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Items: 1 to 50 of 54

1.

Children with autism observe social interactions in an idiosyncratic manner.

Avni I, Meiri G, Bar-Sinai A, Reboh D, Manelis L, Flusser H, Michaelovski A, Menashe I, Dinstein I.

Autism Res. 2019 Oct 26. doi: 10.1002/aur.2234. [Epub ahead of print]

PMID:
31654504
2.

Language regression is associated with faster early motor development in children with autism spectrum disorder.

Manelis L, Meiri G, Ilan M, Flusser H, Michaelovski A, Faroy M, Kerub O, Dinstein I, Menashe I.

Autism Res. 2019 Aug 30. doi: 10.1002/aur.2197. [Epub ahead of print]

PMID:
31468744
3.

Risk Factors Before Dialysis Predominate as Mortality Predictors in Diabetic Maintenance Dialysis patients.

Tsur N, Menashe I, Haviv YS.

Sci Rep. 2019 Jul 23;9(1):10633. doi: 10.1038/s41598-019-46919-w.

4.

Quantifying the social symptoms of autism using motion capture.

Budman I, Meiri G, Ilan M, Faroy M, Langer A, Reboh D, Michaelovski A, Flusser H, Menashe I, Donchin O, Dinstein I.

Sci Rep. 2019 May 22;9(1):7712. doi: 10.1038/s41598-019-44180-9.

5.

Exposure to General Anesthesia May Contribute to the Association between Cesarean Delivery and Autism Spectrum Disorder.

Huberman Samuel M, Meiri G, Dinstein I, Flusser H, Michaelovski A, Bashiri A, Menashe I.

J Autism Dev Disord. 2019 Aug;49(8):3127-3135. doi: 10.1007/s10803-019-04034-9.

PMID:
31053992
6.

Autism Spectrum Disorder: Evolution of Disorder Definition, Risk Factors and Demographic Characteristics in Israel.

Kerub O, Haas E, Menashe I, Davidovitch N, Meiri G.

Isr Med Assoc J. 2018 Sep;20(9):576-581. Review. No abstract available.

7.

A Comparison Between Two Screening Approaches for ASD Among Toddlers in Israel.

Kerub O, Haas EJ, Meiri G, Davidovitch N, Menashe I.

J Autism Dev Disord. 2018 Aug 11. doi: 10.1007/s10803-018-3711-x. [Epub ahead of print]

PMID:
30099656
8.

Sleep disturbances are associated with specific sensory sensitivities in children with autism.

Tzischinsky O, Meiri G, Manelis L, Bar-Sinai A, Flusser H, Michaelovski A, Zivan O, Ilan M, Faroy M, Menashe I, Dinstein I.

Mol Autism. 2018 Mar 27;9:22. doi: 10.1186/s13229-018-0206-8. eCollection 2018.

9.

Autism Prevalence and Severity in Bedouin-Arab and Jewish Communities in Southern Israel.

Levaot Y, Meiri G, Dinstein I, Menashe I, Shoham-Vardi I.

Community Ment Health J. 2019 Jan;55(1):156-160. doi: 10.1007/s10597-018-0236-x. Epub 2018 Jan 31.

PMID:
29388003
10.

Characteristics Associated with Drug Prescription and Compliance Among Young Children with Autism Spectrum Disorder.

Meiri G, Azoulay H, Menashe I.

J Child Adolesc Psychopharmacol. 2018 Apr;28(3):232-237. doi: 10.1089/cap.2017.0092. Epub 2017 Dec 21.

PMID:
29266976
11.

Brief Report: The Negev Hospital-University-Based (HUB) Autism Database.

Meiri G, Dinstein I, Michaelowski A, Flusser H, Ilan M, Faroy M, Bar-Sinai A, Manelis L, Stolowicz D, Yosef LL, Davidovitch N, Golan H, Arbelle S, Menashe I.

J Autism Dev Disord. 2017 Sep;47(9):2918-2926. doi: 10.1007/s10803-017-3207-0.

PMID:
28631035
12.

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.

Larsen E, Menashe I, Ziats MN, Pereanu W, Packer A, Banerjee-Basu S.

Mol Autism. 2016 Oct 21;7:44. doi: 10.1186/s13229-016-0103-y. eCollection 2016.

