Laura Yates

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Sally stephensNewcastle UniversityDirección de correo verificada de ncl.ac.uk
Amy O'DonnellProfessor of Applied Health & Social Care Research, Newcastle UniversityDirección de correo verificada de newcastle.ac.uk
Dorothy Newbury-BirchProfessor of Alcohol and Public Health ResearchDirección de correo verificada de tees.ac.uk
catherine nelson-piercyProfessor of OBSTETRIC MEDICINEDirección de correo verificada de gstt.nhs.uk
Luke ValeProfessor of Health Economics, LSHTMDirección de correo verificada de newcastle.ac.uk
Catherine McParlinSenior Resarch Midwife Newcastle upon Tyne Hospitals and Honorary Research Associate Newcastle UniversityDirección de correo verificada de ncl.ac.uk
Jill Clayton-SmithProfessor of Medical Genetics, University of Manchester, Clinical Geneticist, St Mary's Hospital, ManchesterDirección de correo verificada de cmft.nhs.uk
Alice PanchaudInstitute of Primary Care (BIHAM)Dirección de correo verificada de biham.unibe.ch
Thierry VialService HU de Pharmacotoxicologie, Directeur du CRPV deDirección de correo verificada de chu-lyon.fr
Louise HowardKing's College LondonDirección de correo verificada de kcl.ac.uk
John SayerProfessor of Renal MedicineDirección de correo verificada de ncl.ac.uk
Rebecca L BromleyUniversity of ManchesterDirección de correo verificada de manchester.ac.uk
Aileen MillProfessor of Modelling, Evidence and PolicyDirección de correo verificada de ncl.ac.uk
David BaudCHUVDirección de correo verificada de chuv.ch
Thierry BuclinCHUV and UNIL Lausanne (Switzewrland)Dirección de correo verificada de chuv.hospvd.ch
Mine Kadioglu DumanProf. Dr.Dirección de correo verificada de ktu.edu.tr
R Hamish McAllister-WilliamsNewcastle UniversityDirección de correo verificada de ncl.ac.uk
Carmine M. ParianteKing's College London, Institute of Psychiatry, Psychology and NeuroscienceDirección de correo verificada de kcl.ac.uk
Ian JonesCardiff UniversityDirección de correo verificada de cf.ac.uk
Maya TopfProfessor @ Centre for Structural Systems Biology - HamburgDirección de correo verificada de cssb-hamburg.de

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Laura Yates

newcastle

Dirección de correo verificada de newcastle.ac.uk

teratology medicines in pregnancy clinical genetics


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
Prevalence and architecture of de novo mutations in developmental disorders Nature 542 (7642), 433-438, 2017	880	2017
British Association for Psychopharmacology consensus guidance on the use of psychotropic medication preconception, in pregnancy and postpartum 2017 RH McAllister-Williams, DS Baldwin, R Cantwell, A Easter, E Gilvarry, ... Journal of Psychopharmacology 31 (5), 519-552, 2017	225	2017
Treatments for hyperemesis gravidarum and nausea and vomiting in pregnancy: a systematic review C McParlin, A O’Donnell, SC Robson, F Beyer, E Moloney, A Bryant, ... Jama 316 (13), 1392-1401, 2016	219	2016
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins RA Kumar, DT Pilz, TD Babatz, TD Cushion, K Harvey, M Topf, L Yates, ... Human molecular genetics 19 (14), 2817-2827, 2010	217	2010
Histone lysine methylases and demethylases in the landscape of human developmental disorders V Faundes, WG Newman, L Bernardini, N Canham, J Clayton-Smith, ... The American Journal of Human Genetics 102 (1), 175-187, 2018	205	2018
Cilia and disease L Eley, LM Yates, JA Goodship Current opinion in genetics & development 15 (3), 308-314, 2005	186	2005
Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle D Morgan, L Eley, J Sayer, T Strachan, LM Yates, AS Craighead, ... Human molecular genetics 11 (26), 3345-3350, 2002	185	2002
Influenza A/H1N1v in pregnancy: an investigation of the characteristics and management of affected women and the relationship to pregnancy outcomes for mother and infant L Yates, M Pierce, S Stephens, AC Mill, P Spark, JJ Kurinczuk, M Valappil, ... Health Technol Assess 14 (34), 109-82, 2010	167	2010
Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype LG Sadleir, EI Mountier, D Gill, S Davis, C Joshi, C DeVile, MA Kurian, ... Neurology 89 (10), 1035-1042, 2017	127	2017
Pregnancy outcomes following gabapentin use: results of a prospective comparative cohort study H Fujii, A Goel, N Bernard, A Pistelli, LM Yates, S Stephens, JY Han, ... Neurology 80 (17), 1565-1570, 2013	113	2013
Pregnancy outcome following maternal exposure to pregabalin may call for concern U Winterfeld, P Merlob, D Baud, V Rousson, A Panchaud, LE Rothuizen, ... Neurology 86 (24), 2251-2257, 2016	111	2016
Treatments for hyperemesis gravidarum and nausea and vomiting in pregnancy: a systematic review and economic assessment A O’Donnell, C McParlin, SC Robson, F Beyer, E Moloney, A Bryant, ... Health Technology Assessment 20 (74), vii-268, 2016	101	2016
Novel TMEM67 mutations and genotype‐phenotype correlates in meckelin‐related ciliopathies M Iannicelli, F Brancati, S Mougou‐Zerelli, A Mazzotta, S Thomas, ... Human mutation 31 (5), E1319-E1331, 2010	99	2010
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language L Snijders Blok, J Rousseau, J Twist, S Ehresmann, M Takaku, ... Nature communications 9 (1), 4619, 2018	96	2018
The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants K Tatton-Brown, A Zachariou, C Loveday, A Renwick, S Mahamdallie, ... Wellcome open research 3, 2018	85	2018
Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy AH O’Donnell-Luria, LS Pais, V Faundes, JC Wood, A Sveden, V Luria, ... The American Journal of Human Genetics 104 (6), 1210-1222, 2019	66	2019
Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative … L Lonie, DE Porter, M Fraser, T Cole, C Wise, L Yates, E Wakeling, E Blair, ... Human mutation 27 (11), 1160-1160, 2006	65	2006
Prescribing without evidence–pregnancy SHL Thomas, LM Yates British journal of clinical pharmacology 74 (4), 691-697, 2012	61	2012
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia KM Gorman, E Meyer, D Grozeva, E Spinelli, A McTague, A Sanchis-Juan, ... The American Journal of Human Genetics 104 (5), 948-956, 2019	58	2019
Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study JF McRae, S Clayton, TW Fitzgerald, J Kaplanis, E Prigmore, D Rajan, ... BioRxiv, 049056, 2016	51	2016

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