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Chantelle Wolpert

Research Profile

Disorders

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Publications

TOP 3
Chantelle M Wolpert; Marcy C Speer
Harnessing the power of the pedigree.
Chantelle M Wolpert; Margaret L Singer; Marcy C Speer
Speaking the language of genetics: a primer.
Yulia A Dementieva; Danica D Vance; Shannon L Donnelly; Leigh A Elston; Chantelle M Wolpert; Sarah A Ravan; G Robert DeLong; Ruth K Abramson; Harry H Wright; Michael Cuccaro
Accelerated head growth in early development of individuals with autism.

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All Publications

2005: Chantelle M Wolpert; Marcy C Speer
Harnessing the power of the pedigree.
Journal of midwifery & women's health 2005;50(3):189-96.
2005: Chantelle M Wolpert; Margaret L Singer; Marcy C Speer
Speaking the language of genetics: a primer.
Journal of midwifery & women's health 2005;50(3):184-8.
2005: Yulia A Dementieva; Danica D Vance; Shannon L Donnelly; Leigh A Elston; Chantelle M Wolpert; Sarah A Ravan; G Robert DeLong; Ruth K Abramson; Harry H Wright; Michael Cuccaro
Accelerated head growth in early development of individuals with autism.
Pediatric neurology 2005;32(2):102-8.
2005: Ruth K Abramson; Sarah A Ravan; Harry H Wright; Kristin M Wieduwilt; Chantelle M Wolpert; S A Donnelly; Margaret Pericak-Vance; Michael Cuccaro
The relationship between restrictive and repetitive behaviors in individuals with autism and obsessive compulsive symptoms in parents.
Child psychiatry and human development 2005;36(2):155-65.
2005: Chantelle M Wolpert; Margaret C Schmidt
Genetic testing: understanding basics.
JAAPA : official journal of the American Academy of Physician Assistants 2005;18(1):48-52.
2005: Chantelle M Wolpert
Surgeon General launches new public health campaign: the family history initiative.
JAAPA : official journal of the American Academy of Physician Assistants 2005;18(1):20-2.
2003: Regina M Carney; Chantelle M Wolpert; Sarah A Ravan; Mona Shahbazian; Allison Ashley-Koch; Michael Cuccaro; Jeffery Vance; Margaret Pericak-Vance
Identification of MeCP2 mutations in a series of females with autistic disorder.
Pediatric neurology 2003;28(3):205-11.
2003: Yujun Shao; Michael Cuccaro; Elizabeth R Hauser; Kimberly L Raiford; Marisa M Menold; Chantelle M Wolpert; Sarah A Ravan; L Elston; K Decena; Shannon L Donnelly; Ruth K Abramson; Harry H Wright; G Robert DeLong; John Gilbert; Margaret Pericak-Vance
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
American journal of human genetics 2003;72(3):539-48.
2003: Michael Cuccaro; Yujun Shao; Meredyth P Bass; Ruth K Abramson; Sarah A Ravan; Harry H Wright; Chantelle M Wolpert; Shannon L Donnelly; Margaret Pericak-Vance
Behavioral comparisons in autistic individuals from multiplex and singleton families.
Journal of autism and developmental disorders 2003;33(1):87-91.
2003: Michael Cuccaro; Yujan Shao; Janet Grubber; Michael Slifer; Chantelle M Wolpert; Shannon L Donnelly; Ruth K Abramson; Sarah A Ravan; Harry H Wright; G Robert DeLong; Margaret Pericak-Vance
Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R.
Child psychiatry and human development 2003;34(1):3-17.
2002: Yujun Shao; Kimberly L Raiford; Chantelle M Wolpert; Heidi A Cope; Sarah A Ravan; Allison Ashley-Koch; Ruth K Abramson; Harry H Wright; Robert G DeLong; John Gilbert; Michael Cuccaro; Margaret Pericak-Vance
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.
American journal of human genetics 2002;70(4):1058-61.
2002: Pinky A McCoy; Yujun Shao; Chantelle M Wolpert; Shannon L Donnelly; Allison Ashley-Koch; Heidi L Abel; Sarah A Ravan; Ruth K Abramson; Harry H Wright; G Robert DeLong; Michael Cuccaro; John Gilbert; Margaret Pericak-Vance
No association between the WNT2 gene and autistic disorder.
American journal of medical genetics 2002;114(1):106-9.
2002: Yujun Shao; Chantelle M Wolpert; Kimberly L Raiford; Marisa M Menold; Shannon L Donnelly; Sarah A Ravan; Meredyth P Bass; Cate McClain; Lennart von Wendt; Jeffery Vance; Ruth H Abramson; Harry H Wright; Allison Ashley-Koch; John Gilbert; Robert G DeLong; Michael Cuccaro; Margaret Pericak-Vance
Genomic screen and follow-up analysis for autistic disorder.
American journal of medical genetics 2002;114(1):99-105.
