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style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'><o:p>&nbsp;</o:p></span></b></p> <p class=MsoNormal align=center style='text-align:center'><b><span style='font-size:26.0pt;font-family:"Arial","sans-serif";color:#365F91; mso-themecolor:accent1;mso-themeshade:191'><a href="lab.html"><span style='mso-ansi-font-size:26.0pt;mso-bidi-font-size:26.0pt;mso-ascii-font-family: Arial;mso-hansi-font-family:Arial'>Projects &amp; Laboratory</span></a></span></b><span class=MsoHyperlink><span style='font-size:26.0pt;font-family:"Arial","sans-serif"; mso-bidi-font-family:"Times New Roman"'><o:p></o:p></span></span></p> <p class=MsoNormal align=center style='text-align:center'><span class=MsoHyperlink><span style='font-size:26.0pt;font-family:"Arial","sans-serif"'><a href="lab.html"><span style='mso-ansi-font-size:26.0pt;mso-bidi-font-size: 26.0pt;mso-ascii-font-family:Arial;mso-hansi-font-family:Arial'>Web site</span></a></span></span><span style='color:#365F91;mso-themecolor:accent1;mso-themeshade:191'><o:p></o:p></span></p> <p class=MsoNormal><b style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'><o:p>&nbsp;</o:p></span></b></p> <p class=MsoNormal><b style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'><o:p>&nbsp;</o:p></span></b></p> <p class=MsoNormal><b style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'>B.S.</span></b><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'> in Biological Chemistry from the University of Qatar, 1994 <br> <b style='mso-bidi-font-weight:normal'>M.Sc.</b> in Molecular Biology from the Royal Institute of Technology, Stockholm, Sweden 1996<o:p></o:p></span></p> <p class=MsoNormal><b style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'>Ph.D.</span></b><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'> in Biotechnology/Biochemistry from the Royal <st1:PlaceType w:st="on">Institute</st1:PlaceType> of <st1:PlaceName w:st="on">Technology</st1:PlaceName>, <st1:place w:st="on"><st1:City w:st="on">Stockholm</st1:City></st1:place>, Sweden 2000<o:p></o:p></span></p> <p class=MsoNormal><b style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'>Postdoc</span></b><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'>: Harvard University, Boston, MA 2000-2004<o:p></o:p></span></p> <p class=MsoNormal><span style='font-size:10.0pt;font-family:"Arial","sans-serif"; color:#666666'><span style='mso-spacerun:yes'>               </span>Boston University, Boston, MA 2004-2005<o:p></o:p></span></p> <p class=MsoNormal><b style='mso-bidi-font-weight:normal'><span style='font-size:10.0pt;font-family:"Arial","sans-serif";color:#666666'>Fellow Ship</span></b><span style='font-size:10.0pt;font-family:"Arial","sans-serif"; color:#666666'>: Katz Fellow<o:p></o:p></span></p> <p class=MsoNormal><span style='font-size:10.0pt;font-family:"Arial","sans-serif"; color:#666666'><o:p>&nbsp;</o:p></span></p> <p class=MsoNormal><span style='font-family:"Verdana","sans-serif"; color:#666666'><o:p>&nbsp;</o:p></span></p> <p class=MsoNormal><span style='font-family:"Verdana","sans-serif"; color:#666666'><o:p>&nbsp;</o:p></span></p> <p class=MsoNormal><span style='font-family:"Verdana","sans-serif"; color:#666666'><o:p>&nbsp;</o:p></span></p> <p class=MsoNormal><span style='font-family:"Verdana","sans-serif"; color:#666666'>Cummings Life Science Center<br> 920 E. 58th St., Room 515<br> <st1:place w:st="on"><st1:City w:st="on">Chicago</st1:City>, <st1:State w:st="on">IL</st1:State> <st1:PostalCode w:st="on">60637</st1:PostalCode></st1:place><o:p></o:p></span></p> <p class=MsoNormal><span style='font-family:"Verdana","sans-serif"; color:#666666'>Phone: (773)834-3177 <br> Fax:<span style='mso-spacerun:yes'>     </span>(773)834-0505</span><span style='font-family:"Arial","sans-serif";color:#666666'><br> Email: samer@uchicago.edu</span><span style='font-size:7.5pt;font-family: "Arial","sans-serif";color:#666666'><br style='mso-special-character:line-break'> <![if !supportLineBreakNewLine]><br style='mso-special-character:line-break'> <![endif]></span><span style='font-size:10.5pt;font-family:"Verdana","sans-serif"; color:#666666'><o:p></o:p></span></p> </td> </tr> <tr style='mso-yfti-irow:3;mso-row-margin-left:.76%'> <td style='mso-cell-special:placeholder;border:none;padding:0in 