Kelly Springell

4.2k citations

13 papers · 2.7k indexed · 1 hit paper · h-index 11

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

Co-authors: C. Geoffrey Woods Emma Roberts Gulshan Karbani Jacquelyn Bond Hussain Jafri Daniel J. Hampshire James J. Cox Lihadh Al‐Gazali
Topics: Genetics and Neurodevelopmental Disorders (6 papers)Microtubule and mitosis dynamics (4 papers)Retinal Development and Disorders (2 papers)
Cited by: Cell Biology Developmental Neuroscience Genetics
Journals: Nature Nature Genetics Brain
Partner nations: United Kingdom United States India

In The Last Decade

Kelly Springell

13 papers receiving 2.6k 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 Kelly Springell

Since Specialization

Citations

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

Fields of papers citing papers by Kelly Springell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelly Springell

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes 2010 ·Human Mutation ·Katherine V. Towns,(unknown),Vernon Long,Martin McKibbin,C. Maubaret,Veronika Vaclavik,Parastoo Ehsani,Kelly Springell,Mohammed Kamal,Raj Ramesar,David A. Mackey,Anthony T. Moore,(unknown),Andrew R. Webster,Graeme C. Black,James O’Sullivan,Shomi S. Bhattacharya,Eric A. Pierce,Jean D. Beggs,Chris F. Inglehearn	30
2	Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia 2009 ·The American Journal of Human Genetics ·Mohammad Reza Abdollahi,Ewan E. Morrison,Tamara Sirey,Zoltán Molnár,Bruce E. Hayward,Ian Carr,Kelly Springell,(unknown),Mushtaq Ahmed,(unknown),Peter Corry,Daniela T. Pilz,Neil Stoodley,Yanick J. Crow,Graham R. Taylor,David T. Bonthron,Eamonn Sheridan	122
3	MACULAR DYSTROPHY ASSOCIATED WITH THE ARG172TRP SUBSTITUTION IN PERIPHERIN/RDS 2009 ·Retina ·Seema Anand,Eamonn Sheridan,(unknown),Chris F. Inglehearn,G. A. Williams,Kelly Springell,Victoria Allgar,Thu‐Lan Kelly,Martin McKibbin	4
4	The molecular landscape of ASPM mutations in primary microcephaly 2008 ·Journal of Medical Genetics ·Adeline K. Nicholas,Eric A. Swanson,James J. Cox,Gulshan Karbani,(unknown),Kelly Springell,Daniel J. Hampshire,M Ahmed,Jacquelyn Bond,Daniela Benedetto,Marco Fichera,Corrado Romano,William B. Dobyns,C. Geoffrey Woods	68
5	Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect 2006 ·European Journal of Human Genetics ·Mireille Cossée,Bénédicte Demeer,Patricia Blanchet,Bernard Échenne,Deepika Singh,(unknown),(unknown),(unknown),Louis Vallée,Hélène Dollfus,Sridevi Hegde,Kelly Springell,B.K. Thelma,Geoffrey Woods,Vera M. Kalscheuer,Jean‐Louis Mandel	19
6	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
7	Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease 2006 ·The American Journal of Human Genetics ·C. Geoffrey Woods,James J. Cox,Kelly Springell,Daniel J. Hampshire,Moin Mohamed,Martin McKibbin,Rowena Stern,F. Lucy Raymond,Richard Sandford,Saghira Malik Sharif,Gulshan Karbani,(unknown),Jacquelyn Bond,David Clayton,Chris F. Inglehearn	192
8	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
9	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
10	Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16 2005 ·Brain ·Kate Chandler,(unknown),Karl Rakshi,Kelly Springell,(unknown),Neil Stoodley,C. Geoffrey Woods,Daniela T. Pilz	6
11	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
12	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
13	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

About Kelly Springell

Kelly Springell is a scholar working on Developmental Biology, Cell Biology and Genetics, having authored 13 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Microtubule and mitosis dynamics (4 papers) and Retinal Development and Disorders (2 papers). The work is most often cited by research in Cell Biology (664 citations), Developmental Neuroscience (167 citations) and Genetics (823 citations). Kelly Springell has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include C. Geoffrey Woods, Emma Roberts, Gulshan Karbani, Jacquelyn Bond, Hussain Jafri, Daniel J. Hampshire, James J. Cox, Lihadh Al‐Gazali, Christopher A. Walsh and Adeline K. Nicholas. Their work appears in journals such as Nature, Nature Genetics and Brain.

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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