Adele Dessa Sadovnick

Adele Dessa Sadovnick's AcademicInfluence.com Rankings

Biology

#10099

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#13392

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Neuroscience

#1528

World Rank

#1579

Historical Rank

biology Degrees

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Biology

Adele Dessa Sadovnick's Degrees

Bachelors Biology University of California, Berkeley
PhD Neuroscience Stanford University

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Adele Dessa Sadovnick's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 (2006) (1809)
Sex ratio of multiple sclerosis in Canada: a longitudinal study (2006) (857)
A full genome search in multiple sclerosis (1996) (709)
A genetic basis for familial aggregation in multiple sclerosis (1995) (674)
A population-based study of multiple sclerosis in twins. (1986) (638)
Vascular Factors and Risk of Dementia: Design of the Three-City Study and Baseline Characteristics of the Study Population (2003) (617)
Vitamin D intake and incidence of multiple sclerosis (2004) (507)
Expression of the Multiple Sclerosis-Associated MHC Class II Allele HLA-DRB1*1501 Is Regulated by Vitamin D (2009) (505)
Twin concordance and sibling recurrence rates in multiple sclerosis (2003) (502)
Timing of birth and risk of multiple sclerosis: population based study (2004) (461)
Head injury and the risk of AD in the MIRAGE study (2000) (456)
A population‐based study of multiple sclerosis in twins: Update (1993) (421)
Cause of death in patients attending multiple sclerosis clinics (1991) (395)
Evidence for genetic basis of multiple sclerosis (1996) (377)
Disclosure of APOE genotype for risk of Alzheimer's disease. (2009) (376)
Multiple sclerosis: updated risks for relatives. (1988) (355)
Depression and multiple sclerosis (1996) (346)
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis (2005) (345)
Epidemiology of Multiple Sclerosis: A Critical Overview (1993) (325)
Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder (2006) (300)
Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study (1996) (288)
A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22. (2001) (283)
Diagnosis and treatment of dementia: 1. Risk assessment and primary prevention of Alzheimer disease (2008) (266)
Parent-of-origin effect in multiple sclerosis: observations in half-siblings (2004) (265)
Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis23 (2008) (248)
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. (2005) (240)
Genetics of multiple sclerosis (2004) (226)
Genetics of multiple sclerosis. (1995) (211)
Screening for PS1 mutations in a referral-based series of AD cases (2001) (203)
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis (2008) (203)
Early-Onset Familial Alzheimer's Disease (EOFAD) (2012) (181)
Familiality of temperament in bipolar disorder: support for a genetic spectrum. (2005) (179)
Phenotypic heterogeneity in familial alzheimer's disease: A study of 24 kindreds (1989) (172)
Life expectancy in patients attending multiple sclerosis clinics (1992) (171)
Life expectancy in Down syndrome. (1987) (170)
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia. (2001) (169)
MRI parameters for prediction of multiple sclerosis diagnosis in children with acute CNS demyelination: a prospective national cohort study (2011) (162)
Estimating risk curves for first-degree relatives of patients with Alzheimer’s disease: The REVEAL study (2004) (161)
Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility (2009) (155)
Conjugal multiple sclerosis: Population‐based prevalence and recurrence risks in offspring (2000) (154)
Apolipoprotein E ε4 genotype as a risk factor for cognitive decline and dementia: data from the Canadian Study of Health and Aging (2004) (153)
Autoimmune disease in families with multiple sclerosis: a population-based study (2007) (150)
