RobertWMarionMD

PubMed

• 6 citations
  Caregiver-reported characteristics of children diagnosed with pathogenic variants in KDM5C
  Hayden A. M. Hatch, Molly H. O'Neil, Robert W. Marion, Julie Secombe, Lisa H. Shulman> ;American Journal of Medical Genetics. Part A. 2021 Jun 4
• 4 citations
  The Glycogen Storage Disorders.
  Robert W. Marion, Esma D. Paljevic> ;Pediatrics in Review. 2020 Jan 1
• Corrigendum to: An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome (Human Mutation, (2015), 36, 8, (764-773), 10.1002/humu.22805)
  Marika L. Osterbur, Renjian Zheng, Robert W. Marion, Christine A. Walsh, Thomas V. McDonald> ;Human Mutation. 2019 Mar 1
• 9 citations
  Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case series.
  Nori Williams, Robert W. Marion, Thomas V. McDonald, Dawei Wang, Bo Zhou, Lucy S. Eng, Sung Yon Um, Ying Lin, Kevin Ruiter, Lisa Rojas, Barbara A. Sampson, Yingying Tang> ;Cardiovascular Pathology. 2018 Nov 1
• Hyperlipidemia secondary to acitretin therapy for lamellar ichthyosis associated with a NIPAL4 mutation improves on a plant-based diet and relapses on a standard Weste...
  Jonathan C. Lin, Daniele Massera, M. H. Ghalib, Robert W. Marion, Lauren Graf, Steven R. Cohen, Robert J. Ostfeld> ;Clinical Nutrition ESPEN. 2018 Apr 1
• 2 citations
  Contiguous Gene Syndromes
  Elaine Pereira, Robert W. Marion> ;Pediatrics in Review. 2018 Jan 1
• 6 citations
  Perceptions of an implantable cardioverter-defibrillator: A qualitative study of families with a history of sudden life-threatening cardiac events and recommendations ...
  Jarrett Linder, Nadia Hidayatallah, Marina Stolerman, Thomas V. McDonald, Robert W. Marion, Christine A. Walsh, Siobhan M. Dolan> ;The Einstein Journal of Biology and Medicine. 2016 Mar 2
• 2 citations
  Genetic drift: a case of abuse
  Robert W. Marion> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2015 Dec 1
• 3 citations
  An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome.
  Marika L. Osterbur, Renjian Zheng, Robert W. Marion, Christine A. Walsh, Thomas V. McDonald> ;Human Mutation. 2015 Aug 1
• 29 citations
  Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?
  Rick D. Vavolizza, Isha Kalia, Kathleen Erskine Aaron, Louise Bordeaux Silverstein, Dorit Barlevy, David H. Wasserman, Christine A. Walsh, Robert W. Marion, Siobhan M....> ;Journal of Genetic Counseling. 2015 Aug 1
• 12 citations
  Development of a Targeted Multi-Disorder High-Throughput Sequencing Assay for the Effective Identification of Disease-Causing Variants
  Maria Delio, Kunjan Patel, Alexander Y. Maslov, Robert W. Marion, Thomas V. McDonald, Evan M. Cadoff, Aaron Golden, John M. Greally, Jan Vijg, Bernice E. Morrow, Crist...> ;Plos One. 2015 Jul 27
• 12 citations
  Chromosome 22q11.2 Deletion Syndrome
  Elaine Pereira, Robert W. Marion> ;Pediatrics in Review. 2015 Jun 1
• 11 citations
  Psychological stress associated with cardiogenetic conditions
  Nadia Hidayatallah, Louise Bordeaux Silverstein, Marina Stolerman, Thomas V. McDonald, Christine A. Walsh, Esma Paljevic, Lilian L. Cohen, Robert W. Marion, David H. W...> ;Personalized Medicine. 2014 Nov 7
• 14 citations
  A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review.
