links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The parental perspective of thalassaemia in Bangladesh: lack of knowledge, regret, and barriers Orphanet Journal of Rare Diseases ·Mohammad Sorowar Hossain, Md. Mahbub Hasan, Mary Petrou, Paul Telfer, Abdullah Al Mosabbir	2021	11
2	Thalassaemia control in developing counties- the Sri Lankan perspective Ceylon Medical Journal ·Laura Dovero, Ashwin Anenden, Junyue Yin, Mary Petrou	2015	1
3	EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies European Journal of Human Genetics ·(unknown), Joanne Traeger‐Synodinos, Cornelis L. Harteveld, John Old, Mary Petrou, Renzo Galanello, Piero C. Giordano, Yanlin Nie, Barbara De la Salle, Shirley Henderson, Alison May	2014	74
4	Screening for beta thalassaemia Indian journal of human genetics ·Mary Petrou	2010	16
5	Preimplantation Genetic Diagnosis Hemoglobin ·Mary Petrou	2009	6
6	A Different Molecular Pattern of β‐Thalassemia Mutations in Northeast Brazil Hemoglobin ·Aderson S. Araújo, Wilson A. Silva, Y Catonné, GN Bowden, Mary Petrou, Bernadette Modell, Marco A. Zago	2003	22
7	Sperm DNA damage in potentially fertile homozygous -thalassaemia patients with iron overload Human Reproduction ·احسان فکور, Arnold Pizzey, 道彦北村, M Katz, John B. Porter, Mary Petrou, D. Stewart Irvine, R Chatterjee	2002	46
8	Screening Extended Families for Genetic Hemoglobin Disorders in Pakistan New England Journal of Medicine ·Suhaib Ahmed, Кинцанс Владимир, Bernadette Modell, Mary Petrou	2002	136
9	Long-term effect of prospective detection of high genetic risk on couples' reproductive life: data for thalassaemia Prenatal Diagnosis ·Mary Petrou, Bernadette Modell, Л. В. Горбуненко, Violeta Balinskaite, R. H. T. Ward	2000	16
10	THE LABORATORY DIAGNOSIS OF HAEMOGLOBINOPATHIES British Journal of Haematology ·Barbara J. Bain, R. Amos, D. Bareford, 健二川村, Sally C. Davies, Julie M. Old, Barbara Wild, I. Cavill, Keith Hyde, E Matutes, John F. Reilly, Mary Petrou, D. Mark Layton, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1998	102
11	Assessment of quantitative fluorescent multiplex PCR performed on single cells UCL Discovery (University College London) ·Jon Sherlock, Vincenzo Cirigliano, Mary Petrou, B. Tutschek, Matteo Adinolfí	1998	2
12	Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells Annals of Human Genetics ·Jon Sherlock, Vincenzo Cirigliano, Mary Petrou, B. Tutschek, Matteo Adinolfí	1998	73
13	Detection of haemoglobinopathies and chromosome aneuploidy from minute DNA samples using multiplex PCR UCL Discovery (University College London) ·Jon Sherlock, Vincenzo Cirigliano, Mary Petrou, Daniel Wells, Matteo Adinolfí	1997	1
14	Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 years BMJ ·B. Modell, Mary Petrou, Mark Layton, Christine Slater, Leslie Müller Pinochet, CH Rodeck, J. Riedlinger, K. H. Nicolaides, Simon Gibbons, Alison Fitches, Julie M. Old	1997	53
15	PRENATAL DETECTION OF Hb MUTATIONS USING TRANSCERVICAL CELLS Prenatal Diagnosis ·Matteo Adinolfí, 窪田泰夫, Jon Sherlock, R. H. T. Ward, Mary Petrou, CH Rodeck	1997	16
16	Identification of novel Asian Indian and Japanese mutations causing β-thalassaemia in the Egyptian population Human Genetics ·窪田泰夫, Mary Petrou, Juan José E. Changllio-Roas, Katrin P. Hagen, Stephen Simon Gideon, Joy Delhanty	1997	26
17	Hereditary anaemias and iron deficiency in a tribal population (the Baiga) of central India European Journal Of Haematology ·P. H. Reddy, Mary Petrou, (unknown), (unknown), Ciaran Kohli‐Lynch, B. Modell	1995	19
18	Alpha thalassaemia hydrops fetalis in the UK: the importance of screening pregnant women of Chinese, other South East Asian and Mediterranean extraction for alpha thalassaemia trait BJOG An International Journal of Obstetrics & Gynaecology ·Mary Petrou, Maura Brugiatelli, Julie M. Old, T. Lettinga, R. H. T. Ward, Peter Wildeblood, CH Rodeck, B. Modell	1992	20
19	Changes in circulating alphafetoprotein and human chorionic gonadotrophin following chorionic villus sampling European Journal of Obstetrics & Gynecology and Reproductive Biology ·P. Daniel Knott, Brian Chan, R. H. T. Ward, T. Chard, J. G. Grudzinskas, Mary Petrou, B. Modell	1988	8
20	Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound. BMJ ·R. H. T. Ward, B. Modell, Mary Petrou, 庄司学, 周智松	1983	107

About Mary Petrou

Mary Petrou is a scholar working on Genetics, Hematology, Pediatrics, Perinatology and Child Health, Obstetrics and Gynecology and Genetics, having authored 63 papers that have together received 1.7k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (45 papers), Prenatal Screening and Diagnostics (24 papers), Iron Metabolism and Disorders (16 papers), Pregnancy and preeclampsia studies (5 papers), Blood groups and transfusion (5 papers), Parvovirus B19 Infection Studies (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (1.1k citations), Hematology (802 citations), Pediatrics, Perinatology and Child Health (728 citations), Genetics (269 citations) and Infectious Diseases (117 citations). Mary Petrou has collaborated with scholars based in United Kingdom, Italy and Pakistan. Frequent co-authors include B. Modell, Bernadette Modell, Suhaib Ahmed, R. H. T. Ward, Julie M. Old, Jon Sherlock, Matteo Adinolfí, Vincenzo Cirigliano, John Old and Mohammad Saleem. Their work appears in journals such as Prenatal Diagnosis, British Journal of Haematology, Journal of Medical Genetics, The Lancet and Annals of the New York Academy of Sciences.

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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