Fatema J Serajee, M.D.
Pediatrician and Pediatric Neurologist, Children's Hospital of Michigan
Published Articles:
Original Observations in Referred Journals
1.
Huq AHMM, Chugani DC, Hukku B, Serajee FJ. 2002. Evidence of Somatic Mosaicism
in Sturge – Weber Syndrome. Neurology 59:780-781
2.
Nabi R, Zhong H, Serajee FJ and Huq AHMM. 2003. No association between single
nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism. Am J
Med Genet; 119B:98-101
3.
Zhong H, Serajee FJ, Nabi R and Huq AHMM. 2003. No association between the EN2
gene and autistic disorder. J Med Genet 40: e4
4.
Serajee FJ, Zhong H, Nabi R and Huq AHMM. 2003. The metabotropic glutamate
receptor 8 gene at 7q31: partial duplication and possible association with autism. J Med
Genet; 40: e42 Page 1
5.
Serajee FJ, Nabi R, Zhong H and Huq AHMM. 2003. Association of INPP1, PIK3CG
and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol
signalling in autism. J Med Genet, 40: e119
6.
Serajee FJ, Nabi R, Zhong H and Huq AHMM 2004. Polymorphisms in xenobiotic
metabolism genes
and autism. J Child Neurol 19:413 - 7
7.
Nabi R, Serajee FJ, Chugani DC, Zhong H and Huq AHMM. 2004. Association of
tryptophan 2,3
dioxygenase gene polymorphism with autism. Am J Med Genet, 125B (1):63-8
8.
Serajee FJ, Zhong H and Mahbubul Huq AH 2004. Association of Reelin gene
polymorphisms in
autism. Genomics, 2006;87(1):75-83.
9.
Cerghet M, Tapos D, Serajee FJ, and Huq AHM M (2008). Homozygous myotonic
dystrophy with
craniosynostosis. J Child Neurol; 23:930-3.
10.
Serajee FJ, and Huq AHM M (2009).
Association of Y chromosome haplotypes with autism. J child
Neurology, J Child Neurol. 24:1258-61.
11.Serajee FJ, Sarnaik SA, Altinock D and Huq AHM M.
Stroke in sickle cell disease J Pediatric Neurology
(in press)
ABSTRACTS
1.
AHM Mahbubul Huq, Hailang Zhong, Rafiqun Nabi, Diane C Chugani, Fatema J
Serajee. Evidence
for an additional susceptibility region for autism on human chromosome 7q36. 31st
Annual
Meeting of the Child Neurology Society in October 9-12, 2002. Ann Neurol 2002;
52(3):S116.
2.
Fatema J Serajee, Kipp Chillag, Michael A Nigro, AHM Mahbubul Huq. Novel mutation
in MPZ (P0)
gene associated with Dejerine-Sottas and congenital hypomyelination phenotypes in the
same
family. 31st Annual Meeting of the Child Neurology Society in October 9-12, 2002. Ann
Neurol
2002; 52(3):S152.
3.
Kevin Valentine, Fatema J Serajee, Kipp Chillag, June Ventimiglia, Michael A Nigro,
AHM Mahbubul
Huq. Biochemical markers and efficacy of the ketogenic diet treatment of refractory
pediatric
epilepsy. 31st Annual Meeting of the Child Neurology Society in October 9-12, 2002.
Ann Neurol
2002; 52(3): S140.
4.
Jiang Y, Fatema J Serajee, Harry T Chugani, and AHM Mahbubul Huq.
Mitochondrial respiratory chain enzyme complex deficiencies: report of five unique
cases. 31st
Annual Meeting of the Child Neurology Society in October 9-12, 2002. Ann Neurol
2002;
52(3):S149.
5.
Fatema J Serajee, Kipp Chillag, AHM Mahbubul Huq. Early onset olivopontocerebellar
atrophies
and hypoplasia: report of five unique cases. 31st Annual Meeting of the Child Neurology
Society in
October 9-12, 2002. Ann Neurol 2002; 52(3):S150.
