Adeline K. Nicholas

3.5k citations

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

Cellular and Molecular Neuroscience top 5%
Sensory Systems top 2%
Physiology top 5%
- Pain Mechanisms and Treatments 5
Cell Biology top 5%
- Microtubule and mitosis dynamics 3
Molecular Biology top 10%
- Ion channel regulation and function 5
- Congenital heart defects research 4
Endocrinology, Diabetes and Metabolism
- Thyroid Disorders and Treatments 12
- Growth Hormone and Insulin-like Growth Factors 3
Genetics
- Genetic Syndromes and Imprinting 3
Pulmonary and Respiratory Medicine
- Neonatal Respiratory Health Research 3

Co-authors: C. Geoffrey Woods James J. Cox Frank Reimann Emma Roberts Lihadh Al‐Gazali Fiona M. Gribble Gulshan Karbani Kelly Springell
Cited by: Cellular and Molecular Neuroscience Sensory Systems Physiology
Journals: Nature Genetics (2 papers)Journal of Medical Genetics (2 papers)Pain (2 papers)
Partner nations: United Kingdom Italy United States

In The Last Decade

Adeline K. Nicholas

24 papers receiving 2.0k citations

Hit Papers

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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

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

All Works

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20 of 20 papers shown

#	Work
1	Cervical cell lift: A novel triage method for the spatial mapping and grading of precancerous cervical lesions EBioMedicine ·M. K. Williams,Nagayasu Egawa,Daniël M. Pelt,Robin Crawford,Adeline K. Nicholas,Veronika Romashova,Peter Sasieni,Heather Griffin,John Doorbar	2022	6
2	Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism Thyroid ·Xiusha Wei,Adeline K. Nicholas,Erik Schoenmakers,Jennifer A. Dickens,Dhanapathi Halanaik,Jayaprakash Sahoo,Sadishkumar Kamalanathan,Nadia Schoenmakers	2021	3
3	A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant Journal of Clinical Research in Pediatric Endocrinology ·Andrea Derix,Nadia Schoenmakers,Adeline K. Nicholas,Eran Kassif,Eko Agus Purwanto,Yonatan Yeshayahu	2021	5
4	Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia Frontiers in Endocrinology ·稔齋藤,Mirjana Kočova,Adeline K. Nicholas,Tony Germans,Nadia Schoenmakers	2020	12
5	DUOX2 / DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom Thyroid ·Catherine Peters,Adeline K. Nicholas,Erik Schoenmakers,Greta Lyons,Jyoti Rasogi,Eva Serra,Neil J. Sebire,Marina Muzza,Laura Fugazzola,Nadia Schoenmakers	2019	33
6	Haploinsufficiency of <b><i>NKX2-1</i></b> in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction Hormone Research in Paediatrics ·Rathi Prasad,Adeline K. Nicholas,Nadia Schoenmakers,John Barton	2019	10
7	A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome Clinical Endocrinology ·Edna Roche,Anne McGowan,Olympia Koulouri,Marc‐Olivier Turgeon,Adeline K. Nicholas,C.W.C. Dunnington,Ranna El‐Khairi,Noina Abid,Greta Lyons,David Halsall,Marco Bonomi,Luca Persani,Mehul Dattani,Mark Gurnell,Daniel J. Bernard,Nadia Schoenmakers	2018	17
8	A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism The Journal of Clinical Endocrinology & Metabolism ·Olympia Koulouri,Adeline K. Nicholas,Erik Schoenmakers,Jacek Mokrosiński,光朝大根,Tim Cole,Jeremy Kirk,I. Sadaf Farooqi,Krishna Chatterjee,Mark Gurnell,Nadia Schoenmakers	2016	17
9	Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency 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	2016	31
10	NovelSCN9AMutations Underlying Extreme Pain Phenotypes: Unexpected Electrophysiological and Clinical Phenotype Correlations Journal of Neuroscience ·Edward C. Emery,Abdella M. Habib,James J. Cox,Adeline K. Nicholas,Fiona M. Gribble,C. Geoffrey Woods,Frank Reimann	2015	41