  Deqiong Ma, Robert W. Marion, Netra Prasad Punjabi, Elaine Pereira, Joy M. Samanich, Chhavi Agarwal, Jianli Li, Chih Kang Huang, K. H. Ramesh, Linda A. Cannizzaro, Riz...> ;Molecular Cytogenetics. 2014 Nov 26
• 4 citations
  Translating Advances in Cardiogenetics Into Effective Clinical Practice
  Louise Bordeaux Silverstein, Marina Stolerman, Nadia Hidayatallah, Thomas V. McDonald, Christine A. Walsh, Esma Paljevic, Lilian L. Cohen, Robert W. Marion, David H. W...> ;Qualitative Health Research. 2014 Aug 11
• 78 citations
  Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder
  Esther R. Berko, Masako Suzuki, Faygel Beren, Christophe Lemetre, Christine M. Alaimo, R. Brent Calder, Karen Ballaban-Gil, Batya Gounder, Kaylee Kampf, Jill Kirschen,...> ;Plos Genetics. 2014 May 29
• 86 citations
  De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy
  Thomas D. Cushion, Alex R. Paciorkowski, Daniela T. Pilz, Jonathan G. L. Mullins, Laurie E. Seltzer, Robert W. Marion, Emily Tuttle, Dalia Ghoneim, Susan L. Christian,...> ;American Journal of Human Genetics. 2014 Apr 3
• 15 citations
  Motivation to Pursue Genetic Testing in Individuals with a Personal or Family History of Cardiac Events or Sudden Cardiac Death
  Kathleen E. Erskine, Nadia Hidayatallah, Christine A. Walsh, Thomas V. McDonald, Lilian L. Cohen, Robert W. Marion, Siobhan M. Dolan> ;Journal of Genetic Counseling. 2014 Mar 25
• 110 citations
  Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  Maria Delio, Tingwei Guo, Donna M. McDonald-McGinn, Elaine H. Zackai, Sean Herman, Mark Kaminetzky, Anne Marie Higgins, Karlene Coleman, Carolyn Chow, Maria Jarlbrzkow...> ;American Journal of Human Genetics. 2013 Mar 7
• 16 citations
  Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams–Beuren syndrome
  Maria Delio, Kathleen Pope, Tao Wang, Joy Samanich, Chad R. Haldeman-Englert, Paige Kaplan, Tamim H. Shaikh, Jinlu Cai, Robert W. Marion, Bernice E. Morrow, Melanie Ba...> ;American Journal of Medical Genetics. Part A. 2013 Mar 1
• 19 citations
  An interdisciplinary approach to personalized medicine: case studies from a cardiogenetics clinic.
  Kathleen E. Erskine, Eleanor Griffith, Nicole DeGroat, Marina Stolerman, Louise Bordeaux Silverstein, Nadia Hidayatallah, David H. Wasserman, Esma Paljevic, Lilian L. ...> ;Personalized Medicine. 2013 Jan 1
• 15 citations
  Hepatoblastoma in a mosaic trisomy 18 patient.
  Elaine Maria Pereira, Robert W. Marion, K. H. Ramesh, Jane S. Kim, Michelle Ewart, Rosanna Ricafort> ;Journal of Pediatric Hematology/oncology. 2012 May 1
• 40 citations
  Genotype-phenotype correlation in interstitial 6q deletions: A report of 12 new cases
  Jill A. Rosenfeld, Dina Amrom, Eva Andermann, Frederick Andermann, Martin Veilleux, Cynthia J. Curry, Jamie Fisher, Arthur S. Aylsworth, Cynthia M. Powell, Kandamurugu...> ;Neurogenetics. 2012 Jan 5
• 2 citations
  17q12 Deletion in a patient with Williams syndrome: Case report and review of the literature.