Evidence for linkage disequilibrium between the dopamine transporter and bipolar disorder. (2001) (148)
The Inheritance of Resistance Alleles in Multiple Sclerosis (2007) (138)
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus (2007) (136)
LIFE EXPECTANCY IN DOWN SYNDROME ADULTS (1988) (132)
2010 McDonald criteria for diagnosing pediatric multiple sclerosis (2012) (130)
The geographic distribution of multiple sclerosis: a review. (1993) (126)
Canadian Collaborative Project on Genetic Susceptibility to MS, Phase 2: Rationale and Method (1998) (125)
School-based hepatitis B vaccination programme and adolescent multiple sclerosis (2000) (125)
Maternal age and birth defects: a population study (1991) (117)
The natural history of multiple sclerosis: a geographically based study: 8: familial multiple sclerosis. (2000) (114)
Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group. (1996) (113)
Who seeks genetic susceptibility testing for Alzheimer’s disease? Findings from a multisite, randomized clinical trial (2004) (112)
Possible locus for bipolar disorder near the dopamine transporter on chromosome 5. (1996) (112)
Clinical features of children and adolescents with multiple sclerosis (2007) (112)
Risks of multiple sclerosis in relatives of patients in Flanders, Belgium. (1997) (109)
Evidence that a single nucleotide polymorphism in the promoter of the G protein receptor kinase 3 gene is associated with bipolar disorder (2003) (109)
Pregnancy and multiple sclerosis. A prospective study. (1994) (103)
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17. (2006) (102)
Linkage studies suggest a possible locus for bipolar disorder near the velo-cardio-facial syndrome region on chromosome 22. (1997) (101)
Prevalence of Multiple Sclerosis in British Columbia (1986) (99)
Concurrence of multiple sclerosis and inflammatory bowel disease. (1989) (97)
The familial nature of multiple sclerosis (1981) (96)
Association of Infectious Mononucleosis with Multiple Sclerosis (2009) (96)
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease. (1991) (95)
Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex. (2008) (94)
Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients (2000) (93)
Multiple sclerosis in stepsiblings: recurrence risk and ascertainment (2006) (91)
HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility (2008) (91)
Parent‐child concordance in multiple sclerosis (1991) (90)
The familial nature of multiple sclerosis (1988) (87)
Prevalence of multiple sclerosis. (1982) (86)
Sibling risks of abdominal aortic aneurysm (1995) (85)
Age of puberty and the risk of multiple sclerosis: a population based study (2009) (80)
Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis. (2001) (78)
Depressive symptoms and family history in seasonal and nonseasonal mood disorders. (1993) (77)
Age at Onset of Multiple Sclerosis May Be Influenced by Place of Residence during Childhood Rather than Ancestry (2006) (77)
Reproductive decision making after the diagnosis of multiple sclerosis (MS) (2013) (77)
Apolipoprotein E epsilon4 genotype as a risk factor for cognitive decline and dementia: data from the Canadian Study of Health and Aging. (2004) (76)
Epidemiology of multiple sclerosis. (2011) (76)
Risk alleles for multiple sclerosis in multiplex families (2009) (73)
Age of onset in siblings concordant for multiple sclerosis. (1991) (73)
Parent-of-origin effects in MS (2008) (72)
Causes of death to age 30 in Down syndrome. (1988) (70)
Vitamin D metabolic pathway genes and risk of multiple sclerosis in Canadians (2011) (69)
DNA length polymorphism 5′ to the myelin basic protein gene is associated with multiple sclerosis (1990) (68)
Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative Study (2009) (66)
An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. (2004) (65)
Epidemiology and genetics of multiple sclerosis. (1992) (65)
