D. Lindhout

W. Arts, J. Oosterwijk, D. Lindhout, 2002, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K17I ANG MUTATION

R. Ophoff, F. Baas, F. Diekstra, 2009, Neurology.

Male patients affected by mosaic PCDH19 mutations: five new cases

G. Mancini, P. Rump, D. Lindhout, 2017, neurogenetics.

Etiologies for Seizures Around the Time of Vaccination

D. Lindhout, F. Jansen, N. Knoers, 2014, Pediatrics.

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.

C. Baker, H. Mefford, E. Eichler, 2010, Brain : a journal of neurology.

Copy Number Variations in Patients With Electrical Status Epilepticus in Sleep

M. Poot, D. Lindhout, F. Jansen, 2012, Journal of child neurology.

Epilepsy treatment: precision medicine at a crossroads

D. Lindhout, 2015, The Lancet Neurology.

Erratum: Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy (Epilepsia (2013) 54 (256-264) DOI:10.1111/epi.12517)

H. Mefford, C. Elger, A. Scabar, 2013 .

Seizure precipitants in Dravet syndrome: What events and activities are specifically provocative compared with other epilepsies?

F. Leijten, D. Lindhout, F. Jansen, 2015, Epilepsy & Behavior.

Prevalence of SCN1A-Related Dravet Syndrome among Children Reported with Seizures following Vaccination: A Population-Based Ten-Year Cohort Study

D. Lindhout, F. Jansen, E. Brilstra, 2013, PloS one.

Declining malformation rates with changed antiepileptic drug prescribing

T. Tomson, E. Perucca, D. Lindhout, 2019, Neurology.

Cancer risk in Peutz‐Jeghers syndrome

D. Lindhout, J. Wilson, G. Offerhaus, 1998 .

Epidemiology, pathophysiology and putative genetic basis of carbamazepine‐ and oxcarbazepine‐induced hyponatremia

J. Sander, D. Lindhout, B. Koeleman, 2016, European journal of neurology.

Different phenotypic expression in relatives with fabry disease caused by a W226X mutation.

D. Lindhout, B. Poll-The, M. Ausems, 1999, American journal of medical genetics.

An Arg for Gly substitution at position 31 in the insulin receptor, linked to insulin resistance, inhibits receptor processing and transport.

D. Lindhout, W. Möller, J. Maassen, 1992, The Journal of biological chemistry.

Gestation-induced changes in lamotrigine pharmacokinetics: A monotherapy study

M. Engelsman, D. Lindhout, G. de Haan, 2004, Neurology.

Effect of vaccinations on seizure risk and disease course in Dravet syndrome

H. Stroink, D. Lindhout, F. Jansen, 2015, Neurology.

Molecular characterization of WFS1 in patients with Wolfram syndrome.

C. Cremers, J. Maassen, D. Lindhout, 2003, The Journal of molecular diagnostics : JMD.

A pre-visit tailored website enhances counselees’ realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling

J. Bensing, S. Dulmen, D. Lindhout, 2012, Familial Cancer.

THE POLYCYSTIC KIDNEY-DISEASE-1 GENE ENCODES A 14-KB TRANSCRIPT AND LIES WITHIN A DUPLICATED REGION ON CHROMOSOME-16

Siep Thomas, S. Verhoef, J. Hughes, 1994 .

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

A. Kelemen, W. Arts, D. Lindhout, 2013, neurogenetics.

Is hearing loss a feature of Joubert syndrome, a ciliopathy?

D. Lindhout, B. Poll-The, M. S. van der Knaap, 2010, International journal of pediatric otorhinolaryngology.

Antiepileptic drugs and teratogenesis in two consecutive cohorts: changes in prescription policy paralleled by changes in pattern of malformations.

H. Nau, D. Lindhout, H. Meinardi, 1992, Neurology.

Ring chromosome 20 epilepsy syndrome in children

W. van Emde Boas, D. Lindhout, C. Wouters, 2001, Neurology.

Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia

D. Lindhout, R. Snijder, J. Mager, 2005, Journal of Medical Genetics.

Pregnancy and the Risk of Teratogenicity

D. Lindhout, J. Omtzigt, 1992, Epilepsia.

High rate of mosaicism in tuberous sclerosis complex.