  Lilian L. Cohen, Joy Samanich, Quilu Pan, Lakshmi Mehta, Robert W. Marion> ;Journal of Pediatric Genetics. 2012 Jan 1
• Two miracles, one year later
  Robert W. Marion> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2009 May 15
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Journal Articles

• Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder  
  Berko E, Suzuki M, Beren F, Lemetre C, Alaimo CM, Calder RB, Ballaban-Gil K, Gounder B, Kampf K, Kirschen J, Maqbool SB, Momin Z, Reynolds DM, Russo N, Shulman L, Sta..., PLoS Genet, 1/29/2014
• Motivation to pursue genetic testing in individuals with personal and family history of cardiac events or sudden cardiac death  
  Erskine KE, Hidayatallah NZ, Silverstein LB, Walsh CA, McDonald TV, Cohen L, Marion RW, Dolan SM, J Genet Counsel, 1/25/2014
• More than skin deep: Genetics, clinical manifestations and diagnosis of Albinism  
  Gittler JK, Marion R, Einstein Journal of Biology and Medicine, 1/16/2014
• De novo mutations in a novel beta-tubulin gene, TUBB2A, cause simplified gyral patterning and infant-onset epilepsy  
  Cushion TD, Paciorkowski AR, Mullins JGL, Seltzer LE, Marion RW, Tuttle E, Ghoneim D, Christian SL, Pilz DT, Chung S-K, Rees MI, Dobyns WB, Am J Human Genetics, 1/1/2014
• Psychological stress associated with cardiogenetic conditions  
  Hidayatallah N, Silverstein LB, Stolerman M, McDonald TV, Walsh CA, Paljevic E, Cohen LL, Marion RW, Wasserman D, Hreyo S, Dolan SM, Personalized Medicine, 1/1/2014
• A de novo 1079 Mb interstitial deletion at 2q13q142 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review  
  Ma D, Punjabi NP, Pereira E, Samanich J, Agarwal C, Li Chih-Kang Huang J, Ramesh KH, Cannizzaro LA, Marion RW, Naeem R, Molecular Cytogenetics, 1/1/2014
• Enhanced maternal origin of the 22q112 deletion in velo-cardio-facial/DiGeorge syndrome  
  Delio M, Morrow BE, Guo T…Marion R…Shprintzen RJ, Emanuel BS, Am J Human Genetics, 1/1/2013
• Elastin sequence variants and cardiovascular phenotype in 54 Wlliams-Beuren syndrome patients  
  Delio M, Pope K, Wang T, Samanich J, Marion RW, Shaikh T, Cai J, Morrow BE, Babcock M, Am J Med Genetics, 1/1/2013
• An Interdisciplinary Approach to Personalized Medicine: Case Studies from a Cardiogenetics Clinic  
  Erskine KE, Griffith E, DeGroat N,Stolerman M, Silverstein LB, Hidayatallah N, Wasserman, D, Paljevic E, Cohen L,Walsh CA, McDonald TV, Marion RW, Dolan SM, Personalized Medicine, 1/1/2013
• Perceptions of an Implantable Cardioverter-Defibrillator: A Qualitative Study of Families with a History of Sudden, Life-Threatening Cardiac Events, and Recommendation...  
  Linder J, Hidayatallah N, Stolerman M, McDonald TV, Marion R, Walsh C, Dolan SM, Einstein J of Biol Med, 1/1/2013
• Perceptions of an Implantable Cardioverter-Defibrillator: A Qualitative Study of Families with a History of Sudden, Life-Threatening Cardiac Events, and Recommendation...  