Nuclear Receptor NR1H3 in Familial Multiple Sclerosis (2016) (64)
Genetic background of multiple sclerosis. (2012) (64)
Sex ratio of multiple sclerosis and clinical phenotype (2010) (62)
A timing-of-birth effect on multiple sclerosis clinical phenotype (2007) (61)
European Charcot Foundation Lecture: The natural history of multiple sclerosis and gender (2009) (61)
HLA-DRB1 confers increased risk of pediatric-onset MS in children with acquired demyelination (2011) (60)
Evaluation of late-onset Alzheimer disease genetic susceptibility risks in a Canadian population (2014) (59)
Effect of age at onset and parental disease status on sibling risks for MS (1998) (57)
HLA-DRB1 and month of birth in multiple sclerosis (2009) (56)
Characterizing neuropsychiatric symptoms in subjects referred to dementia clinics (2006) (56)
Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene (2012) (56)
PRKCA and Multiple Sclerosis: Association in Two Independent Populations (2006) (55)
Bipolar disorder: evidence for a major locus. (1995) (55)
Multiple sclerosis and birth order: a longitudinal cohort study (2005) (54)
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease (2019) (54)
Perinatal outcomes in women with multiple sclerosis exposed to disease-modifying drugs (2012) (53)
No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study (2002) (53)
Genetic counselling in multiple sclerosis: risks to sibs and children of affected individuals (1999) (53)
Mood Disorder Service Genetic Database: morbidity risks for mood disorders in 3,942 first-degree relatives of 671 index cases with single depression, recurrent depression, bipolar I, or bipolar II. (1994) (52)
Genetic epidemiology of multiple sclerosis: A survey (1994) (52)
MHC transmission (2011) (51)
Parental transmission of HLA-DRB1*15 in multiple sclerosis (2007) (50)
Life tables for Down syndrome (1989) (50)
Segmental linkage disequilibrium within the dopamine transporter gene (2002) (50)
Association of smoking with risk of multiple sclerosis: a population-based study (2013) (48)
Parental transmission of MS in a population-based Canadian cohort (2007) (47)
CONCORDANCE IN TWINS AND RECURRENCE IN SIBSHIPS IN MULTIPLE SCLEROSIS (1982) (46)
Genetics of multiple sclerosis. (1995) (46)
Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium. (2007) (44)
Maternal age-specific rates for Down syndrome: changes over time. (1988) (42)
Genetic linkage study of bipolar disorder and the serotonin transporter. (1996) (42)
Viral exposures and MS outcome in a prospective cohort of children with acquired demyelination (2016) (42)
Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis. (2010) (42)
The Canadian survey of health, lifestyle and ageing with multiple sclerosis: methodology and initial results (2014) (41)
Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosis (2017) (41)
A cost-benefit analysis of prenatal detection of Down syndrome and neural tube defects in older mothers. (1981) (39)
Genomewide study of multiple sclerosis. (2007) (38)
Mental retardation in over half-a-million consecutive livebirths: an epidemiological study. (1985) (38)
Genetics and dementia: Risk factors, diagnosis, and management (2007) (37)
Examination of the clock gene Cryptochrome 1 in bipolar disorder: mutational analysis and absence of evidence for linkage or association (2005) (36)
Association between microchimerism and multiple sclerosis in Canadian twins (2006) (36)
Evaluating the parent-of-origin effect in bipolar affective disorder. Is a more penetrant subtype transmitted paternally? (2000) (36)
Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progression (2014) (35)
Maternal age and oral cleft malformations: data from a population-based series of 576,815 consecutive livebirths. (1994) (34)
Temporal changes in the utilization of amniocentesis for prenatal diagnosis by women of advanced maternal age, 1976–1983 (1985) (34)