13.

The Unique Evolutionary Signature of Genes Associated with Autism Spectrum Disorder.

Tsur E, Friger M, Menashe I.

Behav Genet. 2016 Nov;46(6):754-762. Epub 2016 Aug 11.

PMID:
27515661
14.

Cell-type-specific neuroanatomy of cliques of autism-related genes in the mouse brain.

Grange P, Menashe I, Hawrylycz M.

Front Comput Neurosci. 2015 May 29;9:55. doi: 10.3389/fncom.2015.00055. eCollection 2015.

15.

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.

Mol Autism. 2013 Oct 3;4(1):36. doi: 10.1186/2040-2392-4-36.

16.

Co-expression profiling of autism genes in the mouse brain.

Menashe I, Grange P, Larsen EC, Banerjee-Basu S, Mitra PP.

PLoS Comput Biol. 2013;9(7):e1003128. doi: 10.1371/journal.pcbi.1003128. Epub 2013 Jul 25.

17.

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database.

Menashe I, Larsen EC, Banerjee-Basu S.

PLoS One. 2013 Jun 18;8(6):e66707. doi: 10.1371/journal.pone.0066707. Print 2013.

18.

Polymorphisms in pattern-recognition genes in the innate immunity system and risk of non-Hodgkin lymphoma.

Hu W, Bassig BA, Xu J, Zheng T, Zhang Y, Berndt SI, Holford TR, Hosgood HD 3rd, Leaderer B, Yeager M, Menashe I, Boyle P, Zou K, Zhu Y, Chanock S, Lan Q, Rothman N.

Environ Mol Mutagen. 2013 Jan;54(1):72-7. doi: 10.1002/em.21739. Epub 2012 Oct 11.

19.

Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background.

Menashe I, Figueroa JD, Garcia-Closas M, Chatterjee N, Malats N, Picornell A, Maeder D, Yang Q, Prokunina-Olsson L, Wang Z, Real FX, Jacobs KB, Baris D, Thun M, Albanes D, Purdue MP, Kogevinas M, Hutchinson A, Fu YP, Tang W, Burdette L, Tardón A, Serra C, Carrato A, García-Closas R, Lloreta J, Johnson A, Schwenn M, Schned A, Andriole G Jr, Black A, Jacobs EJ, Diver RW, Gapstur SM, Weinstein SJ, Virtamo J, Caporaso NE, Landi MT, Fraumeni JF Jr, Chanock SJ, Silverman DT, Rothman N.

PLoS One. 2012;7(1):e29396. doi: 10.1371/journal.pone.0029396. Epub 2012 Jan 4.

20.

A brain region-specific predictive gene map for autism derived by profiling a reference gene set.

Kumar A, Swanwick CC, Johnson N, Menashe I, Basu SN, Bales ME, Banerjee-Basu S.

PLoS One. 2011;6(12):e28431. doi: 10.1371/journal.pone.0028431. Epub 2011 Dec 9.

21.

Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma.

Bassig BA, Zheng T, Zhang Y, Berndt SI, Holford TR, Hosgood HD 3rd, Hu W, Leaderer B, Yeager M, Menashe I, Boyle P, Xu J, Zou K, Zhu Y, Chanock S, Rothman N, Lan Q.

Environ Mol Mutagen. 2012 Mar;53(2):145-51. doi: 10.1002/em.21675. Epub 2011 Dec 15.

22.

Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead.

van Bemmel DM, Boffetta P, Liao LM, Berndt SI, Menashe I, Yeager M, Chanock S, Karami S, Zaridze D, Matteev V, Janout V, Kollarova H, Bencko V, Navratilova M, Szeszenia-Dabrowska N, Mates D, Slamova A, Rothman N, Han SS, Rosenberg PS, Brennan P, Chow WH, Moore LE.

PLoS One. 2011;6(7):e20432. doi: 10.1371/journal.pone.0020432. Epub 2011 Jul 20.

23.

The association between inflammation-related genes and serum androgen levels in men: the prostate, lung, colorectal, and ovarian study.