6.
AHM Mahbubul Huq, Diane C. Chugani, Fatema J Serajee. Somatic Mosaicism in Sturge
-Weber
Syndrome. 31st Annual Meeting of the Child Neurology Society in October 9-12, 2002.
Ann Neurol 2002; 52(3):S123.
7.
AHM Mahbubul Huq, Hailang Zhong, Rafiqun Nabi, Diane C Chugani, Fatema J
Serajee. Serotonergic neurotransmission and autism: A genetic analysis. 31st Annual
Meeting of the Child Neurology Society in October 9-12, 2002. Ann Neurol 2002;
52(3):S115.
Page 2
8.
Fatema J Serajee, Michael Mally, Diane C. Chugani and AHM Mahbubul Huq. Somatic
Mosaicism in
Sturge -Weber Syndrome. 52nd Annual Meeting of the American Society of Human
Genetics,
October 15-19, 2002
9.
AHM Mahbubul Huq, Hailang Zhong, Rafiqun Nabi and Fatema J Serajee. Analysis of
six candidate
genes for autism on 7q. 52nd Annual Meeting of the American Society of Human
Genetics, October
15-19, 2002
10.Rafiqun Nabi, Hailang Zhong, Diane C Chugani, Fatema J Serajee and AHM
Mahbubul Huq. Analysis
of five serotonin system genes in autism by association and linkage. 52nd Annual
Meeting of the
American Society of Human Genetics, October 15-19, 2002
11.Hailang Zhong, Fatema J Serajee, Rafiqun Nabi, and AHM Mahbubul Huq.
Association of the
metabotropic glutamate receptor 8 gene at 7q31 with quantitative traits in autism. 52nd
Annual
Meeting of the American Society of Human Genetics, October 15-19, 2002
12.AHM M Huq, Fatema J Serajee, Rafiqun Nabi, William E Watson, and Hailang
Zhong.
Candidate
genes for autism on chromosome 7q. 55th Annual Meeting of the American Academy of
Neurology, March 29-April 3, 2003
13.Huq AHMM, Serajee FJ, Nabi R, Zhong H and.
Investigation of 40 positional and functional
candidate genes for Autism. 32nd Annual Meeting of Child Neurology Society, 2003;
Ann Neurol
2003; 54(7):S119]
14.Serajee FJ, Nabi R, Zhong H and Huq AHMM.
Investigation of 40 positional and functional
candidate genes for Autism. XIth World congress of Psychiatric Genetics, 2003; Am J
Med Genet
2003; 122B(1):117
15.R Nabi, F J Serajee,
H Zhong, and AHM M Huq. Association analyses of 50 candidate genes for
autism from 7q21-36 region. 33rd Annual Meeting of Child Neurology Society, 2004;
Ann Neurol
2004; 56(S8): 100.
16.F J Serajee, R Nabi, H Zhong, and AHMM Huq.
Association of Reelin Gene Polymorphisms with
Autism. 33rd Annual Meeting of Child Neurology Society, 2004; Ann Neurol 2004;
56(S8): 99.
17.F J Serajee, R Nabi, H Zhong, and AHMM Huq.
Immunogenetic studies in autism: association with
IL4R and ICAM5 genes. 33rd Annual Meeting of Child Neurology Society, 2004; Ann
Neurol 2004;
56(S8): 101.
18.R Nabi, F J Serajee, H Zhong, and AHM M Huq. Serotonin neurotransmitter system
in autism:
association with HTR4, HTR6 and TDO2 polymorphisms. 33rd Annual Meeting of Child
Neurology
Society, 2004; Ann Neurol 2004; 56(S8): 99.
19.R Nabi, F J Serajee, H Zhong, and AHM M Huq.
Genetics of phosphatidylinositol signaling in
autism. 33rd Annual Meeting of Child Neurology Society, 2004; Ann Neurol 2004;
56(S8): 103.