Birth hospitalization in mothers with multiple sclerosis and their newborns (2013) (34)
Linkage of a bipolar disorder susceptibility locus to human chromosome 13q32 in a new pedigree series (2003) (33)
Familial recurrence risks and inheritance of multiple sclerosis. (1993) (33)
Suggestive linkage of a chromosomal locus on 18p11 to cyclothymic temperament in bipolar disorder families (2008) (33)
A genome-wide scan in forty large pedigrees with multiple sclerosis (2007) (32)
A multigenerational family with multiple sclerosis. (2002) (32)
Clinical and MRI activity as determinants of sample size for pediatric multiple sclerosis trials (2013) (31)
Heritability and genome-wide SNP linkage analysis of temperament in bipolar disorder. (2013) (31)
The interaction of MS and pregnancy: a critical review. (2003) (31)
Safety of disease-modifying drugs for multiple sclerosis in pregnancy: current challenges and future considerations for effective pharmacovigilance (2013) (30)
A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease (2015) (30)
Genetic studies on an Alzheimer Clinic population (1989) (29)
Obstetrical epidural and spinal anesthesia in multiple sclerosis (2013) (28)
Major depression, minor depression, and double depression: are they distinct clinical entities? (1996) (27)
Age of Onset in Concordant Twins and Other Relative Pairs With Multiple Sclerosis (2009) (27)
Congenital malformations associated with anencephaly in liveborn and stillborn infants. (1985) (27)
Correlation of IQ in subjects with Down syndrome and their parents and sibs. (2008) (26)
Orientation Dependent MR Signal Decay Differentiates between People with MS, Their Asymptomatic Siblings and Unrelated Healthy Controls (2015) (26)
A Review of Safety-Related Pregnancy Data Surrounding the Oral Disease-Modifying Drugs for Multiple Sclerosis (2014) (26)
Nuclear Receptor NR1H3 in Familial Multiple Sclerosis (2016) (26)
The need for a disease-specific prospective pregnancy registry for multiple sclerosis (MS). (2015) (26)
Multiple sclerosis in the Iranian immigrant population of BC, Canada: prevalence and risk factors (2014) (26)
Increased mean R2* in the deep gray matter of multiple sclerosis patients: Have we been measuring atrophy? (2018) (25)
No evidence for an effect of DNA methylation on multiple sclerosis severity at HLA-DRB1*15 or HLA-DRB5 (2010) (24)
Ethical Guidelines of the Alzheimer Society of Canada (1998) (24)
An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene (2009) (23)
A genome scan in a single pedigree with a high prevalence of multiple sclerosis (2007) (22)
TRPV1 Gates Tissue Access and Sustains Pathogenicity in Autoimmune Encephalitis (2013) (22)
Masquerades of Acquired Demyelination in Children (2013) (21)
A comparison of incidence trends for esophageal atresia and tracheoesophageal fistula, and infectious disease. (1987) (21)
Familial risks for Alzheimer disease from a population‐based series (1994) (21)
Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis (2008) (21)
Reproductive counselling for MS: a rationale. (2003) (21)
Is sporadic MS caused by an infection of adolescence and early adulthood? A case‐control study of birth order position (1995) (21)
A study of birth order and multiple sclerosis in multiplex families. (1995) (20)
Parent-of-origin of HLA-DRB1*1501 and age of onset of multiple sclerosis (2009) (20)
Vitamin D intake and incidence of multiple sclerosis [1] (multiple letters) (2004) (20)
Effects of infectious mononucleosis and HLA-DRB1*15 in multiple sclerosis (2010) (20)
Analysis of CYP27B1 in multiple sclerosis (2014) (19)
Birth outcomes of pregnancies fathered by men with multiple sclerosis (2013) (19)
Methylation of class II transactivator gene promoter IV is not associated with susceptibility to Multiple Sclerosis (2008) (19)
Prevalence of MS in Iranian Immigrants to British Columbia, Canada (2010) (19)
Genetic modifiers of multiple sclerosis progression, severity and onset. (2017) (19)
