Emma Roberts

5.5k citations

21 papers · 3.4k indexed · 1 hit paper · h-index 18

Molecular Biology top 5%
Genetics top 2%
Cell Biology top 1%
Physiology top 5%
Cellular and Molecular Neuroscience top 5%

Co-authors: C. Geoffrey Woods Kelly Springell Hussain Jafri Gulshan Karbani Daniel J. Hampshire Jacquelyn Bond James J. Cox Yasmin Abdul Rashid
Topics: Microtubule and mitosis dynamics (8 papers)Genetics and Neurodevelopmental Disorders (4 papers)Mitochondrial Function and Pathology (3 papers)
Cited by: Cell Biology Developmental Neuroscience Genetics
Journals: Nature Nucleic Acids Research Nature Genetics
Partner nations: United Kingdom United States Pakistan

In The Last Decade

Emma Roberts

21 papers receiving 3.3k 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.

An SCN9A channelopathy causes congenital inability to experience pain

2006 1.1k citations James J. Cox, Frank Reimann et al. Nature profile →

Peers

Countries citing papers authored by Emma Roberts

Since Specialization

Citations

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

Fields of papers citing papers by Emma Roberts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Roberts

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Roberts. A scholar is included among the top collaborators of Emma Roberts 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 Roberts. Emma Roberts 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	Skin Cancer Risk Is Increased by Somatic Mutations Detected Noninvasively in Healthy-Appearing Sun-Exposed Skin 2024 ·Journal of Investigative Dermatology ·(unknown),Rizi Ai,(unknown),(unknown),Emma Roberts,Erica N. Montano,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),John Dobak,(unknown),Burkhard Jansen,Loren E. Clarke,Steven Stone,John W. Whitaker	1
2	Are we good and are we safe? Measuring quality and assessing risk in an adult autism diagnostic service 2017 ·Advances in Autism ·(unknown),(unknown),(unknown),(unknown),Emma Roberts,Bhavika Patel,(unknown)	1
3	Human ASPM participates in spindle organisation, spindle orientation and cytokinesis 2010 ·BMC Cell Biology ·J. William Higgins,Carol Midgley,(unknown),Sandra Bell,(unknown),Emma Roberts,(unknown),Saghira Malik Sharif,Christopher Bennett,David M. Glover,C. Geoffrey Woods,Ewan E. Morrison,Jacquelyn Bond	95
4	WDR62 is associated with the spindle pole and is mutated in human microcephaly 2010 ·Nature Genetics ·Adeline K. Nicholas,(unknown),Julie Désir,Ofélia P. Carvalho,James J. Cox,(unknown),Rizwana Kausar,Muhammad Ansar,Wasim Ahmad,Alain Verloès,Sandrine Passemard,(unknown),Susan Lindsay,Fanni Gergely,William B. Dobyns,Emma Roberts,Marc Abramowicz,C. Geoffrey Woods	211
5	An SCN9A channelopathy causes congenital inability to experience painbreakdown → 2006 ·Nature ·James J. Cox,Frank Reimann,Adeline K. Nicholas,(unknown),Emma Roberts,Kelly Springell,Gulshan Karbani,Hussain Jafri,(unknown),Yasmin Raashid,Lihadh Al‐Gazali,(unknown),Enza Maria Valente,Shaun Gorman,Richard Williams,Duncan P. McHale,John N. Wood,Fiona M. Gribble,C. Geoffrey Woods	1094
6	Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome 2006 ·The American Journal of Human Genetics ·C. Geoffrey Woods,Sigmar Stricker,Petra Seemann,Rowena Stern,James J. Cox,(unknown),Emma Roberts,Kelly Springell,Simon Scott,Gulshan Karbani,Saghira Malik Sharif,Carmel Toomes,Jacquelyn Bond,Dheeraj Kumar,Lihadh Al‐Gazali,Stefan Mundlos	116
7	MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34 2006 ·European Journal of Human Genetics ·Daniel J. Hampshire,Muhammad Ayub,Kelly Springell,Emma Roberts,Hussain Jafri,Yasmin Abdul Rashid,Jacquelyn Bond,John Riley,C. Geoffrey Woods	52
8	A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size 2005 ·Nature Genetics ·Jacquelyn Bond,Emma Roberts,Kelly Springell,(unknown),(unknown),J. William Higgins,Daniel J. Hampshire,Ewan E. Morrison,(unknown),Elias O. Silva,(unknown),Diana Baralle,Michela Raponi,Gulshan Karbani,Yasmin Abdul Rashid,Hussain Jafri,Christopher Bennett,Peter Corry,Christopher A. Walsh,C. Geoffrey Woods	423
