Emma Kivuva

2.8k total citations
12 papers, 369 citations indexed

About

Emma Kivuva is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Emma Kivuva has authored 12 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Emma Kivuva's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Emma Kivuva is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Emma Kivuva collaborates with scholars based in United Kingdom, United States and France. Emma Kivuva's co-authors include Sahar Mansour, Sunayna Best, Jane Hayward, Alison Male, Lyn S. Chitty, Natalie Chandler, Francesca Faravelli, Dagmar Tapon, Catherine DeVile and Peter D. Turnpenny and has published in prestigious journals such as Nature Communications, Journal of Medical Genetics and Clinical Endocrinology.

In The Last Decade

Emma Kivuva

12 papers receiving 354 citations

Peers

Countries citing papers authored by Emma Kivuva

Since Specialization

Citations

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

Fields of papers citing papers by Emma Kivuva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Kivuva

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Kivuva. A scholar is included among the top collaborators of Emma Kivuva 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 Emma Kivuva. Emma Kivuva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development 2024 ·Nature Communications ·Fabiola Ceroni, (unknown), Richard Holt, Елена А. Сорокина, Nicolas Chassaing, Samuel Clokie, Thomas Naert, (unknown), Sanaa Muheisen, Dorine A. Bax, Yeşim Kesim, Emma Kivuva, (unknown), Soeren S. Lienkamp, Julie Plaisancié, Elfride De Baere, Patrick Calvas, Kris Vleminckx, Elena V. Semina, Nicola Ragge	2
2	Systematic assessment of outcomes following a genetic diagnosis identified through a large-scale research study into developmental disorders 2021 ·Genetics in Medicine ·Hannah Copeland, Emma Kivuva, Helen V. Firth, Caroline F. Wright	8
3	Rapid Prenatal Diagnosis Using Targeted Exome Sequencing: A Cohort Study to Assess Feasibility and Potential Impact on Prenatal Counseling and Pregnancy Management 2019 ·Obstetrical & Gynecological Survey ·Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S. Chitty	2
4	Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management 2018 ·Genetics in Medicine ·Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S. Chitty	104
5	Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA 2015 ·Journal of Molecular Medicine ·Margriet van Kogelenberg, Alice R. Clark, Zandra A. Jenkins, Tim Morgan, (unknown), Gregory M. Sawyer, Matthew Edwards, Tracy Dudding, Tessa Homfray, Bruce Castle, John Tolmie, Fiona Stewart, Emma Kivuva, Daniela T. Pilz, Michael T. Gabbett, Andrew J. Sutherland‐Smith, Stephen P. Robertson	9
6	SOS1 frameshift mutations cause pure mucosal neuroma syndrome, a clinical phenotype distinct from multiple endocrine neoplasia type 2B 2015 ·Clinical Endocrinology ·Martina Owens, Emma Kivuva, Anthony Quinn, Paul Brennan, Richard Caswell, Hana Lango Allen, Bijay Vaidya, Sian Ellard	10
7	An exome sequencing strategy to diagnose lethal autosomal recessive disorders 2014 ·European Journal of Human Genetics ·Sian Ellard, Emma Kivuva, Peter D. Turnpenny, Karen Stals, Matthew B. Johnson, Weijia Xie, Richard Caswell, Hana Lango Allen	36
8	Inherited dup(17)(p11.2p11.2): Expanding the phenotype of the Potocki–Lupski syndrome 2013 ·American Journal of Medical Genetics Part A ·Pilar Magoulas, Pengfei Liu, Violet Gelowani, Claudia Soler‐Alfonso, Emma Kivuva, James R. Lupski, Lorraine Potocki	23
9	Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay 2011 ·American Journal of Medical Genetics Part A ·Eric Muller, Swaroop Aradhya, Joan Atkin, Erin P. Carmany, Alison M. Elliott, Albert E. Chudley, Robin D. Clark, David B. Everman, (unknown), Bryan D. Hall, Gail E. Herman, Emma Kivuva, (unknown), David A. Stevenson, David W. Stockton, Louanne Hudgins	42
10	CHRNG genotype–phenotype correlations in the multiple pterygium syndromes 2011 ·Journal of Medical Genetics ·Julie Vogt, Neil V. Morgan, (unknown), Laurence Bonhomme‐Faivre, Louise Brueton, Kristin Becker, Jean‐Pierre Fryns, Sue Holder, Lily Islam, Emma Kivuva, Sally Ann Lynch, Renaud Touraine, Louise C. Wilson, Fiona MacDonald, Eamonn R. Maher	30
11	Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci 2010 ·European Journal of Human Genetics ·Claire Turner, Deborah Mackay, Jonathan L A Callaway, Louise E Docherty, Rebecca Poole, H. Bullman, Margaret Lever, Bruce Castle, Emma Kivuva, Peter D. Turnpenny, Sarju Mehta, Sahar Mansour, Emma Wakeling, Verghese Mathew, J. Madden, Justin H. Davies, I. Karen Temple	73
12	De Barsy syndrome: a review of the phenotype 2008 ·Clinical Dysmorphology ·Emma Kivuva, Michael Parker, Marta C. Cohen, Bart Wagner, Glenda Sobey	30

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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