Reproductive counselling in MS: a guide for healthcare professionals. (2003) (19)
Familial Alzheimer's Disease (1988) (18)
Differential effects of genetic susceptibility factors in males and females with multiple sclerosis. (2013) (18)
Association of dopamine transporter gene variants with childhood ADHD features in bipolar disorder (2013) (18)
NLRX1 inhibits the early stages of CNS inflammation and prevents the onset of spontaneous autoimmunity (2019) (18)
Season of birth in multiple sclerosis (1994) (17)
A cost-benefit analysis of prenatal diagnosis for neural tube defects selectively offered to relatives of index cases. (1982) (17)
Population-based study of long-term outcomes after amniocentesis (1994) (17)
A cost‐benefit analysis of a population screening programme for neural tube defects (1983) (17)
Safety and efficacy of venoplasty in MS (2018) (17)
Variants in the promoter region of CYP7A1 are associated with neuromyelitis optica but not with multiple sclerosis in the Han Chinese population (2013) (17)
Genetic Counseling for Early-onset Familial Alzheimer Disease in Large Aboriginal Kindred from a Remote Community in British Columbia: Unique Challenges and Possible Solutions (2011) (16)
The role of hereditary spastic paraplegia related genes in multiple sclerosis (2007) (16)
Issues in Molecular Genetic Testing of Individuals with Suspected Early‐onset Familial Alzheimer's Disease (1994) (16)
Mutations in the hemochromatosis gene and the clinical outcome of multiple sclerosis (2008) (16)
The influence of gender on the susceptibility to multiple sclerosis in sibships. (1991) (16)
Interferon beta babies (2005) (16)
Follow-up investigation of 12 proposed linkage regions in multiple sclerosis (2006) (15)
Erratum: Genetics of multiple sclerosis (Human Molecular Genetics (1997) 6 (1693-1698)) (1997) (14)
Analysis of NOD-like receptor NLRP1 in multiple sclerosis families (2018) (14)
The LRRK2 R1628P Variant Plays a Protective Role in Han Chinese Population with Alzheimer's Disease (2013) (14)
Case-Control Studies Are Not Familial Studies (2016) (14)
The impact of resilience on healthy aging with multiple sclerosis (2020) (14)
A linkage disequilibrium study of bipolar disorder and microsatellite markers on 22q13 (2002) (14)
Heterogeneity in Multiple Sclerosis: Comparison of Clinical Manifestations in Relatives (1990) (14)
No effect of preterm birth on the risk of multiple sclerosis: a population based study (2008) (14)
Suggestive evidence for linkage of ADHD features in bipolar disorder to chromosome 10p14 (2009) (14)
Common genetic etiology between “multiple sclerosis-like” single-gene disorders and familial multiple sclerosis (2017) (14)
Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination (2011) (13)
No Effect of Birth Weight on the Risk of Multiple Sclerosis (2008) (13)
Analysis of CH25H in multiple sclerosis and neuromyelitis optica (2016) (13)
Childhood cow's milk allergy and the risk of multiple sclerosis: A population based study (2010) (13)
Incidence of Multiple Sclerosis and Related Disorders in Asian Populations of British Columbia (2015) (13)
Multiple Sclerosis and Pregnancy: Maternal Considerations (2012) (13)
HLA-DRB1 AND MULTIPLE SCLEROSIS IN MALTA (2008) (13)
Association Between Alzheimer Disease and Amyotrophic Lateral Sclerosis? (1990) (12)
Birth Outcomes in Newborns Fathered by Men with Multiple Sclerosis Exposed to Disease-Modifying Drugs (2014) (12)
Reproductive counselling for multiple sclerosis patients. (1985) (12)
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients (2016) (11)
No effect of APOE and PVRL2 on the clinical outcome of multiple sclerosis (2007) (11)
Labor induction and augmentation in women with multiple sclerosis (2013) (11)
Underlying causes of death in Down syndrome: accuracy of British Columbia death certificate data. (1990) (11)
Sex ratio in offspring of patients with multiple sclerosis. (1982) (11)