0in 0in 0in' width="0%"><p class='MsoNormal'>&nbsp;</td> <td colspan=2 valign=top style='padding:7.5pt 7.5pt 7.5pt 7.5pt'> <p class=MsoNormal align=center style='text-align:center'><span style='font-size:10.5pt;font-family:"Verdana","sans-serif";color:#666666'><o:p>&nbsp;</o:p></span></p> <div class=MsoNormal align=center style='text-align:center'><span style='font-size:10.5pt;font-family:"Verdana","sans-serif";color:#666666'> <hr size=2 width="100%" align=center> </span></div> <p class=MsoBodyText style='text-align:justify'><o:p>&nbsp;</o:p></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>After joining the Biotechnology Department at the Royal Institute of Technology (KTH) in Stockholm, Sweden in 1994, Dr. Karamohamed studied various DNA polymerases kinetics and their kinetics. He then used his study to develop methods to further understand kinetics of various enzymes to implement in the new DNA sequencing technology that he was working on. He found that various DNA polymerases could be used as a toll for mutation detection. That provided the ability to develop and optimize a simple method for detection of various mutations. Also, his method is a real-time approach, which provided a fast and very sensitive technique to sequence single base pairs. There is no other available assay that can detect nucleotide incorporation in real-time or to the same sensitivity. He also found that by adding a washing step after each nucleotide addition he could sequence more than one base pair. That novel idea was the first work for the last 20 years to detect more than one base pair incorporation and offered real time detection that has not been described before for DNA sequencing application.<span style='mso-spacerun:yes'>  </span>all these important findings have been published in leading scientific journals and were presented at major international conferences, including the 1995 Human Genome Variation in Europe: DNA Markers, Barcelona, Spain, The 1996 Human Genome Meeting, Heidelberg, Germany, and the 9<sup>th</sup> International Bioluminescence and Chemoluminosence, Woods Hole, MA. <o:p></o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'><o:p>&nbsp;</o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>Dr. Karamohamed has been working on the development of assays for the detection and quantification of several enzymes such as NDP kinase, ATP sulfurylase, and Apyrase, which are used in Pyrosequencing. These assays have been used to characterize these enzymes in different systems, which is another major contribution Dr. Karamohamed made in recent years.<span style='mso-spacerun:yes'>  </span>The main problem in assay development is the use of modified and radio labeled material as well as the time consuming procedures, which do not give any insight on the kinetics of the reaction during the experiment.<span style='mso-spacerun:yes'>  </span>Real time detection of enzyme activity is very important for biologist to understand the right mechanism in which enzymes use their substrates and provide a fast and sensitive method that can be used for kinetics, detection and quantification in and from various biological samples.<span style='mso-spacerun:yes'>  </span>Small quantity of enzyme is usually a limitation in any test from a limited sample.<span style='mso-spacerun:yes'>  </span>However, is very difficult to locate them with current clinical tests.<o:p></o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'><o:p>&nbsp;</o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>Dr. Karamohamed developed several novel methods using Firefly Luciferase to detect very small amounts of enzymes in a very small volume experiment. His data convincingly demonstrated that these assays are very sensitive, specific, and reliable for the detection and quantification of these enzymes from biological and laboratory samples. His excellent research was selected as an entry in the Young Investigator Award at the 9<sup>th</sup> and 10<sup>th</sup> International Bioluminescence and Chemoluminosence, MA 1996 and in Italy in 1998, and was published in the Journal of Analytical Biochemistry and BioTechniques.