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Bernard Chodirker

Research Profile

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Manitoba

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Publications

TOP 3
Michael S Salman; Anindita Tjahjadi; Esther J Lee; Bernard N Chodirker
The epidemiology of intermittent and chronic ataxia in children in Manitoba, Canada.
Asnat Walfisch; Bernard N Chodirker; Kelsey E Mills; Howard Berger
Prenatal screening characteristics in Emanuel syndrome: a case series and review of the literature.
Simone S Vaz; Bernard N Chodirker; Albert E Chudley; Chitra Prasad; Jamie A Seabrook; Asuri N Prasad
Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study.

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All Publications

2013: Michael S Salman; Anindita Tjahjadi; Esther J Lee; Bernard N Chodirker
The epidemiology of intermittent and chronic ataxia in children in Manitoba, Canada.
Developmental medicine and child neurology 2013;55(4):341-7.
2012: Asnat Walfisch; Bernard N Chodirker; Kelsey E Mills; Howard Berger
Prenatal screening characteristics in Emanuel syndrome: a case series and review of the literature.
Archives of gynecology and obstetrics 2012;286(2):299-302.
2012: Simone S Vaz; Bernard N Chodirker; Albert E Chudley; Chitra Prasad; Jamie A Seabrook; Asuri N Prasad
Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study.
American journal of medical genetics. Part A 2012;158A(4):751-8.
2012: Alison M Elliott; Cheryl R Greenberg; Sandra L Marles; Aizeddin A Mhanni; Gwendolyne C Nyhof; Albert E Chudley; Bernard N Chodirker
Trends in telehealth versus on-site clinical genetics appointments in Manitoba: a comparative study.
Journal of genetic counseling 2012;21(2):337-44.
2012: Rebecca L Hood; Chong Ae Kim; Didier Lacombe; Matthew A Lines; Jacek Majewski; Janet Marcadier; George McGillivray; D Ross McLeod; Jukka S Moilanen; Sarah M Nikkel; Małgorzata J M Nowaczyk; Konrad Platzer; Caio Robledo D C Quaio; Jeremy Schwartzentruber; Susan M White; Margo L Whiteford; Dagmar Wieczorek; Ruobing Zou; Beate Albrecht; Judith Allanson; Chandree Beaulieu; Debora R Bertola; Dennis E Bulman; Bernard N Chodirker; Albert E Chudley; Gabriele Gillessen-Kaesbach; Israel Gomy; Kym M Boycott
Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome.
American journal of human genetics 2012;90(2):308-13.
2011: Mariya Kozenko; Titi Oluyomi-Obi; Daniel Sitar; Alison M Elliott; David Grynspan; Bernard N Chodirker
Potential teratogenic effects of allopurinol: a case report.
American journal of medical genetics. Part A 2011;155A(9):2247-52.
2011: Marc R Del Bigio; Albert E Chudley; Harvey B Sarnat; Craig Campbell; Sharan Goobie; Bernard N Chodirker; Duygu Selcen
Infantile muscular dystrophy in Canadian aboriginals is an αB-crystallinopathy.
Annals of neurology 2011;69(5):866-71.
2011: Bernard N Chodirker; Angelika J Dawson
Recurrent miscarriage.
The New England journal of medicine 2011;364(8):783; author reply 784.
2010: Andrew R MacRae; Bernard N Chodirker; Gregory A Davies; Glenn E Palomaki; George J Knight; Jane Minett; Peter A Kavsak; Ants Toi; David Chitayat; Paul G Van Caeseele
Second and first trimester estimation of risk for Down syndrome: implementation and performance in the SAFER study.
Prenatal diagnosis 2010;30(5):459-66.
2010: Belinda Lategan; Bernard N Chodirker; Marc R Del Bigio
Fetal hydrocephalus caused by cryptic intraventricular hemorrhage.
Brain pathology (Zurich, Switzerland) 2010;20(2):391-8.
2008: Bernard N Chodirker; Albert E Chudley
Routine genetic testing for Asperger syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(11):843-5; author reply 845.
2008: AJ Rusnak; Marie I Hadfield; Albert E Chudley; Sandra L Marles; Gregory J Reid; Bernard N Chodirker
Increased nuchal translucency thickness: a potential indicator for Ritscher-Schinzel syndrome.