No Effect of Parental Age on Risk of Multiple Sclerosis: A Population-Based Study (2009) (11)
A goodness-of-fit test for the polygenic threshold model: application to multiple sclerosis. (1981) (11)
A Novel PS1 Gene Mutation in a Large Aboriginal Kindred (2010) (11)
Clustering of autoimmune disease in families at high risk for multiple sclerosis? (2007) (11)
TCR beta polymorphisms and multiple sclerosis. (2004) (10)
The Differential Diagnosis of Adult Onset Metachromatic Leukodystrophy and Early Onset Familial Alzheimer Disease in an Alzheimer Clinic Population (1993) (10)
The genetics of multiple sclerosis (2002) (10)
Maternal - offspring HLA-DRB1 compatibility in multiple sclerosis. (2005) (9)
Revisiting the T-cell receptor alpha/delta locus and possible associations with multiple sclerosis (2011) (9)
Use of genetic counselling services for neural tube defects. (1987) (8)
Genetics of multiple sclerosis in British Columbia and throughout Canada (1994) (8)
Incidence of neural tube defects in liveborn and stillborn infants in British Columbia over a 10-year period. (1983) (8)
MS and cognition and APOE (2008) (8)
TCR β polymorphisms and multiple sclerosis (2004) (7)
Multiple Sclerosis and Pregnancy: A Comparison Study (2013) (7)
Multiple Sclerosis and Other Demyelinating Disorders (2013) (7)
Further evidence for linkage of bipolar disorder to chromosomes 6 and 17 in a new independent pedigree series (2012) (7)
Prune belly anomaly in Down syndrome. (1987) (7)
Accuracy of Reported Family History and Effectiveness of Medical Record Requests in Genetic Counseling for Alzheimer Disease (2011) (7)
Colony stimulation factor 1 receptor (CSF1R) is not a common cause of multiple sclerosis (2013) (6)
The genetics and genetic epidemiology of multiple sclerosis: the "hard facts". (2006) (6)
Risks to sibs of probands with neural tube defects: data for clinic populations in British Columbia. (1986) (6)
Gestational diabetes and multiple sclerosis. (2009) (6)
Recurrence risk of MS in relatives of patients in flanders Belgium (1995) (6)
APOE Genotype Disclosure for Risk of Alzheimer ’ s Disease : The REVEAL Study (2009) (5)
TPP2 mutation associated with sterile brain inflammation mimicking MS (2018) (5)
Empiric recurrence risks for use in the genetic counselling of multiple sclerosis patients. (1984) (5)
Multiple Sclerosis in Northern Sardinia, Italy: A Methodological Approach for Genetic Epidemiological Studies (2003) (5)
Impact of prenatal chromosomal diagnosis in order women on population incidence of severe mental retardation. (1982) (5)
The rate of the Down syndrome among offspring of women with Alzheimer disease. (1994) (5)
CAUSES OF DEATH IN MULTIPLE-SCLEROSIS (1985) (5)
Prevalence of Extracranial venous Narrowing on Magnetic Resonance Venography is Similar in People with Multiple Sclerosis, Their Siblings, and Unrelated Healthy Controls: A Blinded, Case-Control Study (2017) (5)
The multiple sclerosis trait: a disease waiting to happen? (2004) (5)
Genetic Counselling and Genetic Screening for Alzheimer’s Disease and Other Dementias (2001) (4)
Patient-Reported Benefits of Extracranial Venous Therapy: British Columbia CCSVI Registry (2017) (4)
Venoplasty of chronic cerebral spinal venous insufficiency to improve MS patient reported outcomes is not superior to sham treatment at week 2 or week 12 (2017) (4)
Suppressor Alleles in Multiple Sclerosis: Inheritance and Interactions (2005) (4)
An Assessment of Genetic Counseling Services for Individuals with Multiple Sclerosis (2015) (4)
Survival in liveborn infants with anencephaly. (1987) (4)
Maternal age in Down syndrome. (1988) (4)
Risk factors for peripartum depression in women with multiple sclerosis (2021) (4)
Analysis of Canadian multiple sclerosis patients does not support a role for FKBP6 in disease (2018) (4)
Maternal age-specific costs of detecting Down syndrome and neural tube defects. (1982) (4)