<o:p></o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'><o:p>&nbsp;</o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>Dr. Karamohamed has also conducted extensive molecular biologic research regarding the mechanism of drug resistance of HIV-1. His findings show that nucleotides based drugs such as AZT may play an important role in drug resistance, which may lead to treatment failure. He also found that AZT is incorporated into the reaction by HIV-1 RT. These studies extend our understanding of the function of AZT as drug and nucleotide based drug resistance, and are very helpful in the development of new drugs. His work was presented at the 9<sup>th</sup> International Bioluminescence and Chemoluminosence, MA and in Italy, and was published in the journals Analytical Biochemistry and BioTechniques.<o:p></o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'><o:p>&nbsp;</o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>Dr. Karamohamed for the first time expressed the yeast ATP sulfurylase enzyme in E.coli bacteria. ATP Sulfurylase is a toxic enzyme for organisms other than yeast.<span style='mso-spacerun:yes'>  </span>However, Dr. Karamohamed used and created a whole new system to control the expression of the enzyme in bacteria.<span style='mso-spacerun:yes'>  </span>The system used cell-to-cell signal and an initiator for the expression of the enzyme. When the cell reaches high density, the signal and the protein will express in larger numbers of cells. Then, the cells will be harvested before toxicity of the ATP sulfurylase kills the bacteria cells. By this breakthrough system, the enzymes been successfully expressed and in a very large quantity. This breakthrough work opens up the possibility to further understand the kinetics of the enzyme and to characterize its properties. Dr. Karamohamed also used every available system and optimized it them, which allowed him to purify them to homogeneity and then to determine the exact molecular weight and to shape the enzyme. The work has been published in the Protein Expression and Purification journal.<o:p></o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'><o:p>&nbsp;</o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>Dr. Karamohamed is currently using his expertise in mutation detection and assay development to investigating Human Genome Variation and molecular markers. His research interest recently is focused on finding genes and markers that are associated with various human diseases including diabetes and Parkinson disease. Dr. Karamohamed is using cutting-edge molecular biologic technique like Pyrosequencing, RT-PCR and IHC<o:p></o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'><o:p>&nbsp;</o:p></span></p> <p class=MsoBodyText style='text-align:justify'><span style='font-size:10.0pt'>Part of Dr. Karamohamed s work was presented at the 52<sup>nd</sup> Annual Meeting of the American Society of Human Genetics, Baltimore, and the 14<sup>th</sup> International Genome Sequencing and Analysis Conference, Boston. Recently, he submitted an AADR (American Association of Diabetes Research) grant proposal to study the role of Insulin Degrading Enzyme (IDE) mechanisms in diabetes.</span></p> <p><em><span style='font-size:7.0pt;font-family:"Verdana","sans-serif"; color:#666666'><o:p>&nbsp;</o:p></span></em></p> <p align=center style='text-align:center'><em><span style='font-size:14.0pt; font-family:"Verdana","sans-serif"'>Current Research Focus<o:p></o:p></span></em></p> <p><em><span style='font-size:8.0pt;font-family:"Verdana","sans-serif"'>Our research focuses on the characterization and identification of heritable mutations that affect the nervous system. Research projects vary from genetic mapping of rare (Mendelian) disease mutations and characterization of their downstream consequences to the study of common heritable disorders using genomic and bioinformatic approaches. </span></em><i><span style='font-size: 8.0pt;font-family:"Verdana","sans-serif"'><br> <br> </span></i><span style='font-size:8.0pt;font-family:"Verdana","sans-serif"'>With new opportunities in genome science and bioinformatics, research has shifted toward the study of common heritable disorders including Parkinson s disease, Diabetes, COPD, autism, bipolar disorder, anxiety disorders, schizophrenia, and Alzheimer s disease. We use mouse models and disease-related  endophenotypes to inform the search for human disease genes. In the study of human anxiety disorders, we target an adaptive fear-related behavior - fear conditioning  that can be studied in humans and other model organisms. &nbsp;We collaborate in these studies with Dr. Abraham Palmer (Human Genetics). &nbsp;Similarly, in our study of schizophrenia we focus on bio-behavioral markers like working memory and executive functioning skills.