Adeline K. Nicholas

3.5k citations

26 papers · 2.1k indexed · 1 hit paper · h-index 15

Molecular Biology top 10%
Physiology top 5%
Cellular and Molecular Neuroscience top 5%
Genetics top 5%
Cell Biology top 5%

Co-authors: C. Geoffrey Woods James J. Cox Frank Reimann Emma Roberts Lihadh Al‐Gazali Fiona M. Gribble Gulshan Karbani Kelly Springell
Topics: Thyroid Disorders and Treatments (12 papers)Pain Mechanisms and Treatments (5 papers)Ion channel regulation and function (5 papers)
Cited by: Cellular and Molecular Neuroscience Sensory Systems Physiology
Journals: Nature Nature Genetics Journal of Neuroscience
Partner nations: United Kingdom Italy United States

In The Last Decade

Adeline K. Nicholas

24 papers receiving 2.0k 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 Adeline K. Nicholas

Since Specialization

Citations

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

Fields of papers citing papers by Adeline K. Nicholas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adeline K. Nicholas. 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 Adeline K. Nicholas. The network helps show where Adeline K. Nicholas may publish in the future.

Co-authorship network of co-authors of Adeline K. Nicholas

This figure shows the co-authorship network connecting the top 25 collaborators of Adeline K. Nicholas. A scholar is included among the top collaborators of Adeline K. Nicholas 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 Adeline K. Nicholas. Adeline K. Nicholas 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	Cervical cell lift: A novel triage method for the spatial mapping and grading of precancerous cervical lesions 2022 ·EBioMedicine ·(unknown),Nagayasu Egawa,Daniël M. Pelt,Robin Crawford,Adeline K. Nicholas,Veronika Romashova,Peter Sasieni,Heather Griffin,John Doorbar	6
2	Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism 2021 ·Thyroid ·(unknown),Adeline K. Nicholas,Erik Schoenmakers,Jennifer A. Dickens,Dhanapathi Halanaik,Jayaprakash Sahoo,Sadishkumar Kamalanathan,Nadia Schoenmakers	3
3	A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant 2021 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown),Nadia Schoenmakers,Adeline K. Nicholas,Eran Kassif,(unknown),Yonatan Yeshayahu	5
4	Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia 2020 ·Frontiers in Endocrinology ·(unknown),Mirjana Kočova,Adeline K. Nicholas,(unknown),Nadia Schoenmakers	12
5	DUOX2 / DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom 2019 ·Thyroid ·Catherine Peters,Adeline K. Nicholas,Erik Schoenmakers,Greta Lyons,(unknown),Eva Serra,Neil J. Sebire,Marina Muzza,Laura Fugazzola,Nadia Schoenmakers	33
6	Haploinsufficiency of <b><i>NKX2-1</i></b> in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction 2019 ·Hormone Research in Paediatrics ·Rathi Prasad,Adeline K. Nicholas,Nadia Schoenmakers,John Barton	10
7	A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome 2018 ·Clinical Endocrinology ·Edna Roche,Anne McGowan,Olympia Koulouri,Marc‐Olivier Turgeon,Adeline K. Nicholas,(unknown),Ranna El‐Khairi,Noina Abid,Greta Lyons,David Halsall,Marco Bonomi,Luca Persani,Mehul Dattani,Mark Gurnell,Daniel J. Bernard,Nadia Schoenmakers	17
8	A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism 2016 ·The Journal of Clinical Endocrinology & Metabolism ·Olympia Koulouri,Adeline K. Nicholas,Erik Schoenmakers,Jacek Mokrosiński,(unknown),Tim Cole,Jeremy Kirk,I. Sadaf Farooqi,Krishna Chatterjee,Mark Gurnell,Nadia Schoenmakers	17