20.F J Serajee, R Nabi, H Zhong, and AHM M Huq.
Association of chromosome 15 GABA-A receptor
subunit genes with autism. 33rd Annual Meeting of Child Neurology Society, 2004; Ann
Neurol
2004; 56(S8): 103.
21.R Nabi, F J Serajee1, H Zhong, and AHM M Huq.
Distribution and heritability of phenotypic traits in
autism. 33rd Annual Meeting of Child Neurology Society, 2004; Ann Neurol 2004;
56(S8): 105.
22.R Nabi, F J Serajee, H Zhong, and AHM M Huq.
Association analyses of EN2 gene in autism. 34th
Annual Meeting of Child Neurology Society, 2005; Ann Neurol 2005; 58(S9): 108.
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23.F J Serajee, R Nabi, H Zhong, and AHM M Huq.
Association of mitochondrial aspartate/glutamate
carrier SLC25A12 and SLC25A13 genes with autism. 34th Annual Meeting of Child
Neurology
Society, 2005; Ann Neurol 2005; 58(S9): 105.
24.F J Serajee, R Nabi, H Zhong, and AHM M Huq.
Association of Y chromosome haplotypes with
autism. 34th Annual Meeting of Child Neurology Society, 2005; Ann Neurol 2005;
58(S9): 82.
25.Fatema. J. Serajee, Hailang Zhong, AHM M Huq.
Prevalence of common mitochondrial point
mutations in autism. Platform presentation at the 10th International Child Neurology
Congress,
June 11-16, 2006, Montreal, Canada, Abstract 577
26.Fatema. J. Serajee, Hailang Zhong, AHM M Huq.
Immunogenetic studies in autism. Platform
presentation at the 10th International Child Neurology Congress, June 11-16, 2006,
Montreal,
Canada, Abstract A693
27.Fatema. J. Serajee, Hailang Zhong, AHM M Huq.
Y Chromosome Effect in Autism. 60th Annual
Meeting of the American Academy of Neurology, April 12 -April 19, 2008 (recipient of
travel
research award)
28. Fatema. J. Serajee, Hailang Zhong, AHM M Huq.
Mitochondrial haplogroups in Autism. 60th
Annual Meeting of the American Academy of Neurology, April 12 -April 19, 2008
29.Ridwan Alam, Fatema J. Serajee, AHM M Huq.
Dose Response to Oxcarbazepine in Children with
Newly Diagnosed Partial Epilepsy. 61st Annual Meeting of the American Academy of
Neurology,
April 25 – May 02, 2009
30.Huq Naznin Mahmood, Farhan Murshed, Fatema J. Serajee, AHM M Huq.
Ketogenic Diet Treatment
of Intractable Epilepsy. 61st Annual Meeting of the American Academy of Neurology,
April 25 –
May 02, 2009
31.Fatema J. Serajee, AHM M Huq. Genetic Association Studies of Immune Genes in
Autism (recipient
of travel research award). 61st Annual Meeting of the American Academy of Neurology,
April 25 –
May 02, 2009
32.Fatema J. Serajee, AHM M Huq. Metabolite testing in developmental delay. Abstract
# 27, 38th
annual meeting of Child Neurology Society, October 14-17, 2009; Annals of Neurology
66 (suppl
13): S106, 2009
33.Fatema J. Serajee, Huq F, Wu Y, AHM M Huq. A mitochondrial polymorphism
reduces the risk of
autism. Abstract 28, 38th annual meeting of Child Neurology Society, October 14-17,
2009;
Annals of Neurology 66 (suppl 13): S106, 2009
34.Fatema J. Serajee, Elizabeth Leleszi, AHM M Huq. Oligogenic inheritance in a
mitochondrial
disorder. Abstract *22, 38th annual meeting of Child Neurology Society, October 14-17,
2009;
Annals of Neurology 66 (suppl 13): S104, 2009
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