2001: Chantelle M Wolpert; Shannon L Donnelly; Michael Cuccaro; Dale Hedges; C P Poole; Harry H Wright; John Gilbert; Margaret Pericak-Vance
De novo partial duplication of chromosome 7p in a male with autistic disorder.
American journal of medical genetics 2001;105(3):222-5.
2001: Allison Ashley-Koch; E R Bonner; Perry C Gaskell; Sandra G West; RW Tim; Chantelle M Wolpert; R Jones; C D Farrell; Martha Nance; Ingrid K Svenson; Douglas A Marchuk; Rose-Mary N Boustany; Jeffery Vance; William Scott; Margaret Pericak-Vance
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Neurogenetics 2001;3(2):91-7.
2001: Marisa M Menold; Yujun Shao; Chantelle M Wolpert; Shannon L Donnelly; Kimberly L Raiford; Eden R Martin; Sarah A Ravan; Ruth K Abramson; Harry H Wright; G Robert DeLong; Michael Cuccaro; Margaret Pericak-Vance; John Gilbert
Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.
Journal of neurogenetics 2001;15(3-4):245-59.
2000: Chantelle M Wolpert; Marisa M Menold; Meredyth P Bass; Mazin B Qumsiyeh; Shannon L Donnelly; Sarah A Ravan; Jeffery Vance; John Gilbert; Ruth K Abramson; Harry H Wright; Michael Cuccaro; Margaret Pericak-Vance
Three probands with autistic disorder and isodicentric chromosome 15.
American journal of medical genetics 2000;96(3):365-72.
2000: Shannon L Donnelly; Chantelle M Wolpert; Marisa M Menold; Meredyth P Bass; John Gilbert; Michael Cuccaro; G Robert DeLong; Margaret Pericak-Vance
Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome.
American journal of medical genetics 2000;96(3):312-6.
2000: Meredyth P Bass; Marisa M Menold; Chantelle M Wolpert; Shannon L Donnelly; Sarah A Ravan; Elizabeth R Hauser; Lee Maddox; Jeffery Vance; Ruth K Abramson; Harry H Wright; John Gilbert; Michael Cuccaro; G Robert DeLong; Margaret Pericak-Vance
Genetic studies in autistic disorder and chromosome 15.
Neurogenetics 2000;2(4):219-26.
2000: Eden R Martin; Marisa M Menold; Chantelle M Wolpert; Meredyth P Bass; Shannon L Donnelly; Sarah A Ravan; Andrew W Zimmerman; John Gilbert; Jeffery Vance; Lee Maddox; Harry H Wright; Ruth K Abramson; G Robert DeLong; Michael Cuccaro; Margaret Pericak-Vance
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.
American journal of medical genetics 2000;96(1):43-8.
2000: Marcy C Speer; Timothy M George; David S Enterline; A Franklin; Chantelle M Wolpert; Thomas H Milhorat
A genetic hypothesis for Chiari I malformation with or without syringomyelia.
Neurosurgical focus 2000;8(3):E12.
1999: Allison Ashley-Koch; Chantelle M Wolpert; Marisa M Menold; L Zaeem; S Basu; Shannon L Donnelly; Sarah A Ravan; CM Powell; Mazin B Qumsiyeh; Arthur S Aylsworth; Jeffery Vance; John Gilbert; Harry H Wright; Ruth K Abramson; G Robert DeLong; Michael Cuccaro; Margaret Pericak-Vance
Genetic studies of autistic disorder and chromosome 7.
Genomics 1999;61(3):227-36.
1997: William Scott; Perry C Gaskell; F Lennon; Chantelle M Wolpert; Marisa M Menold; Arthur S Aylsworth; C Warner; C D Farrell; Rose-Mary N Boustany; S G Albright; E Boyd; H M Kingston; W J Cumming; Jeffery Vance; Margaret Pericak-Vance
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
Neurogenetics 1997;1(2):95-102.
1997: Margaret Pericak-Vance; Marcy C Speer; F Lennon; Sandra G West; Marisa M Menold; Jeffrey M Stajich; Chantelle M Wolpert; BD Slotterbeck; M Saito; RW Tim; M P Rozear; Lefkos T Middleton; S Tsuji; Jeffery Vance
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity.
Neurogenetics 1997;1(2):89-93.
1996: Jeffery Vance; Marcy C Speer; Jeffrey M Stajich; Sandra G West; Chantelle M Wolpert; Perry C Gaskell; F Lennon; R M Tim; M Rozear; K B Othmane
Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.
American journal of human genetics 1996;59(1):258-62.
1995: A Kumar; R S Kandt; Chantelle M Wolpert; Allen D Roses; Margaret Pericak-Vance; John Gilbert
Mutation analysis of the TSC2 gene in an African-American family.
Human molecular genetics 1995;4(12):2295-8.
1995: Marcy C Speer; H M Kingston; Rose-Mary N Boustany; Perry C Gaskell; L C Robinson; F Lennon; Chantelle M Wolpert; LH Yamaoka; SG Kahler; Edward Leo Hogan
Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia.
American journal of medical genetics 1995;60(4):307-11.
1995: A Kumar; Chantelle M Wolpert; R S Kandt; J Segal; J Pufky; Allen D Roses; Margaret Pericak-Vance; John Gilbert
A de novo frame-shift mutation in the tuberin gene.
Human molecular genetics 1995;4(8):1471-2.