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Laura Yates
Laura Yates
Verified email at newcastle.ac.uk
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Year
Prevalence and architecture of de novo mutations in developmental disorders
Nature 542 (7642), 433-438, 2017
8782017
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
2252017
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
2192016
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
2172010
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
2042018
Cilia and disease
L Eley, LM Yates, JA Goodship
Current opinion in genetics & development 15 (3), 308-314, 2005
1862005
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
1852002
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
1672010
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
1272017
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
1132013
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
1112016
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
1012016
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
992010
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
962018
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
852018
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
652019
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
652006
Prescribing without evidence–pregnancy
SHL Thomas, LM Yates
British journal of clinical pharmacology 74 (4), 691-697, 2012
602012
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
582019
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
512016
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