Fetal diagnosis and therapy 2008;24(4):395-9.
2007: Asuri N Prasad; Kelly Bunzeluk; Chitra Prasad; Bernard N Chodirker; Kenneth G Magnus; Cheryl R Greenberg
Agenesis of the corpus callosum and cerebral anomalies in inborn errors of metabolism.
Congenital anomalies 2007;47(4):125-35.
2007: Kym M Boycott; Jillian S Parboosingh; James N Scott; D Ross McLeod; Cheryl R Greenberg; T Mary Fujiwara; Jean K Mah; Julian Midgley; Andrew Wade; Francois P Bernier; Bernard N Chodirker; Martin Bunge; A Micheil Innes
Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome.
American journal of medical genetics. Part A 2007;143A(15):1715-25.
2007: Chumei Li; Sandra L Marles; Cheryl R Greenberg; Bernard N Chodirker; Jiddeke van de Kamp; Anne Slavotinek; Albert E Chudley
Manitoba Oculotrichoanal (MOTA) syndrome: report of eight new cases.
American journal of medical genetics. Part A 2007;143A(8):853-7.
2006: Tina Babineau; Heather L Wilson; Angelika J Dawson; Bernard N Chodirker; Vazken M Der Kaloustian; Suzanne Demczuk; Heather E McDermid
Unusual dicentric chromosome 22 associated with a 22q13 deletion.
American journal of medical genetics. Part A 2006;140(24):2819-23.
2006: Alison M Elliott; Martin H Reed; Albert E Chudley; Bernard N Chodirker; Jane A Evans
Clinical and epidemiological findings in patients with central ray deficiency: split hand foot malformation (SHFM) in Manitoba, Canada.
American journal of medical genetics. Part A 2006;140(13):1428-39.
2006: Terrence P Szajkowski; Bernard N Chodirker; Karen M MacDonald; Jane A Evans
Maternal serum alpha-fetoprotein levels in fetal hydrocephalus: a retrospective population based study.
BMC pregnancy and childbirth 2006;6():23.
2005: Kirandeep Birdi; Asuri N Prasad; Chitra Prasad; Bernard N Chodirker; Albert E Chudley
The floppy infant: retrospective analysis of clinical experience (1990-2000) in a tertiary care facility.
Journal of child neurology 2005;20(10):803-8.
2005: Natalie K Björklund; Karen M MacDonald; Jane A Evans; Carol E Schneider; Bernard N Chodirker
Screening for open neural tube defects from 21 to 25 weeks' gestation: the Manitoba experience.
Prenatal diagnosis 2005;25(8):715-7.
2005: Bernard N Chodirker; Namrata S Shah; Martin K Bunge; Martin H Reed
Another case of Varadi-Papp Syndrome with a molar tooth sign.
American journal of medical genetics. Part A 2005;136A(4):416-7.
2004: Bernard N Chodirker; Albert E Chudley
Genetic landmarks through philately--epilepsy and clinical genetic issues.
Clinical genetics 2004;66(4):290-2.
2004: Natalie K Björklund; Jane A Evans; Cheryl R Greenberg; LORNE SEARGEANT; Carol E Schneider; Bernard N Chodirker
The C677T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoprotein.
Reproductive biology and endocrinology : RB&E 2004;2():65.
2004: Chumei C Li; Bernard N Chodirker; Angelika J Dawson; Albert E Chudley
Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell-Silver syndrome?
Clinical dysmorphology 2004;13(2):95-8.
2003: R Brian Lowry; A Micheil Innes; Francois P Bernier; D Ross McLeod; Cheryl R Greenberg; Albert E Chudley; Bernard N Chodirker; Sandra L Marles; MJ Crumley; J Concepción Loredo-Osti; Kenneth Morgan; T Mary Fujiwara
Bowen-Conradi syndrome: a clinical and genetic study.
American journal of medical genetics. Part A 2003;120A(3):423-8.
2003: Albert E Chudley; Bernard N Chodirker
Landmarks in genetics through philately: Down syndrome.
Clinical genetics 2003;63(4):268-72.
