700 Childrens Dr
Columbus, OH 43205
Phone: (614) 722-3545
Assistant Professor-Clinical, Pediatrics
Volunteer with BuddyUp Tennis- organization that teaches tennis skills to children and adults with Down syndrome (2011-current); appointed to board of directors for organization (March 2013)
I am a faculty coach for 8 students in the College of Medicine class of 2016. This entails reviewing their performance over a block, planning ahead for their careers and general support.
I am also a Med-Peds mentor for a 2nd year resident.
|2011 - present||The Ohio State University.|
|2012 - present||The Ohio State University.|
|2012 - present||Anita Narayanan Nationwide Children's Hospital and The Ohio State University. Autism in Down Syndrome|
|2007 - present||Fellow of American Board of Internal Medicine: American Board of Internal Medicine|
|2009 - present||Fellow of the American Board of Medical Genetics: American Board of Medical Genetics|
|2011||Comparative Effectiveness Research training: The Ohio State University|
|2002||M.D., Royal College of Surgeons in Ireland|
|present||American Board of Medical Genetics|
|present||American Board of Genetic Counselors|
|2013 - present||Familial Cancer|
|2002||Dan Kelly Memorial Award. Royal College of Surgeons in Ireland.|
|2007 - present||NIH training grant for Masters of Public Health. National Institute of Health/University of North Carolina at Chapel Hill.|
|2007 - 2008||Visting Scholar-Externship. NHGRI.|
|2011 - 2012||Scholarship for Comparative Effectiveness Research Training Program. OSU CCTS and School of Public Health.|
|2012||Best Doctors in Columbus. Columbus Monthly.|
|2013 - present||Citizenship Award. Nationwide Childrens.|
|2014||Down syndrome association of Central Ohio honoree. Down Syndrome Association of Central Ohio.|
Adams SA, Coppinger J, Saitta SC, Stroud T, Kandamurugu M, Fan Z, Ballif BC, Shaffer LG, Bejjani BA.. "Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH." Genetics in Medicine. Vol. 5, no. 11. (January 2009.): 314-322.
Cottrell,Catherine,E; Prior,Thomas,W; Pyatt,Robert; Astbury,Caroline; Reshmi,Shalini; Bartholomew,Dennis; Atkin,Joan; Manickam,Kandamurugu; Thrush,Devon,Lamb; Pastore,Matthew; Mendell,Jerry; Tsao,Chang-Yong; Al-Dahhak,Roula; Newmeyer,Amy; Gastier-Foster,Julie,M. "Unexpected Detection of Dystrophin Gene Deletions by Array Comparative Genomic Hybridization." AMERICAN JOURNAL OF MEDICAL GENETICS PART A. Vol. 152A, no. 9. (September 2010.): 2301-2307.
McBride,Kim,L; Varga,Elizabeth,A; Pastore,Matthew,T; Prior,Thomas,W; Manickam,Kandamurugu; Atkin,Joan,F; Herman,Gail,E. "Confirmation Study of PTEN Mutations Among Individuals with Autism or Developmental Delays/Mental Retardation and Macrocephaly." AUTISM RESEARCH. Vol. 3, no. 3. (June 2010.): 137-141.
Facio,Flavia,M; Feero,W,Gregory; Linn,Amy; Oden,Neal; Manickam,Kandamurugu; Biesecker,Leslie,G. "Validation of My Family Health Portrait for six common heritable conditions." GENETICS IN MEDICINE. Vol. 12, no. 6. (June 2010.): 370-375.
Morton,Sara,Anne (Adams); Coppinger,Justine; Ballif,Blake,C; Shaffer,Lisa,G; Ellison,Jay,W; Saitta,Sulagna,C; Stroud,Tracy; Manickam,Kandamurugu; Fan,Zheng. "Regarding cancer predisposition detected by CHG arrays Response." GENETICS IN MEDICINE. Vol. 13, no. 11. (November 2011.): 982-983.
Kitzmiller,Joseph,P; Embi,Peter,J; Manickam,Kandamurugu; Sweet,Kevin,M; Phelps,Mitch,A; Jackson,Rebecca,D; Marsh,Clay,B; Sadee,Wolfgang. "Program in Pharmacogenomics at the Ohio State University Medical Center." PHARMACOGENOMICS. Vol. 13, no. 7. (May 2012.): 751-756.
Sturm,Amy,C; Manickam,Kandamurugu. "Direct-to-Consumer Personal Genomic Testing: A Case Study and Practical Recommendations for "Genomic Counseling"." JOURNAL OF GENETIC COUNSELING. Vol. 21, no. 3. (June 2012.): 402-412.
Manickam,K; Allain,D; Grover,M. "Physical health and well-being of adults with Down syndrome." JOURNAL OF INTELLECTUAL DISABILITY RESEARCH. Vol. 56, no. 7-8. (July 2012.): 760-760.