S. Verhoef, A. V. D. van den Ouweland, D. Lindhout, 1999, American journal of human genetics.

Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies

Michael R. Johnson, I. Scheffer, D. Goldstein, 2014, The Lancet Neurology.

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

Christian E Elger, Holger Lerche, Ulrich Stephani, 2009, Nature Genetics.

DNA-based prenatal diagnosis for very-long- chain acyl-CoA dehydrogenase deficiency

L. D. Schroeder, L. Bolund, R. Wanders, 1999, Journal of Inherited Metabolic Disease.

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

C. Gieger, I. Scheffer, T. Wienker, 2012, Human molecular genetics.

Ventricular septal defect with overriding aorta in trisomy-18

D. Lindhout, R. J. Moene, M. Sobotka-Plojhar, 1988, European Journal of Pediatrics.

A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP‐glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler‐Najjar type IIs

Jurgen Seppen, P. Bosma, J. Seppen, 1996, FEBS letters.

Lamotrigine kinetics within the menstrual cycle, after menopause, and with oral contraceptives

D. Lindhout, P. Edelbroek, S. Bulk, 2009, Neurology.

Effect of oral contraceptives on lamotrigine levels depends on comedication

Josemir W Sander, D. Lindhout, A. J. Wilhelm, 2014, Acta neurologica Scandinavica.

The impact of age on lamotrigine and oxcarbazepine kinetics: A historical cohort study

Josemir W Sander, D. Lindhout, A. J. Wilhelm, 2013, Epilepsy & Behavior.

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.

D Lindhout, P. Bosma, B. Oostra, 1995, The New England journal of medicine.

Antiepileptic drugs and intrauterine death

T. Tomson, E. Perucca, D. Lindhout, 2015, Neurology.

Dose-dependent risk of malformations with antiepileptic drugs: an analysis of data from the EURAP epilepsy and pregnancy registry

T. Tomson, E. Perucca, D. Lindhout, 2011, The Lancet Neurology.

Drug monitoring of lamotrigine and oxcarbazepine combination during pregnancy

Josemir W Sander, D. Lindhout, G. de Haan, 2010, Epilepsia.

Seizure control and treatment in pregnancy

S. Kochen, M. Bacher, B. Steinhoff, 2006, Neurology.

Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

A. Hofman, D. Grobbee, V. Hiilesmaa, 1997, Epilepsia.

Seizure control and treatment changes in pregnancy: Observations from the EURAP epilepsy pregnancy registry

T. Tomson, E. Perucca, D. Lindhout, 2013, Epilepsia.

EURAP: An International Registry of Antiepileptic Drugs and Pregnancy

T. Tomson, E. Perucca, D. Lindhout, 2004, Epilepsia.

Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry

S. Kochen, A. Carius, B. Steinhoff, 2018, The Lancet Neurology.

Antiepileptic drug regimens and major congenital abnormalities in the offspring

A. Hofman, C. V. van Duijn, D. Lindhout, 1999, Annals of neurology.

A genome‐wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine

Michael R. Johnson, Josemir W Sander, H. Stefánsson, 2019, Epilepsia open.

Teratogenicity of Antiepileptic Drug Combinations with Special Emphasis on Epoxidation (of Carbamazepine)

D. Lindhout, H. Meinardi, R. Höppener, 1984, Epilepsia.

University of Groningen Mutations in WNT 10 A are present in more than half of isolated hypodontia cases

D. Lindhout, Y. Bronkhorst, M. Cune, 2017 .

Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

Colin A. Johnson, M. Hurles, D. Bonthron, 2013, Nature Genetics.

Application of chromosome 16 markers in the differential diagnosis of neuronal ceroid-lipofuscinosis.

C. Catsman-Berrevoets, D. Lindhout, M. Breuning, 1995, American journal of medical genetics.

The Pena-Shokeir syndrome: report of nine Dutch cases.

D. Lindhout, G. Hageman, F. Beemer, 1985, American journal of medical genetics.

Identification and characterization of the tuberous sclerosis gene on chromosome 16

S. Thomas, S. Verhoef, B. Janssen, 1993, Cell.

Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies

I. Scheffer, C. Elger, S. Lorenz, 2006, Epilepsia.

Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.

Joshua L. Deignan, T. Bourgeron, R. Delorme, 2019, American journal of human genetics.

