SyedMJalalMD

PubMed

• 46 citations
  Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: A retrospective analysis of 5555 samples attempted by conventional cy...
  Brandon M. Shearer, Erik C. Thorland, Austin W. Carlson, Syed M. Jalal, Rhett P. Ketterling> ;Genetics in Medicine. 2011 Jun 1
• Chromosomal mechanisms of aminoglycoside resistance in Pseudomonas aeruginosa isolates from cystic fibrosis patients.
  Islam S, Oh H, Jalal S, Karpati F, Ciofu O, Høiby N, Wretlind B> ;Clin. Microbiol. Infect.. 2009-01-01
• 19 citations
  Tetrasomy 9p: an emerging syndrome.
  Syed M. Jalal, Mary K. Kukolich, Mary Garcia, Toni R. Benjamin, Donald W. Day> ;Clinical Genetics. 2008 Jun 28
• 3 citations
  Maternal cell contamination of buccal smear samples in nursing neonates.
  Dusica Babovic-Vuksanovic, Virginia V. Michels, Mark E. Law, Noralane M. Lindor, Syed M. Jalal> ;Clinical Genetics. 2008 Jun 28
• 53 citations
  Rothmund‐Thomson syndrome in siblings: evidence for acquired in vivo mosaicism
  Noralane M. Lindor, Ellen M. G. Devries, Virginia V. Michels, Christopher R. Schad, Syed M. Jalal, Kathleen M. Donovan, William A. Smithson, Larry K. Kvols, Stephen N....> ;Clinical Genetics. 2008 Jun 28
• 27 citations
  Mosaic trisomy 16 in a thriving infant; maternal heterodisomy for chromosome 16
  Noralane M. Lindor, Syeed M. Jalal, Stephen N. Thibodeau, Denise Bonde, Kristen L. Sauser, Pamela S. Karnes> ;Clinical Genetics. 2008 Apr 23
• Ready reference to common segmental aneusomies by syndromic names, major features and chromosomal locations.
  Elyse Mitchell, Kimberly Leonhard, Peggy J Stupca, Syed M. Jalal, Noralane M. Lindor> ;Journal of the Association of Genetic Technologists. 2008 Jan 1
• 5 citations
  Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic events.
  Malini Sathanoori, Jie Hu, V. Murthy, A. Byrnes, Jerry Vockley, R. Safier, J. Bedoyan, Syed M. Jalal, H. Huber, Urvashi Surti> ;American Journal of Medical Genetics. Part A. 2007 May 1
• 21 citations
  Delineation of the cryptic 1qter deletion phenotype.
  J. Lawrence Merritt, Ying Zou, Syed M. Jalal, Virginia V. Michels> ;American Journal of Medical Genetics. Part A. 2007 Mar 15
• 26 citations
  Severe suppression of Frzb/sFRP3 transcription in osteogenic sarcoma
  Deendayal Mandal, Alok Srivastava, Eric W. Mahlum, Dinakar Desai, Avudaiappan Maran, Michael J. Yaszemski, Syed M. Jalal, Steven Gitelis, Franco Bertoni, Tim Damron, R...> ;Gene. 2007 Jan 15
• 74 citations
  6q deletion in Waldenström macroglobulinemia is associated with features of adverse prognosis.
  Enrique M. Ocio, Roelandt F.J. Schop, B. Gonzalez, S Van Wier, J.M. Hernández-Rivas, Norma C. Gutiérrez, R. García-Sanz, Moro Mj, C. Aguilera, J M Hernández, Ruifang X...> ;British Journal of Haematology. 2007 Jan 1
• 3 citations
  Multiple primary tumors associated with chromosome 9p deletion.