Rosenfeld JA; Amrom D; Andermann E; Andermann F; Veilleux M; Curry C; Fisher J; Deputy S; Aylsworth AS; Powell CM; Manickam K; Heese B; Maisenbacher M; Stevens C; Ellison JW; Upton S; Moeschler J; Torres-Martinez W; Stevens A; Marion R; Pereira EM; Babcock M; Morrow B; Sahoo T; Lamb AN; Ballif BC; Paciorkowski AR; Shaffer LG. "Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.." Neurogenetics. Vol. 13, no. 1. (February 2012.): 31-.
Shuldiner,A,R; RELLING,M,V; Peterson,J,F; Hicks,J,K; Freimuth,R,R; Sadee,W; Pereira,N,L; Roden,D,M; Johnson,J,A; Klein,T,E. "The Pharmacogenomics Research Network Translational Pharmacogenetics Program: Overcoming Challenges of Real-World Implementation." CLINICAL PHARMACOLOGY & THERAPEUTICS. Vol. 94, no. 2. (August 2013.): 207-210.
Sturm,Amy,Curry; Sweet,Kevin; Manickam,Kandamurugu. "Implementation of a clinical research pharmacogenomics program at an academic medical center: role of the genetics healthcare professional." PHARMACOGENOMICS. Vol. 14, no. 7. (May 2013.): 703-706.
Manickam,Kandamurugu; Donoghue,Daniel,J; Meyer,April,N; Snyder,Pamela,J; Prior,Thomas,W. "Suppression of severe achondroplasia with developmental delay and acanthosis nigricans by the p.Thr651Pro mutation.." American journal of medical genetics. Part A. Vol. 164, no. 1. (January 2014.): 243-250.
Mullegama,Sureni,V; Rosenfeld,Jill,A; Orellana,Carmen; van Bon,Bregje,WM; Halbach,Sara; Repnikova,Elena,A; Brick,Lauren; Li,Chumei; Dupuis,Lucie; Rosello,Monica; Aradhya,Swaroop; Stavropoulos,D,James; Manickam,Kandamurugu; Mitchell,Elyse; Hodge,Jennelle,C; Talkowski,Michael,E; Gusella,James,F; Keller,Kory; Zonana,Jonathan; Schwartz,Stuart; Pyatt,Robert,E; Waggoner,Darrel,J; Shaffer,Lisa,G; Lin,Angela,E; de Vries,Bert,BA; Mendoza-Londono,Roberto; Elsea,Sarah,H. "Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.." European journal of human genetics. Vol. 22, no. 1. (January 2014.): 57-63.
Sweet K, Gordon ES, Sturm AC, Schmidlen TJ, Manickam K, et al.. "Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease." Journal of Personalized Medicine. Vol. 1, (January 2014.): 1-19.
|January 2008||Kandamurugu Manickam."Chondrodysplasia Punctata and maternal mixed connective disease." .|
|July 2013||Kandamurugu Manickam."Guidance on Genetic Testing for Younger Sibling of Child with Autism" Autism Speaks|
|Kandamurugu Manickam."Genomics 101"|
|Kandamurugu Manickam."Genetics of diabetes"|
|Kandamurugu Manickam."Genetics of Alzheimers disease"|
"More than we bargained for." Presented at American Society of Bioethics and Humanities, Cleveland, OH. (January 2008)
"Impact of the Genetic Information Non-Discrimination Act." Presented at Huntington Disease Society of North Carolina, Raleigh, NC, US|USA. (January 2008)
"Chondrodysplasia Punctata and maternal mixed connective disease." Presented at American College of Medical Genetics annual meeting, Phoenix, AZ, US|USA. (January 2008)
"Prenatal diagnosis of Cornelia de Lange." Presented at American College of Medical Genetics meeting, Tampa Bay, FL, US|USA. (January 2009)
"Personalized Medicine at Ohio State." Presented at Leadership retreat for OSU Medical Center, Columbus, OH, US|USA. (January 2009)
"Introduction to P4 Medicine." Presented at Introduction to P4 Medicine (P4 interest group), . (November 2011)
"P4 Scholars Program." Presented at OSU Medical Center Leadership Retreat (April 2011), Columbus, OH, US|USA. (January 2011)
"P4 Medicine: introduction." Presented at Royal College of Surgeons in Ireland Alumni Meeting, Dublin, IE|IRL. (September 2012)
"P4 Scholars Program." Presented at P4 Medicine Conference at the Ohio State University, Columbus, OH, US|USA. (October 2012)
"OSUWMC AMB Genomic Clinics/Genomics Panel." Presented at EPIC User Group Meeting, Verona, WI, US|USA. (September 2013)
|present||Johns Hopkins University Applied Physics Laboratory (JHU/APL) and the Uniformed Services University. Department of Defense. Washington DC, DC.|
|2010 - present||CDC GAPPNet Family History Working Group. Center for Disease Contol GAPPNet.|
|2011 - present||Pharmacogenomics Research Network. Pharmacogenomics Research Network (PGRN).|
|2012 - present||National Genomic Centers. National Health Genetics Research Institute.|
|2012 - present||Board of Directors. Down Syndrome Association of Central Ohio. Columbus, OH.|
|2013 - present||NHGRI Genomic Centers. NHGRI. Dallas, TX.|
|2013 - present||EPIC Genomics Working Group. EPIC electronic medical record.|