9	Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency 2016 ·Journal of Allergy and Clinical Immunology ·Chiara Bacchelli,Federico A. Moretti,Marlene Carmo,Stuart Adams,Horia Stanescu,Kerra Pearce,Manisha Madkaikar,Kimberly Gilmour,Adeline K. Nicholas,C. Geoffrey Woods,Robert Kleta,Phil Beales,Waseem Qasim,H. Bobby Gaspar	31
10	NovelSCN9AMutations Underlying Extreme Pain Phenotypes: Unexpected Electrophysiological and Clinical Phenotype Correlations 2015 ·Journal of Neuroscience ·Edward C. Emery,Abdella M. Habib,James J. Cox,Adeline K. Nicholas,Fiona M. Gribble,C. Geoffrey Woods,Frank Reimann	41
11	A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism 2013 ·Nadia Schoenmakers,Hakan Cangül,Adeline K. Nicholas,Erik Schoenmakers,Greta Lyons,Mehul Dattani,Catherine Peters,(unknown),Abdelhadi Habeb,Asma Deeb,(unknown),Soo‐Mi Park,Marina Muzza,Luca Persani,Laura Fugazzola,Eamonn R. Maher,(unknown)	8
12	A primary microcephaly protein complex forms a ring around parental centrioles 2011 ·Nature Genetics ·(unknown),Alexis R. Barr,Adeline K. Nicholas,Ofélia P. Carvalho,(unknown),(unknown),Stefanie Reichelt,Clive S. D’Santos,C. Geoffrey Woods,Fanni Gergely	172
13	A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy 2010 ·Journal of Medical Genetics ·Ofélia P. Carvalho,(unknown),Jozef Hertecant,Henry Houlden,Adeline K. Nicholas,James J. Cox,(unknown),Lihadh Al‐Gazali,C. Geoffrey Woods	66
14	Age-related gene-specific changes of A-to-I mRNA editing in the human brain 2010 ·Mechanisms of Ageing and Development ·Adeline K. Nicholas,João Pedro de Magalhães,Yevgenya Kraytsberg,Eric K. Richfield,Erez Y. Levanon,Konstantin Khrapko	41
15	Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations 2010 ·Human Mutation ·James J. Cox,Jony Sheynin,Zamir Shorer,Frank Reimann,Adeline K. Nicholas,(unknown),Marco Baralle,Elizabeth Wraige,Esther Manor,Jacov Levy,Crislyn Woods,Ruti Parvari	84
16	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
17	Two novel SCN9A mutations causing insensitivity to pain 2009 ·Pain ·Kristian Bernhard Nilsen,Adeline K. Nicholas,C. Geoffrey Woods,Svein Ivar Mellgren,(unknown),Jan Aasly	78
18	Absence of pain with hyperhidrosis: A new syndrome where vascular afferents may mediate cutaneous sensation 2009 ·Pain ·David Bowsher,Geoffrey Woods,Adeline K. Nicholas,(unknown),(unknown),(unknown),J. M. MacKenzie,Daniel Crooks,(unknown),(unknown),(unknown),(unknown),James Wymer,Phillip J. Albrecht,Charles E. Argoff,Frank L. Rice	25
19	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
20	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

About Adeline K. Nicholas

Adeline K. Nicholas is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Physiology, having authored 26 papers that have together received 2.1k indexed citations. Recurring topics across this work include Thyroid Disorders and Treatments (12 papers), Pain Mechanisms and Treatments (5 papers) and Ion channel regulation and function (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (569 citations), Sensory Systems (146 citations) and Physiology (754 citations). Adeline K. Nicholas has collaborated with scholars based in United Kingdom, Italy and United States. Frequent co-authors include C. Geoffrey Woods, James J. Cox, Frank Reimann, Emma Roberts, Lihadh Al‐Gazali, Fiona M. Gribble, Gulshan Karbani, Kelly Springell, John N. Wood and Hussain Jafri. Their work appears in journals such as Nature, Nature Genetics and Journal of Neuroscience.

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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