Meyer TE, Chu LW, Li Q, Yu K, Rosenberg PS, Menashe I, Chokkalingam AP, Quraishi SM, Huang WY, Weiss JM, Kaaks R, Hayes RB, Chanock SJ, Hsing AW.

Prostate. 2012 Jan;72(1):65-71. doi: 10.1002/pros.21407. Epub 2011 Apr 25.

24.

Genetic variation in Th1/Th2 pathway genes and risk of non-Hodgkin lymphoma: a pooled analysis of three population-based case-control studies.

Lan Q, Wang SS, Menashe I, Armstrong B, Zhang Y, Hartge P, Purdue MP, Holford TR, Morton LM, Kricker A, Cerhan JR, Grulich A, Cozen W, Zahm SH, Yeager M, Vajdic CM, Schenk M, Leaderer B, Yuenger J, Severson RK, Chatterjee N, Chanock SJ, Zheng T, Rothman N.

Br J Haematol. 2011 May;153(3):341-50. doi: 10.1111/j.1365-2141.2010.08424.x. Epub 2011 Mar 21.

25.

A case-control study reveals immunoregulatory gene haplotypes that influence inhibitor risk in severe haemophilia A.

Lozier JN, Rosenberg PS, Goedert JJ, Menashe I.

Haemophilia. 2011 Jul;17(4):641-9. doi: 10.1111/j.1365-2516.2010.02473.x. Epub 2011 Mar 1.

26.

A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non-Hodgkin lymphoma risk.

Hosgood HD 3rd, Purdue MP, Wang SS, Zheng T, Morton LM, Lan Q, Menashe I, Zhang Y, Cerhan JR, Grulich A, Cozen W, Yeager M, Holford TR, Vajdic CM, Davis S, Leaderer B, Kricker A, Schenk M, Zahm SH, Chatterjee N, Chanock SJ, Rothman N, Hartge P, Armstrong B.

Br J Haematol. 2011 Mar;152(6):721-6. doi: 10.1111/j.1365-2141.2010.08518.x. Epub 2011 Jan 20.

27.

Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma.

Wang SS, Menashe I, Cerhan JR, Cozen W, Severson RK, Davis S, Hutchinson A, Rothman N, Chanock SJ, Bernstein L, Hartge P, Morton LM.

Cancer Epidemiol Biomarkers Prev. 2011 Jan;20(1):42-9. doi: 10.1158/1055-9965.EPI-10-0638. Epub 2010 Dec 10.

28.

Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma in a pooled analysis of three studies.

Shen M, Menashe I, Morton LM, Zhang Y, Armstrong B, Wang SS, Lan Q, Hartge P, Purdue MP, Cerhan JR, Grulich A, Cozen W, Yeager M, Holford TR, Vajdic CM, Davis S, Leaderer B, Kricker A, Severson RK, Zahm SH, Chatterjee N, Rothman N, Chanock SJ, Zheng T.

Br J Haematol. 2010 Nov;151(3):239-44. doi: 10.1111/j.1365-2141.2010.08364.x. Epub 2010 Aug 31.

29.

Variation in innate immunity genes and risk of multiple myeloma.

Purdue MP, Lan Q, Menashe I, Zheng T, Zhang Y, Yeager M, Hosgood HD 3rd, Zahm SH, Chanock SJ, Rothman N, Baris D.

Hematol Oncol. 2011 Mar;29(1):42-6. doi: 10.1002/hon.954.

30.

Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut.

Lee KM, Baris D, Zhang Y, Hosgood HD 3rd, Menashe I, Yeager M, Zahm SH, Wang SS, Purdue MP, Chanock S, Zheng T, Rothman N, Lan Q.

Am J Hematol. 2010 Aug;85(8):560-3. doi: 10.1002/ajh.21760.

31.

Association between genetic variants in the 8q24 cancer risk regions and circulating levels of androgens and sex hormone-binding globulin.

Chu LW, Meyer TE, Li Q, Menashe I, Yu K, Rosenberg PS, Huang WY, Quraishi SM, Kaaks R, Weiss JM, Hayes RB, Chanock SJ, Hsing AW.

Cancer Epidemiol Biomarkers Prev. 2010 Jul;19(7):1848-54. doi: 10.1158/1055-9965.EPI-10-0101. Epub 2010 Jun 15.