9	Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size 2003 ·The American Journal of Human Genetics ·Jacquelyn Bond,(unknown),Daniel J. Hampshire,Kelly Springell,Peter Corry,Marc Abramowicz,Ganeshwaran H. Mochida,Raoul C. M. Hennekam,Eamonn R. Maher,Jean‐Pierre Fryns,Abdulrahman Alswaid,Hussain Jafri,Yasmin Abdul Rashid,Ammar F. Mubaidin,Christopher A. Walsh,Emma Roberts,C. Geoffrey Woods	133
10	ASPM is a major determinant of cerebral cortical size 2002 ·Nature Genetics ·Jacquelyn Bond,Emma Roberts,Ganeshwaran H. Mochida,Daniel J. Hampshire,(unknown),(unknown),Kelly Springell,Meera Mahadevan,Yanick J. Crow,Alexander F. Markham,Christopher A. Walsh,C. Geoffrey Woods	420
11	Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation 2002 ·Journal of Medical Genetics ·Emma Roberts,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	94
12	Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain 2002 ·The American Journal of Human Genetics ·Andrew P. Jackson,(unknown),Sandra Bell,Jimi Adu,Carmel Toomes,Ian Carr,Emma Roberts,Daniel J. Hampshire,Yanick J. Crow,Alan J. Mighell,Gulshan Karbani,Hussain Jafri,Yasmin Abdul Rashid,Robert F. Mueller,Alexander F. Markham,C. Geoffrey Woods	340
13	A New Locus for Autosomal Dominant Familial Exudative Vitreoretinopathy Maps to Chromosome 11p12-13 2001 ·The American Journal of Human Genetics ·Louise Downey,T J Keen,Emma Roberts,David Mansfield,Mahfouth A. Bamashmus,Chris F. Inglehearn	49
14	A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34 2000 ·The American Journal of Human Genetics ·Leanne Moynihan,Andrew P. Jackson,Emma Roberts,Gulshan Karbani,Ian Lewis,Peter Corry,G Turner,Robert F. Mueller,Nicholas Lench,C. Geoffrey Woods	81
15	A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23–q31 2000 ·European Journal of Human Genetics ·(unknown),Andrew P. Jackson,Emma Roberts,(unknown),(unknown),Mark Houseman,(unknown),Nicholas Lench,(unknown),(unknown)	19
16	A Fifth Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 1q31 2000 ·The American Journal of Human Genetics ·(unknown),Yanick J. Crow,(unknown),Andrew P. Jackson,Hussain Jafri,Yasmin Abdul Rashid,Emma Roberts,C. Geoffrey Woods	72
17	The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1–13.2 1999 ·European Journal of Human Genetics ·Emma Roberts,Andrew P. Jackson,(unknown),(unknown),(unknown),Yasmin Abdul Rashid,Hussain Jafri,Duncan P. McHale,Alex Markham,Nicholas Lench,C. Geoffrey Woods	79
18	Comparison of Enzyme Mismatch Cleavage and Chemical Cleavage of Mismatch on a Defined Set of Heteroduplexes 1997 ·Genetic Testing ·(unknown),Emma Roberts,Mark D. Robinson,C. Geoffrey Woods,D. Timothy Bishop,Graham R. Taylor	7
19	Potassium permanganate and tetraethylammonium chloride are a safe and effective substitute for osmium tetroxide in solid-phase fluorescent chemical cleavage of mismatch 1997 ·Nucleic Acids Research ·Emma Roberts	38
20	Ectopic expression of inactive forms of yeast DNA topoisomerase II confers resistance to the anti-tumour drug, etoposide 1996 ·British Journal of Cancer ·(unknown),(unknown),Emma Roberts,Susan M. Gasser	25

About Emma Roberts

Emma Roberts is a scholar working on Cell Biology, Developmental Biology and Sensory Systems, having authored 21 papers that have together received 3.4k indexed citations. Recurring topics across this work include Microtubule and mitosis dynamics (8 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Cell Biology (1.0k citations), Developmental Neuroscience (234 citations) and Genetics (1.1k citations). Emma Roberts has collaborated with scholars based in United Kingdom, United States and Pakistan. Frequent co-authors include C. Geoffrey Woods, Kelly Springell, Hussain Jafri, Gulshan Karbani, Daniel J. Hampshire, Jacquelyn Bond, James J. Cox, Yasmin Abdul Rashid, Adeline K. Nicholas and Lihadh Al‐Gazali. Their work appears in journals such as Nature, Nucleic Acids Research and Nature 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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