&nbsp; Our group and others have shown that heritable genetic variation in genes that alter dopamine metabolism at the synaptic nerve terminals affect performance on the specific cognitive tasks that are compromised in schizophrenia patients. In the study of autism, we have used gender and language-based endophenotypes as biomarkers to reduce the genetic complexity of the target phenotype. By focusing on genetically tractable disease sub-phenotypes, we hope to gain insight into the genetic architecture of complex human diseases. <br> <br> Another approach we are pursuing is to shift the focus of gene mapping from individual gene mutations to the prediction of multi-gene patterns of inheritance. Genetic susceptibility to complex disorders arises from the fateful combination of heritable mutations distributed among multiple genes. Identification of these multigenic patterns of inheritance has proven elusive because the vast number of gene combinations that could lead to disease so dramatically exceeds the number of experimental observations possible in human studies. Assuming our genomes consist of ~ 25,000 genes, the number of possible combinations of 2, 3, and 10 genes increases exponentially from 10<sup>9</sup> to 10<sup>12</sup> to 10<sup>30</sup> respectively, in comparison to 10<sup>3</sup> to 10<sup>4</sup> observable  meiotic events in the largest human genetic studies. Thus, the  curse of dimensionality has thwarted progress in the study of common heritable disorders.</span><span style='font-size:8.0pt'><o:p></o:p></span></p> <p class=MsoNormal style='text-align:justify'><span style='font-size:8.0pt; font-family:"Verdana","sans-serif"'>We are collaborating with experts in data-mining and network topology, systems biology, large-scale computing, and statistical genetics to develop new approaches to map the multi-gene determinants of common neuropsychiatric disorders. Our current approach uses technology developed by Rzhetsky and coworkers (Medicine and Human Genetics, beginning mid-2007) to first, extract molecular interaction networks from the electronic literature, and second, combine interaction data and genetic linkage data in a common probabilistic framework that allows us to survey disease-related inheritance across groups of interacting genes. By reducing possible gene-gene combinations to those documented in the literature or whole genome databases, we avoid the penalties of multiple-testing. We are collaborating to evaluate and benchmark the new approach, to develop models for the detection of gene-gene interactions, and ultimately, to use the new approach to identify multigenic patterns of inheritance that predict an individual s susceptibility to major neuropsychiatric disorders.</span><span style='letter-spacing:-.3pt;layout-grid-mode:line;mso-bidi-font-weight:bold'><o:p></o:p></span></p> </td> </tr> <tr style='mso-yfti-irow:4;mso-yfti-lastrow:yes;mso-row-margin-left:.76%'> <td style='mso-cell-special:placeholder;border:none;padding:0in 0in 0in 0in' width="0%"><p class='MsoNormal'>&nbsp;</td> <td colspan=2 style='padding:7.5pt 7.5pt 7.5pt 7.5pt'> <div style='border:none;border-top:solid #BCBFB7 1.0pt;padding:9.0pt 0in 0in 0in' id=copyright> <p align=center style='text-align:center;line-height:150%'><span style='font-size:9.5pt;line-height:150%;font-family:"Verdana","sans-serif"; color:#333333'><a href="http://www.genes.uchicago.edu"><b><span style='font-size:10.5pt;line-height:150%'>Department of Human Genetics, University of Chicago</span></b></a><br> 920 E. 58th Street, CLSC 5th floor, &nbsp;Chicago, IL 60637<br> phone 773.834.0525 fax 773.834.0505 <o:p></o:p></span></p> </div> </td> </tr> <![if !supportMisalignedColumns]> <tr height=0> <td width=5 style='border:none'></td> <td width=310 style='border:none'></td> <td width=403 style='border:none'></td> </tr> <![endif]> </table> <p class=MsoNormal style='background:white'><o:p>&nbsp;</o:p></p> </div> </div> </body> <!-- InstanceEnd --> </html>