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

W. Arts, J. V. van Harssel, D. Lindhout, 2013, neurogenetics.

The diagnostic management of newborns with congenital contractures: a nosologic study of 75 cases.

D. Lindhout, G. Hageman, F. Beemer, 1988, American journal of medical genetics.

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2).

R. Michelucci, S. Berkovic, J. Serratosa, 1999, Human molecular genetics.

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Dennis E Bulman, Ronald van Eijk, Peter J Oefner, 1996, Cell.

Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood

S. Verhoef, A. V. D. van den Ouweland, D. Lindhout, 1999, European Journal of Pediatrics.

Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis

R. Sinke, H. Scheffer, D. Lindhout, 2002, Neurology.

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Christian Gieger, Norman Delanty, Ellen Campbell, 2018, Nature Communications.

Advancing the phenome alongside the genome in epilepsy studies

Ingo Helbig, I. Helbig, D. Lindhout, 2017, Neurology.

Nav1.1 dysfunction in genetic epilepsy with febrile seizures‐plus or Dravet syndrome

Alfred L George, H. Stroink, A. George, 2011, The European journal of neuroscience.

Endophenotype Strategy in Epilepsy Genetics

D. Pinto, D. Lindhout, D. Trenité, 2009 .

ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies

S. Berkovic, J. Serratosa, R. Ottman, 2002 .

ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies

K. Lindblad-Toh, M. Leppert, J. Ott, 2002, Epilepsia.

A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23 a

J. Haines, J. Attwood, S. Povey, 1991, Annals of the New York Academy of Sciences.

Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome

D. Lindhout, F. Visscher, S. Drop, 2002, Journal of medical genetics.

Neurocognition after prenatal levetiracetam, lamotrigine, carbamazepine or valproate exposure

F. Oort, D. Lindhout, Roos Rodenburg, 2020, Journal of Neurology.

Familial Partial Epilepsy with Variable Foci in a Dutch Family: Clinical Characteristics and Confirmation of Linkage to Chromosome 22q

J. Hottenga, L. Sandkuijl, D. Lindhout, 2003, Epilepsia.

Management of prenatally detected trisomy 8 mosaicism

D. Lindhout, M. Haelst, D. Van Opstal, 2001, Prenatal diagnosis.

Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly

D. Lindhout, A. Palan, K. Madan, 1987, Human Genetics.

Familial endometrial cancer in female carriers of MSH6 germline mutations

P. Møller, H. Meijers-Heijboer, R. Hofstra, 1999, Nature Genetics.

Well-being of mothers with epilepsy with school-aged children

F. Oort, D. Lindhout, Roos Rodenburg, 2020, Epilepsy & Behavior.

Frequently asked questions on epilepsy, pregnancy and lactation: A EURAP-NL report

D. Lindhout, A. E. Rapcencu, S. Bulk, 2012, Seizure.

Adult patients with spina bifida cystica: genetic counselling, pregnancy and delivery

D. Lindhout, C. C. Rietberg, C. Rietberg, 1993 .

A pre-visit tailored website enhances counselees’ realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling

S. van Dulmen, J. Bensing, S. Dulmen, 2011, Familial Cancer.

Mutations in ACTL 6 B cause neurodevelopmental deficits and epilepsy and lead to 1 loss of dendrites in human neurons 2 3

Anne, Fassi, Joshua L. Deignan, 2019 .

Possible role of the innate immunity in temporal lobe epilepsy

M. G. Koerkamp, F. Holstege, P. V. van Rijen, 2008, Epilepsia.

Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumb.

H. Venema, E. Gelsema, S. Hovius, 1997, Journal of medical genetics.

Phenotypic analysis of triphalangeal thumb and associated hand malformations.

P. Heutink, B. Oostra, S. Hovius, 1994, Journal of medical genetics.

Inheritance of cranio-fronto-nasal syndrome.

D. Lindhout, M. Kwee, 1988, American journal of medical genetics.

The 10,11‐Epoxide‐10,11‐diol Pathway of Carbamazepine in Early Pregnancy in Maternal Serum, Urine, and Amniotic Fluid: Effect of Dose, Comedication, and Relation to Outcome of Pregnancy

D. Lindhout, J. Meijer, F. Los, 1993, Therapeutic drug monitoring.

DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands.