  Linder J, Hidayatallah N, Stolerman M, McDonald TV, Marion R, Walsh C, Dolan SM, Einstein J of Biol Med, 1/1/2013
• Genotype-phenotype correlation in interstitial 6q deletions: A report of 12 new cases  
  Rosenfeld JA, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, Fisher J et al, Neurogenetics, 2/1/2012
• Genotype–phenotype correlation in interstitial 6q deletions: A report of 12 new cases  
  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..., Neurogenetics, 1/1/2012
• 17q12 Deletion in a Williams Syndrome Patient: Case Report and Review of the Literature  
  Cohen LL, Samanich J, Marion RW, J Ped Genet, 1/1/2012
• Brief Report: Hepatoblastoma in a mosaic type trisomy 18 patient  
  Pereira EM, Marion R, Ramesh KH, Kim J, Ewart M, Ricafort R, J Pediatr Hematol Oncol, 1/1/2012
• Judicial spectrum primer: What judges need to know about children with autism spectrum disorders  
  Dicker S, Marion R, Juvenile and Family Court Journal, 1/1/2012
• Two miracles, one year later  
  Marion RW, Am J Med Genetics Part C Semin Med Genet, 1/1/2009
• Two miracles, one year later  
  Marion RW, Am J Med Genetics, 1/1/2009
• Diversity in genetic counseling: strategies from the LEND network  
  Hatchel A, Willis J, Reiser C, Marion R, Pariseau C, Vanner-Nicely L, Bodurtha J, J Genet Couns, 1/1/2009
• A flat head in a round world: Dispelling common myths about plagiocephaly  
  Polotsky A, Shur N, Marion R, The Female Patient, 1/1/2007
• A surprising postnatal diagnosis  
  Shur N, Marion R, Gross SJ, Obstet Gynecol, 1/1/2006
• Prenatal diagnosis of Marshall syndrome by targeted sonography  
  Iacoboni D, Karpel BM, Shanske AL, Marion RW, Gross SJ, J Ultrasound Med, 1/1/2005
• Genetic Drift: September 11; 3:00 PM  
  Marion RW, Am J Med Genet, 1/1/2003
• First trimester diagnosis of Bartsocas Papas syndrome by transvaginal ultrasound: Case report and review of the literature  
  Dolan S, Gross S, Marion R, Shanske S, Prenat Diagn, 1/1/2003
• First trimester diagnosis of Bartsocas Papas syndrome by transvaginal ultrasound: Case report and review of the literature  
  Dolan S, Gross S, Marion R, Shanske S, Prenat Diagn, 1/1/2003
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Books/Book Chapters

• Neonatology for Primary Care 
  Chapter: Common Congenital Anomalies 
  Page 283 - 300Rosen O, Marion RW, Samanich JMEditors: Campbell DE.American Academy of Pediatrics2015
• 22q11.2 Deletion Syndrome: Tracking a Rare Genetic Disease in the Bronx 
  Marion R, Morrow B2014
• Passing the Torch with Passion and a Memento 
  Marion RW2013
• The $1,000 Genome and the Million-Dollar Question 
  Marion RW2013
• Rebuttal: Folic Acid Exposure a Fair Price to Pay for Healthy Babies 
  Marion RW2013
• On Retirement: Thoughts of An Academic Physician 
  Marion RW2013
• Genetic Round: A Doctor’s Encounters in the Field That Revolutionized Medicine 
  Chapter: Kaplan Publishing Company 
  Marion RWNew York, NY2009
• Teaching Cases Exploring Cross-Cultural Care 
  Chapter: Sociocultural aspects of working with a family affected with a rare autosomal recessive condition 
  Dolan S, Marion REditors: Silberman S, Correa N, Strelnick AH, Townsend J and Spano H.CREED, Bronx, NY2007
• The Intern Blues: The Timeless Classic About the Making of a Doctor 
  Marion RWHarperPerrenial, New York, NY2001
• Encounters in Microbiology 
  Chapter: The baby who stopped eating 