32.

Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade.

Menashe I, Maeder D, Garcia-Closas M, Figueroa JD, Bhattacharjee S, Rotunno M, Kraft P, Hunter DJ, Chanock SJ, Rosenberg PS, Chatterjee N.

Cancer Res. 2010 Jun 1;70(11):4453-9. doi: 10.1158/0008-5472.CAN-09-4502. Epub 2010 May 11.

33.

Re: Racial disparities in cancer survival among randomized clinical trials of the Southwest Oncology Group.

Rosenberg PS, Menashe I, Jatoi I, Anderson WF.

J Natl Cancer Inst. 2010 Feb 24;102(4):277; author reply 280-2. doi: 10.1093/jnci/djp510. Epub 2010 Jan 14. No abstract available.

34.

Variants in blood pressure genes and the risk of renal cell carcinoma.

Andreotti G, Boffetta P, Rosenberg PS, Berndt SI, Karami S, Menashe I, Yeager M, Chanock SJ, Zaridze D, Matteev V, Janout V, Kollarova H, Bencko V, Navratilova M, Szeszenia-Dabrowska N, Mates D, Rothman N, Brennan P, Chow WH, Moore LE.

Carcinogenesis. 2010 Apr;31(4):614-20. doi: 10.1093/carcin/bgp321. Epub 2010 Jan 4.

35.

Genetic determinants of serum lipid levels in Chinese subjects: a population-based study in Shanghai, China.

Andreotti G, Menashe I, Chen J, Chang SC, Rashid A, Gao YT, Han TQ, Sakoda LC, Chanock S, Rosenberg PS, Hsing AW.

Eur J Epidemiol. 2009;24(12):763-74. doi: 10.1007/s10654-009-9402-3. Epub 2009 Nov 4.

36.

Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk.

Moore LE, Brennan P, Karami S, Menashe I, Berndt SI, Dong LM, Meisner A, Yeager M, Chanock S, Colt J, Schwartz K, Davis F, Zaridze D, Mattveev V, Janout V, Kollarova H, Bencko V, Navratilova M, Szeszenia-Dabrowska N, Mates D, Holcatova I, Boffetta P, Chow WH, Rosenberg PS, Rothman N.

Cancer Res. 2009 Oct 15;69(20):8001-8. doi: 10.1158/0008-5472.CAN-09-1734. Epub 2009 Oct 6.

37.

Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk.

Karami S, Brennan P, Rosenberg PS, Navratilova M, Mates D, Zaridze D, Janout V, Kollarova H, Bencko V, Matveev V, Szeszenia-Dabrowska N, Holcatova I, Yeager M, Chanock S, Menashe I, Rothman N, Chow WH, Boffetta P, Moore LE.

PLoS One. 2009 Sep 15;4(9):e7013. doi: 10.1371/journal.pone.0007013.

38.

PTEN identified as important risk factor of chronic obstructive pulmonary disease.

Hosgood HD 3rd, Menashe I, He X, Chanock S, Lan Q.

Respir Med. 2009 Dec;103(12):1866-70. doi: 10.1016/j.rmed.2009.06.016. Epub 2009 Jul 21.

39.

An analysis of growth, differentiation and apoptosis genes with risk of renal cancer.

Dong LM, Brennan P, Karami S, Hung RJ, Menashe I, Berndt SI, Yeager M, Chanock S, Zaridze D, Matveev V, Janout V, Kollarova H, Bencko V, Schwartz K, Davis F, Navratilova M, Szeszenia-Dabrowska N, Mates D, Colt JS, Holcatova I, Boffetta P, Rothman N, Chow WH, Rosenberg PS, Moore LE.

PLoS One. 2009 Mar 24;4(3):e4895. doi: 10.1371/journal.pone.0004895.

40.

Underlying causes of the black-white racial disparity in breast cancer mortality: a population-based analysis.

Menashe I, Anderson WF, Jatoi I, Rosenberg PS.

J Natl Cancer Inst. 2009 Jul 15;101(14):993-1000. doi: 10.1093/jnci/djp176. Epub 2009 Jul 7.

41.

Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies.