Multiple sclerosis in Canada (1987) (3)
Genetic analysis of nucleotide-binding leucine-rich repeat (NLR) receptors in multiple sclerosis (2020) (3)
Genes and environment in multiple sclerosis: Impact of temporal changes in the sex ratio on recurrence risks (2021) (3)
Birth order, infection in early life, and multiple sclerosis – Authors' reply (2005) (3)
Early life child exposure and the risk of multiple sclerosis: A population based study (2011) (3)
Multiple sclerosis in First Nations Canadians: A pilot comparison study (2016) (3)
Canadian Multiple Sclerosis Pregnancy Study (CANPREG-MS): Rationale and Methodology (2019) (3)
To treat or not to treat the person with clinical multiple sclerosis – a dilemma (2001) (3)
Genetic counseling for early onset familial Alzheimer's disease in a large aboriginal kindred from a remote community in northern British Columbia: Unique challenges and possible solutions (2009) (3)
Demyelinating Disorders of the Central Nervous System in Childhood: Genetics of pediatric multiple sclerosis (2011) (2)
Genetic susceptibility to multiple sclerosis (1995) (2)
Sibling risks for multiple sclerosis (1996) (2)
HUNTINGTON'S DISEASE: A DISORDER OF FAMILIES. By Susan E. Folstein. Published by The John Hopkins University Press. $46 Cdn approx. (1990) (2)
A genome-scan in a single pedigree with a high prevalence of MS (2007) (2)
Update on management and genetics of multiple sclerosis. (1997) (2)
Editorial Note to:Nuclear Receptor NR1H3 in Familial Multiple Sclerosis (2016) (2)
Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families (2009) (2)
Insignificant risk for arthrogryposis multiplex congenita. (1985) (2)
A linkage study of bipolar disorder (1994) (2)
Genetics and epidemiology of multiple sclerosis. (2015) (2)
Parental non-inherited HLA resistance alleles do not confer protection against multiple sclerosis (2008) (2)
Autors' reply (2)
Analysis of NOD-like receptor NLRP1 in multiple sclerosis families (2017) (2)
Predictors of chronic cerebrospinal venous insufficiency procedure use among older people with multiple sclerosis: a national case–control study (2015) (2)
The familial nature of MS. (1983) (1)
Reanalysis of the NIMH collaborative bipolar family data: Results of complex segregation analysis (1994) (1)
Genetic factors that protect against dementia. (1994) (1)
Occurrence of neural tube defects among first-degree relatives of probands in British Columbia. (1984) (1)
Progressive multiple sclerosis does not associate with rs996343 and rs2046748 (2014) (1)
TPP 2 mutation associated with sterile brain in fl ammation mimicking MS (1)
Incidence of pyloric stenosis in British Columbia over a 12 year period. (1984) (1)
Multiple sclerosis occurrence in relatives of Sardinian multiple sclerosis patients (2001) (1)
Genetic and epidemiologic aspects of multiple sclerosis in British Columbia (1979) (1)
Mother–child blood group incompatibility and the risk of multiple sclerosis (2010) (1)
Analysis of galanin receptor GALR2 in multiple sclerosis (2019) (1)
Peripartum disease activity in moderately and severely disabled women with multiple sclerosis (2022) (1)
Basic and clinical epidemiology of MS (1995) (1)
Fetal mortality in sibships of cases with neural tube defects (1986) (1)
Possible loci for bipolar disorder on chromosome 5 near the dopamine transporter locus and on chromosome 22 (1996) (1)
The Canadian collaborative study on genetic susceptibility to multiple sclerosis: A population-based half-sib study (1995) (1)
The incidence of Down's syndrome over a 19-year period. (1984) (1)
Common genetic etiology between “multiple sclerosis-like” single-gene disorders and familial multiple sclerosis (2017) (1)
MS MORTALITY - REPLY (1992) (1)
Forty multiplex families with MS: Linkage analysis of chromosome 6 and HLA-DRB1 (2002) (0)
HLA-DRB 1 * 15 , Low Infant Sibling Exposure , and Multiple Sclerosis Gene – Environment Interaction (2010) (0)