  Page 53 - 60Marion RWEditors: Alcamo IE.Jones & Bartlett Publishers, Boston, MA2001
• Comprehensive Adolescent Health Care 
  Chapter: The Approach to the Adolescent with a Genetic Disorder 
  Marion R, Schneider MEditors: Friedman SB, Fisher M, Schonberg SK.Quality Medical Publishing, St. Louis, MOEdition 2nd,1997
• Rotations: The Twelve Months of Intern Life 
  Marion RWHarper Collins Publ Co, New York, NY1997
• Clinical Manual of Emergency Pediatrics 
  Chapter: Genetic Emergencies 
  Page 249 - 254Marion RWEditors: Crain EF, Gershel JC, and Gallagher EJ.McGraw Hill, New York, NYEdition 3rd,1996
• Pediatrics for Medical Students 
  Chapter: Genetics 
  Page 417 - 436Marion RWEditors: Shelov SP and Bernstein D.Williams and Wilkins, Baltimore, MD1996
• Primary Pediatric Care 
  Chapter: Umbilical anomalies 
  Marion RWEditors: Hoekelman RA.Mosby-Year Book, Inc, St. Louis, MO1996
• Emergency Room: Lives Saved and Lost: Doctors Tell Their Stories 
  Chapter: Halloween 
  Page 179 - 183Marion RWEditors: Sachs D.Little Brown, Boston, MA1996
• Cleft palate 
  Bogdanow A, Menasse-Palmer L, Shanske AL, Marion RW1995
• Choanal atresia 
  Menasse-Palmer L, Bogdanow A, Marion RW1995
• Why the father of our country was childless 
  Marion RW1994
• Was George Washington Really the Father of our Country? A Clinical Geneticist Looks at World History 
  Marion RWAddison-Wesley Publishing Co, New York, NY1994
• Ladies Home Journal's Parent Digest 
  Chapter: Kevin's Question 
  Page 30 - 33Marion RW1994
• From the Heart: Stories by Mothers of Children With Special Needs 
  Chapter: Forward: What Doctors Think Patients Want From Their Doctors 
  Marion RWEditors: Bowman P, Grady M, Kendrick M, Ladew-Duncan J, Mentzer S, Newman R, Pease R, Son K, Spadinger L.U Southern Maine Press, Portland, ME1994
• Im Spiegel der Zeit: Das Beste 
  Chapter: Learning to Play God: The Coming of Age of aYoung Doctor 
  Marion RWFawcett Crest, New York, NY1993
• Dialogues in Pediatric Urol 
  Chapter: Syndromes associated with vaginal and uterine malformations 
  Marion RWEditors: Tenenbaum S.1993
• Reproductive Risks and Prenatal Diagnosis 
  Chapter: The Assessment and Management of Neonates With Congenital Anomalies 
  Page 341 - 358Marion RW and Fleischman, AREditors: Evans, M.Appleton, Lange, Norwalk, CT1992
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Abstracts/Posters

• Trying to unravel the etiology of multiple midline congenital anomalies misdiagnosed as VACTERL
  Pereira EM, Ramos MP, Greally JM, Marion RW, Am Soc Human Genetics, 63rd annual meeting, Boston, MA, 1/1/2013
• Epigenetic dysregulation of ectodermal cells in autism spectrum disorder
  Berko ER, Suzuki M, Beren F,…Marion RW…Greally JM, Am Soc Human Genetics, 63rd annual meeting, Boston, MA, 1/1/2013
• Music for Intervention: A Common Link Working with a Diverse Group, a focus on Williams Syndrome
  Terilli C, Kirschner L, Shall S, Pharr C, Marion R, Association of University Centers on Disabilities annual meeting, Washington, D.C., 1/1/2013
• Maternal age distribution at the time of birth of children with autism spectrum disorder
  Marion R, Valicenti-McDermott R,M, Grider T, Burrows B, PAS Annual Meeting, Vancouver, BC, Canada, 1/1/2010
• Enabling community participation for adults with spina bifida in the Bronx
  Ridgway E, Kornhaber L, Siegel, J, Cantres L, Marion R, ASB, 1/1/2010