Lan Q, Morton LM, Armstrong B, Hartge P, Menashe I, Zheng T, Purdue MP, Cerhan JR, Zhang Y, Grulich A, Cozen W, Yeager M, Holford TR, Vajdic CM, Davis S, Leaderer B, Kricker A, Schenk M, Zahm SH, Chatterjee N, Chanock SJ, Rothman N, Wang SS.

Blood. 2009 Jul 9;114(2):264-7. doi: 10.1182/blood-2009-01-198697. Epub 2009 May 4.

42.

Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk.

Wang SS, Purdue MP, Cerhan JR, Zheng T, Menashe I, Armstrong BK, Lan Q, Hartge P, Kricker A, Zhang Y, Morton LM, Vajdic CM, Holford TR, Severson RK, Grulich A, Leaderer BP, Davis S, Cozen W, Yeager M, Chanock SJ, Chatterjee N, Rothman N.

PLoS One. 2009;4(4):e5360. doi: 10.1371/journal.pone.0005360. Epub 2009 Apr 24.

43.

Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk.

Hosgood HD 3rd, Baris D, Zhang Y, Berndt SI, Menashe I, Morton LM, Lee KM, Yeager M, Zahm SH, Chanock S, Zheng T, Lan Q.

Leuk Res. 2009 Dec;33(12):1609-14. doi: 10.1016/j.leukres.2009.03.013. Epub 2009 Apr 11.

44.

Risk of non-Hodgkin lymphoma associated with germline variation in genes that regulate the cell cycle, apoptosis, and lymphocyte development.

Morton LM, Purdue MP, Zheng T, Wang SS, Armstrong B, Zhang Y, Menashe I, Chatterjee N, Davis S, Lan Q, Vajdic CM, Severson RK, Holford TR, Kricker A, Cerhan JR, Leaderer B, Grulich A, Yeager M, Cozen W, Hoar Zahm S, Chanock SJ, Rothman N, Hartge P.

Cancer Epidemiol Biomarkers Prev. 2009 Apr;18(4):1259-70. doi: 10.1158/1055-9965.EPI-08-1037. Epub 2009 Mar 31.

45.

Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China.

Shen M, Vermeulen R, Rajaraman P, Menashe I, He X, Chapman RS, Yeager M, Thomas G, Burdett L, Hutchinson A, Yuenger J, Chanock S, Lan Q.

Environ Mol Mutagen. 2009 May;50(4):285-90. doi: 10.1002/em.20452.

46.

Age-related crossover in breast cancer incidence rates between black and white ethnic groups.

Anderson WF, Rosenberg PS, Menashe I, Mitani A, Pfeiffer RM.

J Natl Cancer Inst. 2008 Dec 17;100(24):1804-14. doi: 10.1093/jnci/djn411. Epub 2008 Dec 9.

47.

A pooled investigation of Toll-like receptor gene variants and risk of non-Hodgkin lymphoma.

Purdue MP, Lan Q, Wang SS, Kricker A, Menashe I, Zheng TZ, Hartge P, Grulich AE, Zhang Y, Morton LM, Vajdic CM, Holford TR, Severson RK, Leaderer BP, Cerhan JR, Yeager M, Cozen W, Jacobs K, Davis S, Rothman N, Chanock SJ, Chatterjee N, Armstrong BK.

Carcinogenesis. 2009 Feb;30(2):275-81. doi: 10.1093/carcin/bgn262. Epub 2008 Nov 24.

48.

Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway.

Hosgood HD 3rd, Menashe I, Shen M, Yeager M, Yuenger J, Rajaraman P, He X, Chatterjee N, Caporaso NE, Zhu Y, Chanock SJ, Zheng T, Lan Q.

Carcinogenesis. 2008 Oct;29(10):1938-43. doi: 10.1093/carcin/bgn178. Epub 2008 Aug 1.

49.

PGA: power calculator for case-control genetic association analyses.

Menashe I, Rosenberg PS, Chen BE.

BMC Genet. 2008 May 13;9:36. doi: 10.1186/1471-2156-9-36.

50.

Genetic elucidation of human hyperosmia to isovaleric acid.

Menashe I, Abaffy T, Hasin Y, Goshen S, Yahalom V, Luetje CW, Lancet D.

PLoS Biol. 2007 Oct 30;5(11):e284.

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