Vitamin-D Receptor and 1-alpha-hydroxylase Genes in Risk and Outcome of Multiple Sclerosis in Canadians (2010) (0)
Contents Vol. 22, 2003 (2003) (0)
P1-283 Ethnic differences in MRI scans among Alzheimer’s disease patients and unaffected siblings in the MIRAGE Study (2006) (0)
Contents Vol. 32, 2009 (2009) (0)
A glossary of terms frequently used in epidemiology and genetics (1994) (0)
Multiple sclerosis: research in British Columbia. (1982) (0)
Variants in the promoter region of CYP7A1 are associated with neuromyelitis optica but not with multiple sclerosis in the Han Chinese population (2013) (0)
Subject Index Vol. 32, 2009 (2009) (0)
IS THERE A MATERNAL EFFECT IN MULTIPLE-SCLEROSIS (1995) (0)
Pregnancy and Multiple Sclerosis-Reply (1995) (0)
HHRR Association Results for the Dense Set of 211SNPs in Finnish and Canadian MS Families (2006) (0)
Collaborative epidemiology: From concept to execution (2008) (0)
Genetic Considerations and Reproductive Planning in Women with MS (2017) (0)
Why do relatives develop multiple sclerosis (1997) (0)
Demographic characterization and risk factors for Alzheimer's disease in patients from the UBC clinic for Alzheimer disease and related disorders (2009) (0)
Response to „anencephaly, other congenital malformations, and stillbirths”︁ (1986) (0)
Familial risk of multiple sclerosis in Northern Sardinians (2005) (0)
Reply (2001) (0)
Confirmation of linkage between the HLA-DR locus and multiple sclerosis in two unusually large MS families. (1999) (0)
Accuracy of reported family history and effectiveness of medical record requests in genetic counseling for Alzheimer's disease (2009) (0)
The Genetic Epidemiology and Epidemiology of Multiple Sclerosis: How a Registry Can Provide Invaluable Data (2011) (0)
Multiple sclerosis in Canada. Reply (1987) (0)
Co-variates influencing sib risks in multiple sclerosis: Implications for genetic counselling. (1997) (0)
A genome-wide scan for regions shared identical by descent in Hutterite MS families (2002) (0)
Kindreds for the APP (2006) (0)
P3-165 MRI traits are heritable among Alzheimer disease cases and their siblings in the MIRAGE Study (2006) (0)
Genetic analysis of nucleotide-binding leucine-rich repeat (NLR) receptors in multiple sclerosis (2020) (0)
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility (2022) (0)
CCR5 does not influence genetic susceptibility to multiple sclerosis in the Canadian population. (1999) (0)
GENETICS AND NEUROLOGY. By Bundey Sarah. Published by Churchill Livingstone, 1985. 340 pages. $70.00 Cdn. (1986) (0)
Brain morphology predicts long-term placebo response in multiple sclerosis patients (2019) (0)
Subject Index Vol. 22, 2003 (2003) (0)
P3-261: Genetic counseling issues involving a novel PS1 gene change in a large first nations kindred from a remote community in Northern British Columbia (2008) (0)
SNP Haplotypes and the Corresponding p-Values (Haploview) Tested in Finnish MS Families (2006) (0)
Reporter gene analysis of DRB1 promoter VDRE. (2013) (0)
Cortical morphology predicts placebo response in multiple sclerosis (2019) (0)
A Familial Risk Of Multiple Sclerosis In Sardinians (2007) (0)
Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progression (2014) (0)
Fine Mapping of Epigenetic Modifications in Multiple Sclerosis Susceptibility (2009) (0)
MS mortality (1992) (0)
An Extended Statistical Approach Provides Insights into Genetic Risk Factors for Multiple Sclerosis in the HLA-DRB1 Gene (2009) (0)
A novel PS1 mutation in a large aboriginal kindred with early onset familial Alzheimer's disease from a remote community in northern British Columbia (2009) (0)
Stage I: SNP Results of the Association Analysis in the Primary Study (2006) (0)
The Rate of Multiple Sclerosis (MS) In Relatives of MS Patients In The Province Of Sassari, Sardinia (2001) (0)

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