• Arrhythmogenic biophysical phenotype for SCN5A mutation S1787N depends upon splice variant background and low pH
  Tan B-H, Song C, Tester DJ, Zhou Q, Marion RW, McDonald TV, Ackerman MJ, Makielski JC, American Heart Association Annual Meeting, 1/1/2010
• Ethical and social implication of genetic testing in the case of unexpected deaths: Translational of cardiogenic knowledge to clinical practice
  Dolan SM, Marion RW, McDonald TV, Wasserman D, International Conference on Perinatal and Infant Death Annual Meeting, Washington, D.C., 1/1/2010
• Ethical, legal, and social implications of genetic testing in the case of unexpected deaths: The translation of cardiogenetic knowledge to clinical practice
  DeGroat N, Cohen L, Marion RW, Walsh CA, McDonald TV, Dolan SM, 4th National Conference on Genomics and Public Health: Using Genomic Information to Improve Health Now and in the Future, 1/1/2010
• Cardiogenetics: Developing a Model for Successful Implementation of Personalized Genetic Medicine
  McDermott DA, Cohen LL, Dolan SM, Marion R, ASHG annual meeting, Washington, D.C., 1/1/2010
• Copy number variations associated with developmental disorders in a Bronx minority population
  Babcock M, Samanich J, Marion RW, Levy P, Shanske A, Pope K, Yachelevich N, Hsu DT, Pan Q, Huang KT, Cannizzaro L, Ramesh KH, Montagna C, Flynn L, Morrow BE, American Soc Human Genetics 59th annual meeting, Honolulu, HI, 1/21/2009
• Advancing maternal age in children with an Autism Spectrum Disorder and Language Regression
  Valicenti-McDermott M, Burrows B, Tibbetts J, Marion R, Shulman L, PAS annual meeting, Honolulu, HI, 1/1/2008
• Caring for families at risk for sudden death (SD): The organization and early outcomes of a multidisciplinary cardiogenetics clinic
  Pope KO, Paljevic ED, Walsh CA, McDonald T, Marion RW, American Society of Human Genetics 58th Annual Meeting, Philadelphia, PA, 1/1/2008
• The Geneticist’s view of Legg-Calve-Perthes Disease: A Case Report that Suggests the Need to Screen for Inherited Thrombophilias
  Shur N, Marion R, American College of Medical Genetics meeting, FL, 1/1/2007
• A Southern Italian CFTR mutation in a Jordanian girl with cystic fibrosis (CF)
  Samanich J, Fiorino E, Vicencio A, Marion R, American College of Medical Genetics meeting, FL, 1/1/2007
• The Spina Bifida Clinic at Blythedale: A 20 year perspective
  Marion R, Schendel, L, Goodrich J, Seimon L, Kogan S, Borkow R, Am Soc Human Genetics 57th Annual Meeting, San Diego, CA, 1/1/2007
• An unusual finding in a child with a presumably balanced 11:22 translocation: The importance of array CGH
  Shur N, Marion R, Greally J, Am Soc Human Genetics 57th Annual Meeting, San Diego, CA, 1/1/2007
• The Spina Bifida Clinic at Blythedale: A 20 year perspective
  Marion RW, AUCD annual meeting, Washington, D.C., 1/1/2007
• A novel pathologic variant in the WFS1 gene in a patient with Wolfram syndrome
  Marion R, Shur N, Peeters N, Wuyts W, Am College of Medical Genetics meeting, San Diego, CA, 1/25/2006
• The potential for false reassurance in prenatal care: The case of a 37 year old woman with a normal quad screen and a baby born with Down syndrome
  Shur N, Dolan S, Klugman S, Gross S, Marion R, Am College of Medical Genetics meeting, San Diego, CA, 1/24/2006
• An atypical presentation of systemic epidermal nevus syndrome in childhood