M. Nelen, R. Sinke, D. Lindhout, 2008, European journal of medical genetics.

Prenatal ultrasonographic diagnosis of radial‐ray reduction malformations

J. Wladimiroff, C. Meijer, H. V. van Geijn, 1990, Prenatal diagnosis.

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

R. Ophoff, H. Diener, M. Ferrari, 1995, Human Genetics.

Frontonasal dysplasia, coronal cranisoynostosis, pre‐ and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression?

D. Lindhout, M. Kwee, 1983, Clinical genetics.

Analysis of TSC2 stop codon variants found in tuberous sclerosis patients

A. Ouweland, S. Verhoef, M. Goedbloed, 2001, European Journal of Human Genetics.

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q

Jean Weissenbach, Peter Heutink, Ben A. Oostra, 1994, Nature Genetics.

Fibrodysplasia ossificans progressiva: current concepts and the role of CT in acute changes

R. Golding, D. Lindhout, A. Taets van Amerongen, 2006, Pediatric Radiology.

Concordant cerebral oligodendroglioma in identical twins.

W. Kamphorst, D. Lindhout, N. Roelvink, 1986, Journal of neurology, neurosurgery, and psychiatry.

Short report Concordant cerebral oligodendroglioma in identical twins

W. Kamphorst, D. Lindhout, N. Roelvink, 2004 .

Craniofrontonasal dysplasia: Genetic heterogeneity?

D. Lindhout, M. Kwee, 1984, Clinical genetics.

Study protocol of a Dutch prospective observational study into fetal Antiepileptic Drug exposure and long-term neurocognitive, behavioral and family outcomes Huber-Mollema,

F. Oort, D. Lindhout, Roos Rodenburg, 2018 .

Male patients affected by mosaic PCDH19 mutations: five new cases

P. Rump, D. Lindhout, M. Kriek, 2017, neurogenetics.

Genome‐wide linkage meta‐analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

I. Scheffer, C. Elger, R. Kaneva, 2012, Epilepsia.

Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis

D. Pinto, I. Scheffer, P. Striano, 2010, Epilepsy Research.

Oligogenic inheritance in photosensitive juvenile myoclonic epilepsy?

D. Pinto, D. Lindhout, B. Koeleman, 2006, Epileptic disorders : international epilepsy journal with videotape.

Evidence for Linkage between Juvenile Myoclonic Epilepsy–Related Idiopathic Generalized Epilepsy and 6p11‐12 in Dutch Families

D. Pinto, D. Lindhout, D. Halley, 2004, Epilepsia.

Brief Communication ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies ILAE Genetics Commission

K. Lindblad-Toh, M. Leppert, J. Ott, 2002 .

Identification of Srp9 as a febrile seizure susceptibility gene

A. A. Kan, F. Holstege, C. Hoogenraad, 2014, Annals of clinical and translational neurology.

Favourable mutation test outcomes for individuals at risk for Huntington disease change the perspectives of first-degree relatives

T. Stijnen, B. Bonke, D. Lindhout, 2002, Human Genetics.

Fetal methotrexate syndrome: A systematic review of case reports.

D. Lindhout, J. P. van Tintelen, M. V. van Haelst, 2019, Reproductive toxicology.

Reduced bilirubin UDP-glucuronosyltransferase expression in Gilbert syndrome is caused by a sequence abnormality in the promoter region

P. Bosma, B. Oostra, G. Tytgat, 1996 .

Behavioral problems in children of mothers with epilepsy prenatally exposed to valproate, carbamazepine, lamotrigine, or levetiracetam monotherapy

F. Oort, D. Lindhout, Roos Rodenburg, 2019, Epilepsia.

Using common genetic variants to find drugs for common epilepsies

David F. Smith, C. Gieger, I. Scheffer, 2021, Brain Communications.

MSH2 genomic deletions are a frequent cause of HNPCC

P. Møller, D. Lindhout, H. Vasen, 1998, Nature Genetics.

The disposition of valproate and its metabolites in the late first trimester and early second trimester of pregnancy in maternal serum, urine, and amniotic fluid: Effect of dose, co-medication, and the presence of spina bifida

H. Nau, D. Lindhout, F. Los, 1992, European Journal of Clinical Pharmacology.

Genetic aspects of polydactyly.