2002: Angelika J Dawson; S Putnam; J Schultz; D Riordan; Chitra Prasad; Cheryl R Greenberg; Bernard N Chodirker; Aizeddin A Mhanni; Albert E Chudley
Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.
Clinical genetics 2002;62(6):488-94.
2002: Bernard N Chodirker; Sandra L Marles; Albert E Chudley
A not-so-"new" mental retardation syndrome.
American journal of medical genetics 2002;111(1):106; author reply 107-8.
2002: Ahmet A Baschat; Christopher R Harman; Gehan Farid; Bernard N Chodirker; Jane A Evans
Very low second-trimester maternal serum alpha-fetoprotein: Association with high birth weight.
Obstetrics and gynecology 2002;99(4):531-6.
2001: Bernard N Chodirker; Albert E Chudley
Monsters, myths and syndromes depicted on stamps.
Clinical genetics 2001;59(4):244-7.
2000: Jane A Evans; S Phillips; M Reed; Bernard N Chodirker
Severe acro-renal-uterine-mandibular syndrome.
American journal of medical genetics 2000;93(1):67-73.
2000: Aizeddin A Mhanni; Bernard N Chodirker; Jane A Evans; S Menticouglou; N Wiseman; N MacDonald; Albert E Chudley
Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein.
Prenatal diagnosis 2000;20(5):432-5.
2000: Chitra Prasad; Asuri N Prasad; Bernard N Chodirker; C Lee; A K Dawson; LJ Jocelyn; Albert E Chudley
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
Clinical genetics 2000;57(2):103-9.
1999: Albert E Chudley; Angelika J Dawson; Bernard N Chodirker; LJ Jocelyn
Children with PDD need to be evaluated by clinical geneticists. Pervasive developmental disorder.
Journal of developmental and behavioral pediatrics : JDBP 1999;20(1):72-3.
1998: Albert E Chudley; E Gutierrez; LJ Jocelyn; Bernard N Chodirker
Outcomes of genetic evaluation in children with pervasive developmental disorder.
Journal of developmental and behavioral pediatrics : JDBP 1998;19(5):321-5.
1998: Edmond G Lemire; Bernard N Chodirker; GJ Williams; LORNE SEARGEANT; Sara J Israels; S M Phillips; J A de Nanassy; John M Maris; Rochelle Yanofsky
Familial neuroblastoma: report of a kindred with later age at diagnosis.
Journal of pediatric hematology/oncology 1998;20(5):489-93.
1997: Bernard N Chodirker; Cheryl R Greenberg; N G Giddins; Angelika J Dawson; Jane A Evans; Albert E Chudley
Low MSAFP levels and Williams syndrome.
American journal of medical genetics 1997;72(4):448-50.
1995: Angelika J Dawson; Bernard N Chodirker; Albert E Chudley
Frequency of FMR1 premutations in a consecutive newborn population by PCR screening of Guthrie blood spots.
Biochemical and molecular medicine 1995;56(1):63-9.
1995: Y Yamashiro; Bernard N Chodirker; D Hobson; Meir H Kryger
A familial awake movement disorder mimicking restless legs in a sleep apnea patient.
Sleep 1995;18(7):604-7.
1995: S L Marles; Bernard N Chodirker; Cheryl R Greenberg; Albert E Chudley
Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.
American journal of medical genetics 1995;56(4):343-50.
1994: Bernard N Chodirker; L B Erdile; K M MacDonald; Christopher R Harman; Mary Cheang; Jane A Evans
MSAFP levels in aboriginal Canadian women.
Canadian journal of public health. Revue canadienne de santé publique 1994;85(6):424-6.
1994: Bernard N Chodirker; Albert E Chudley; K M MacDonald; Christopher R Harman; Jane A Evans
MSAFP levels and oesophageal atresia.
Prenatal diagnosis 1994;14(11):1086-9.
1994: Bernard N Chodirker; Albert E Chudley
Male-to-male transmission of mild Brachmann-de Lange syndrome.
American journal of medical genetics 1994;52(3):331-3.
1994: S M Gorski; K J Adams; P H Birch; Bernard N Chodirker; Cheryl R Greenberg; Paul J Goodfellow
Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds.