  Noralane M. Lindor, Syed M. Jalal, Seema Kumar, Aida N. Lteif> ;American Journal of Medical Genetics. Part A. 2007 Jan 1
• 37 citations
  Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review
  Ying S. Zou, Daniel L. Van Dyke, Erik C. Thorland, Harinderpal S. Chhabra, Virginia V. Michels, Jeannette G. Keefe, Melanie A. Lega, Molly A. Feely, Timothy S. Uphoff,...> ;American Journal of Medical Genetics. Part A. 2006 Aug 1
• 95 citations
  Prognostic factors for hyperdiploid-myeloma: effects of chromosome 13 deletions and IgH translocations
  Wee Joo Chng, Rafael Santana-Davila, S Van Wier, Gregory J. Ahmann, Syed M. Jalal, P L Bergsagel, Marta Chesi, M. C. Trendle, Susanna Jacobus, Emily A. Blood, Martin M...> ;Leukemia. 2006 May 1
• 20 citations
  Ploidy status rarely changes in myeloma patients at disease progression
  Wee Joo Chng, Jerry M. Winkler, P R Greipp, Syed M. Jalal, P L Bergsagel, Marta Chesi, M. C. Trendle, Gregory J. Ahmann, Kim Henderson, Emily A. Blood, Martin M. Oken,...> ;Leukemia Research. 2006 Mar 1
• 13 citations
  Familial Adenomatous Polyposis and Mental Retardation Caused by a de novo Chromosomal Deletion at 5q15-q22: Report of a Case
  Robert Finch, Harvey G. Moore, Noralane M. Lindor, Syed M. Jalal, Arnold J. Markowitz, Suresh C. Jhanwar, Kenneth Offit, Jose G. Guillem> ;Diseases of the Colon and Rectum. 2005 Oct 3
• 83 citations
  A validated FISH trisomy index demonstrates the hyperdiploid and nonhyperdiploid dichotomy in MGUS
  Wee Joo Chng, Scott Van Wier, Gregory J. Ahmann, Jerry M. Winkler, Syed M. Jalal, Peter Leif Bergsagel, Marta Chesi, M. C. Trendle, Martin M. Oken, Emily A. Blood, Kim...> ;Blood. 2005 Sep 15
• 32 citations
  Subtelomere deletions and translocations are frequently familial.
  Adewale Adeyinka, S. Annie Adams, Cindy Pham Lorentz, Daniel L. Van Dyke, Syed M. Jalal> ;American Journal of Medical Genetics. Part A. 2005 May 15
• 11 citations
  Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies.
  Regina Ensenauer, William J. Shaughnessy, Syed M. Jalal, D. Brian Dawson, Laura K. Courteau, Jay W. Ellison> ;American Journal of Medical Genetics. Part A. 2005 Apr 15
• 141 citations
  Position effects due to chromosome breakpoints that map ∼900 Kb upstream and ∼1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia
  Gopalrao V.N. Velagaleti, Gabriel A. Bien-Willner, Jill K. Northup, Lillian H. Lockhart, Judy C. Hawkins, Syed M. Jalal, Marjorie Withers, James R. Lupski, Pawel Stank...> ;American Journal of Human Genetics. 2005 Apr 1
• 52 citations
  Molecular diagnosis of Ewing's sarcoma/primitive neuroectodermal tumor in formalin-fixed paraffin-embedded tissues by RT-PCR and fluorescence in situ hybridization.
  Xiang Qian, Long Jin, Brandon M. Shearer, Rhett P. Ketterling, Syed M. Jalal, Ricardo V. Lloyd> ;Diagnostic Molecular Pathology. 2005 Mar 1
• 8 citations
  14q32.3 deletion syndrome with autism.
  J. Lawrence Merritt, Syed M. Jalal, William J. Barbaresi, Dusica Babovic-Vuksanovic> ;American Journal of Medical Genetics. Part A. 2005 Feb 15
• 62 citations
  Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies
  Luc M. Beauchesne, Carole A. Warnes, Heidi M. Connolly, Naser M. Ammash, Martha Grogan, Syed M. Jalal, Virginia V. Michels> ;Journal of the American College of Cardiology. 2005 Feb 15
• 109 citations
  Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb
  Adewale Adeyinka, Kimberly J. Stockero, Heather C. Flynn, Cindy Pham Lorentz, Rhett P. Ketterling, Syed M. Jalal> ;Genetics in Medicine. 2004 Nov 1
• Expression of the MexXY efflux pump in amikacin-resistant isolates of Pseudomonas aeruginosa.
  Islam S, Jalal S, Wretlind B> ;Clin. Microbiol. Infect.. 2004-10-01
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