  Shur N, Marion R, Samanich J, Schaffer J, Roe A, Am Soc Human Genetics 56th Annual Meeting, New Orleans, LA, 1/10/2006
• The “Genetic Picture of the Week” Contest: An interactive method for teaching syndromes to residents
  Samanich J, Shur N, Marion R, PAS meetings, San Francisco, CA, 1/1/2006
• Staged separation of craniopagus conjoined twins: Medical and neurodevelopmental follow-up one year after separation
  Marion R, Goodrich J, Staffenberg D, Am Soc Human Genetics 55th Annual Meeting, Salt Lake City, UT, 1/25/2005
• Teaching genomic medicine to third year medical students: The Einstein experience
  Marion R, Campbell C, Am J Human Genet; Am Soc Human Genetics meeting, Los Angeles, CA, 1/1/2003
• Rhizomelic chondrodysplasia punctata and maternal autoimmune disease: A new case and review of the literature
  Shur N, Marion R et al, Am J Human Genet; Am Soc Human Genetics meeting, Los Angeles, CA, 1/1/2003
• Atypical phenotype associated with del 18q21.31: Case study and review of the literature
  Barbouth D, Zohouri M, Ramesh KH, Cannizzaro LA, Pulijaal VR, Marion RW, Am J Hum Genet; Am Soc Hum Genetics meeting, Los Angeles, CA, 1/1/2003
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Other

• The Burden of the Medical Geneticist: Does a Doctor Ever Stop Diagnosing? 
  Marion RW, The Doctor’s Tablet
  http://blogs.einstein.yu.edu/the-burden-of-the-medical-geneticist-does-a-doctor-ever-stop-diagnosing-2/#sthash.j6hes98j.dpuf
  1/17/2012
• Einstein Editions: Genetic Rounds: A Doctor’s Encounters in the Field that Revolutionized Medicine 
  Marion RW, Einstein: The Magazine for Alumni and Friends of the Albert Einstein College of Medicine of Yeshiva
  1/1/2010
• Personalized Medicine: The Future is Now – or at least very soon. HealthWorks: Medicine, Prevention, Wellness 
  Marion RW, The Journal News
  1/1/2010
• Autism Spectrum Disorder and the Clinical Geneticist: An Approach to the Family 
  Marion RW, Autism Spectrum News
  1/1/2009
• Two Miracles, One Year Later 
  Marion RW
  1/1/2006
• Review of The Soul of A Doctor: Harvard Medical Students Face Life and Death 
  Marion RW
  1/1/2006
• Workshop: Teaching Genomic Medicine to Pediatric Clerks: The Future is now! 
  Miller S, Marion RW et al, Pediatric Academic Society meetings
  San Francisco, CA - 1/4/2004
• Growing old quickly in the Bronx. E=MD2 
  Marion RW, The Alumni Magazine of the Albert Einstein College of Medicine
  1/1/2003
• Vital Signs: The curse of the Garcias 
  Marion RW, Discover magazine
  1/1/2000
• Vital Signs: A case of abuse 
  Marion RW, Discover magazine
  1/1/1999
• Vital Signs: Andrew of the Dark 
  Marion RW, Discover magazine
  1/1/1997
• Im Dienst des Lebens: Meine Anfangsjahre als Arzt 
  Marion RW, Reader's Digest
  Stuttgart, Germany - 1/1/1995
• Vital Signs: The Girl Who Mewed 
  Marion RW, Discover magazine
  1/1/1995
• Vital Signs: A Cry from the Brain 
  Marion RW, Discover magazine
  1/1/1995
• Andrew's parents 
  Marion RW, Hippocrates
  1/1/1993
• Life and Death 101 
  Marion RW, Physician (Montefiore Medical Center)
  1/1/1992
• Doctor to doctor: Following an intern through his first month 
  Marion RW, Career Insights M.D.
  1/1/1992
• The Mystery of Cassandra 
  Marion RW, The Saturday Evening Post
  1/1/1991
• Alex Goes for a Walk 
  Marion RW, Reader's Digest
  1/1/1990
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