Human genetics 1994;94(2):141-8.
1994: P M Kyle; Christopher R Harman; J A Evans; K MacDonald; Savas M Menticoglou; F A Manning; Bernard N Chodirker
Life without amniocentesis: elevated maternal serum alpha-fetoprotein in the Manitoba program 1986-91.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 1994;4(3):199-204.
1994: H Albar; K M MacDonald; Christopher R Harman; Jane A Evans; Bernard N Chodirker
Elevated MSAFP levels and congenital heart defects: lack of an association.
American journal of medical genetics 1994;49(3):337-40.
1993: Cheryl R Greenberg; C L Taylor; James C Haworth; LORNE SEARGEANT; S Philipps; Barbara L Triggs-Raine; Bernard N Chodirker
A homoallelic Gly317-->Asp mutation in ALPL causes the perinatal (lethal) form of hypophosphatasia in Canadian mennonites.
Genomics 1993;17(1):215-7.
1992: Cheryl R Greenberg; H K Jacobs; T E Nylen; M Gibb; Bernard N Chodirker; M Moffatt; A Lacson; William C Halliday; F Bernier; A el-Husseini
Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophy.
Journal of medical genetics 1992;29(8):583-5.
1992: Bernard N Chodirker; Cheryl R Greenberg; P D Pabello; Albert E Chudley
Paracentric inversion 11q in Canadian Hutterites.
Human genetics 1992;89(4):450-2.
1991: Bernard N Chodirker; D Roy; Cheryl R Greenberg; Mary Cheang; J A Evans; M H Reed
Computer assisted analysis of hand radiographs in infantile hypophosphatasia carriers.
Pediatric radiology 1991;21(3):216-9.
1990: Bernard N Chodirker; R Jenkins
Mosaic isochromosome 20q found on amniocentesis with normal outcome.
Prenatal diagnosis 1990;10(7):469-72.
1990: Bernard N Chodirker; Christopher R Harman; Cheryl R Greenberg
Survival of fetuses with abnormal karyotypes and cystic hygromas detected prenatally.
Prenatal diagnosis 1990;10(2):136.
1990: Bernard N Chodirker; J A Evans; LORNE SEARGEANT; Mary Cheang; Cheryl R Greenberg
Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening.
American journal of human genetics 1990;46(2):280-5.
1990: Cheryl R Greenberg; J A Evans; S McKendry-Smith; S Redekopp; James C Haworth; R Mulivor; Bernard N Chodirker
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers.
American journal of human genetics 1990;46(2):286-92.
1990: Bernard N Chodirker; S P Coburn; LORNE SEARGEANT; M P Whyte; Cheryl R Greenberg
Increased plasma pyridoxal-5'-phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia.
Journal of inherited metabolic disease 1990;13(6):891-6.
1989: J Stephen Bamforth; C O Leonard; Bernard N Chodirker; D Chitayat; H L Gritter; J A Evans; B Keena; T Pantzar; Jan M Friedman; Judith G Hall
Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.
American journal of medical genetics 1989;32(1):93-9.
1988: Bernard N Chodirker; M Ray; P J McAlpine; D Riordan; A Vust; D Pugh; Albert E Chudley
Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.
American journal of medical genetics 1988;31(1):145-51.
1988: Bernard N Chodirker; Christopher R Harman; Cheryl R Greenberg
Spontaneous resolution of a cystic hygroma in a fetus with Turner syndrome.
Prenatal diagnosis 1988;8(4):291-6.
1987: Bernard N Chodirker; J A Evans; M Lewis; Gail Coghlan; E Belcher; S Philipps; LORNE SEARGEANT; C Sus; Cheryl R Greenberg
Infantile hypophosphatasia--linkage with the RH locus.
Genomics 1987;1(3):280-2.
1987: Bernard N Chodirker; Albert E Chudley; M H Reed; T V Persaud
Possible prenatal hydantoin effect in a child born to a nonepileptic mother.
American journal of medical genetics 1987;27(2):373-8.
1986: Bernard N Chodirker; Albert E Chudley; M A Toffler; M H Reed
Zimmerman-Laband syndrome and profound mental retardation.
American journal of medical genetics 1986;25(3):543-7.