11	A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism Nadia Schoenmakers,Hakan Cangül,Adeline K. Nicholas,Erik Schoenmakers,Greta Lyons,Mehul Dattani,Catherine Peters,Jyoti Rasogi,Abdelhadi Habeb,Asma Deeb,F. Zhang,Soo‐Mi Park,Marina Muzza,Luca Persani,Laura Fugazzola,Eamonn R. Maher,Akio SHINOZAKI	2013	8
12	A primary microcephaly protein complex forms a ring around parental centrioles Nature Genetics ·旦永井,Alexis R. Barr,Adeline K. Nicholas,Ofélia P. Carvalho,李志欣,Zeng He-lan,Stefanie Reichelt,Clive S. D’Santos,C. Geoffrey Woods,Fanni Gergely	2011	172
13	A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy Journal of Medical Genetics ·Ofélia P. Carvalho,Saigusa Shigeru,Jozef Hertecant,Henry Houlden,Adeline K. Nicholas,James J. Cox,Nikolaos Zisis,Lihadh Al‐Gazali,C. Geoffrey Woods	2010	66
14	Age-related gene-specific changes of A-to-I mRNA editing in the human brain Mechanisms of Ageing and Development ·Adeline K. Nicholas,João Pedro de Magalhães,Yevgenya Kraytsberg,Eric K. Richfield,Erez Y. Levanon,Konstantin Khrapko	2010	41
15	Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations Human Mutation ·James J. Cox,Jony Sheynin,Zamir Shorer,Frank Reimann,Adeline K. Nicholas,Dominic F. Rodrigues,Marco Baralle,Elizabeth Wraige,Esther Manor,Jacov Levy,Crislyn Woods,Ruti Parvari	2010	84
16	WDR62 is associated with the spindle pole and is mutated in human microcephaly Nature Genetics ·Adeline K. Nicholas,李志欣,Julie Désir,Ofélia P. Carvalho,James J. Cox,Saigusa Shigeru,Rizwana Kausar,Muhammad Ansar,Wasim Ahmad,Alain Verloès,Sandrine Passemard,Jee-Sun Nam,Susan Lindsay,Fanni Gergely,William B. Dobyns,Emma Roberts,Marc Abramowicz,C. Geoffrey Woods	2010	211
17	Two novel SCN9A mutations causing insensitivity to pain Pain ·Kristian Bernhard Nilsen,Adeline K. Nicholas,C. Geoffrey Woods,Svein Ivar Mellgren,Erla Mari Bombín Gómez,Jan Aasly	2009	78
18	Absence of pain with hyperhidrosis: A new syndrome where vascular afferents may mediate cutaneous sensation Pain ·David Bowsher,Geoffrey Woods,Adeline K. Nicholas,Joshua Jay,Viktoriya V. Krupskaya,A. Lama,J. M. MacKenzie,Daniel Crooks,S Reichert,Thais Benites Fernandes Rosa,Hector Emmanuel Hernández,浩介矢箆原,James Wymer,Phillip J. Albrecht,Charles E. Argoff,Frank L. Rice	2009	25
19	The molecular landscape of ASPM mutations in primary microcephaly Journal of Medical Genetics ·Adeline K. Nicholas,Eric A. Swanson,James J. Cox,Gulshan Karbani,Mitun Aghipothu Umashankar,Kelly Springell,Daniel J. Hampshire,M Ahmed,Jacquelyn Bond,Daniela Benedetto,Marco Fichera,Corrado Romano,William B. Dobyns,C. Geoffrey Woods	2008	68
20	An SCN9A channelopathy causes congenital inability to experience painbreakdown → Nature ·James J. Cox,Frank Reimann,Adeline K. Nicholas,Saigusa Shigeru,Emma Roberts,Kelly Springell,Gulshan Karbani,Hussain Jafri,侯业智,Yasmin Raashid,Lihadh Al‐Gazali,O. P. Dragan,Enza Maria Valente,Shaun Gorman,Richard Williams,Duncan P. McHale,John N. Wood,Fiona M. Gribble,C. Geoffrey Woods	2006	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), Ion channel regulation and function (5 papers), Congenital heart defects research (4 papers), Genetic Syndromes and Imprinting (3 papers), Neonatal Respiratory Health Research (3 papers), Microtubule and mitosis dynamics (3 papers) and Growth Hormone and Insulin-like Growth Factors (3 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 Genetics, Journal of Medical Genetics, Pain, Thyroid and Clinical Endocrinology.

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