P. Heutink, B. Oostra, S. Hovius, 1996, Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V....

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

A. Cats, R. Fodde, R. Kolodner, 1996, American journal of human genetics.

A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease

P. Pearson, D. Lindhout, B. Poll-The, 2001, European Journal of Human Genetics.

Familial multiple epiphyseal dysplasia due to a matrilin‐3 mutation: Further delineation of the phenotype including 40 years follow‐up

P. Heutink, D. Lindhout, B. Jansen, 2003, American journal of medical genetics. Part A.

Bilateral hereditary micro-epiphyseal dysplasia: Further delineation of the phenotype with 40 years follow-up

P. Heutink, D. Lindhout, B. Jansen, 2002, International Orthopaedics.

Levetiracetam use and pregnancy outcome.

M. Engelsman, D. Lindhout, A. V. van Oppen, 2005, Reproductive toxicology.

A leucine‐to‐proline mutation in the insulin receptor in a family with insulin resistance.

L. Sandkuyl, D. Lindhout, W. Möller, 1989, The EMBO journal.

Genome search for susceptibility loci of common idiopathic generalised epilepsies.

T. Wienker, A. Sundquist, J. Prud'homme, 2000, Human molecular genetics.

Refined localization of TSC1 by combined analysis of 9q34 and 16pl3 data in 14 tuberous sclerosis families

S. Verhoef, L. Sandkuijl, B. Janssen, 1994, Human Genetics.

Genetic heterogeneity in tuberous sclerosis.

R. Hennekam, L. Sandkuyl, D. Lindhout, 1990, Genomics.

A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years

D. Pinto, M. Wapenaar, D. Lindhout, 2006, Epilepsia.

Partial Cosegregation of Familial Hemiplegic Migraine and a Benign Familial Infantile Epileptic Syndrome

L. Sandkuijl, D. Lindhout, R. Frants, 1997, Epilepsia.

Genetics of Photosensitivity (Photoparoxysmal Response): A Review

D. Pinto, U. Stephani, D. Lindhout, 2004, Epilepsia.

Neural tube defects associated with prenatal exposure to antiepileptic drugs

D. Lindhout, R. Galjaard, A. Oppen, 2007 .

Withdrawal of valproic acid treatment during pregnancy and seizure outcome: Observations from EURAP

T. Tomson, E. Perucca, D. Lindhout, 2016, Epilepsia.

Carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy

Josemir W Sander, D. Lindhout, J. van der Palen, 2017, Epilepsia.

Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients

D. Lindhout, R. Snijder, J. Mager, 2004, Human Genetics.

Univerricht‐Lundborg Disease: Underdiagnosed in the Netherlands

D. Lindhout, D. Halley, M. Majoie, 2004, Epilepsia.

Amyoplasia congenita-like condition and maternal malathion exposure.

D. Lindhout, G. Hageman, 1987, Teratology.

Complex cardiac defect with hypoplastic right ventricle in a fetus with valproate exposure

A. G. Gittenberger-de Groot, D. Lindhout, E. Brilstra, 2005, Prenatal diagnosis.

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

D. Lindhout, C. D. de Kovel, E. Brilstra, 2015, Neurotherapeutics.

Erratum to: Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

D. Lindhout, C. D. de Kovel, E. Brilstra, 2015, Neurotherapeutics.

Pharmacogenetics and drug interactions: role in antiepileptic-drug-induced teratogenesis.

D. Lindhout, 1992, Neurology.

Genetic Variability in Fetal Response to Anticonvulsants

D. Lindhout, 1989 .

Severe limb abnormalities: analysis of a cluster of five cases born during a period of 45 days.

D. Lindhout, J. N. van den Anker, T. Cohen-Overbeek, 1993, American journal of medical genetics.

The role of ultrasound in the early diagnosis of fetal structural defects following maternal anticonvulsant therapy.

D. Lindhout, J. Wladimiroff, P. Stewart, 1988, Ultrasound in medicine & biology.

Maternal epilepsy and behavioral development of the child: Family factors do matter

F. Oort, D. Lindhout, Roos Rodenburg, 2019, Epilepsy & Behavior.

Genome-wide Association Analysis of Genetic Generalized Epilepsies Implicates Susceptibility Loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 Epicure Consortium

C. Gieger, I. Scheffer, T. Wienker, 2022 .

Genotype–phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia

P. Zanen, D. Lindhout, R. Snijder, 2008, American journal of medical genetics. Part A.

CHAPTER 8 Familial partial epilepsy with variable foci in a Dutch family : clinical characteristics and confirmation of linkage to chromosome 22 q

D. Lindhout, R. Frants, J. Hottenga, 2006 .

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.

P. Devilee, R. Cornelis, D. Lindhout, 1993, American journal of human genetics.

Case 43 – Genetic Counseling in a Woman with a Family History of Refractory Myoclonic Epilepsy*

D. Lindhout, 2008 .

Symptomatology of carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy

Josemir W Sander, D. Lindhout, Anja C. M. Sonsma, 2021, Epilepsia.

Atypical Vitamin B6 Deficiency

U. Stephani, H. Muhle, R. Møller, 2014, Journal of child neurology.

Association Study of TRPC4 as a Candidate Gene for Generalized Epilepsy with Photosensitivity

J. Hampe, U. Stephani, H. Muhle, 2010, NeuroMolecular Medicine.

Explorative two‐locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures‐related photosensitivity loci

D. Pinto, K. Strauch, H. Cordell, 2007, Genetic epidemiology.

Hippocampal Navβ3 expression in patients with temporal lobe epilepsy

P. V. van Rijen, D. Lindhout, M. van Kempen, 2009, Epilepsia.

[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex].

S. Verhoef, A. V. D. van den Ouweland, D. Lindhout, 2001, Nederlands tijdschrift voor geneeskunde.

The Joubert syndrome associated with bilateral chorioretinal coloboma

D. Lindhout, P. Barth, R. Pfeiffer, 1981, European Journal of Pediatrics.

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

A. Zwinderman, K. Heimdal, P. Møller, 1998, The New England journal of medicine.

Erratum to: Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

D. Lindhout, E. Brilstra, B. Koeleman, 2015, Neurotherapeutics.

The Joubert Syndrome associated with bilateral chorioretinal coloboma

D. Lindhout, P. Barth, T. N. Boen-Tan, 1980, European Journal of Pediatrics.

Chorioretinal coloboma and Joubert syndrome.

D. Lindhout, P. Barth, 1985, The Journal of pediatrics.

Predicting adaptation to presymptomatic DNA testing for late onset disorders: who will experience distress? Rotterdam Leiden Genetics Workgroup.

Rotterdam, J. Passchier, H. Duivenvoorden, 1998, Journal of medical genetics.

A retrospective population‐based study on seizures related to childhood vaccination

I. Scheffer, U. Stephani, S. Berkovic, 2011 .

Genetics of limb development and congenital hand malformations.

P. Heutink, S. Hovius, D. Lindhout, 1998, Plastic and reconstructive surgery.

Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibships.

J. Wladimiroff, D. Lindhout, M. Niermeijer, 1989, American journal of medical genetics.

Epilepsy and mental retardation limited to females: an under-recognized disorder.

K. Friend, I. Scheffer, M. Shaw, 2008, Brain : a journal of neurology.

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, llq, and 12q

M. Pericak-Vance, Cardiff, S. Povey, 2022 .

Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations

D. Lindhout, E. Weber, A. Lehesjoki, 2005, European Journal of Human Genetics.

The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts

R. Sinke, D. Lindhout, R. Steegers-Theunissen, 2008, Human Genetics.

In search for genes predisposing to epilepsy: Motives and methods

D. Lindhout, T. Sander, D. Halley, 1992, Acta neurologica Scandinavica. Supplementum.

Benign familial neonatal convulsions

W. Arts, D. Lindhout, D. Halley, 1991, Clinical Neurology and Neurosurgery.

Prenatal analysis of insulin receptor autophosphorylation in a family with leprechaunism

J. Maassen, D. Lindhout, W. Kleijer, 1990, Prenatal Diagnosis.

Individuals with only one allele for a functional insulin receptor have a tendency to hyperinsulinaemia but not to hyperglycaemia

D. Lindhout, W. Möller, J. Maassen, 1989, Diabetologia.

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.

T. Wienker, J. Prud'homme, F. Zara, 2002, American journal of medical genetics.

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