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Dr. David Adams, MD


Dr. David Adams, MD


500 University Dr
500 University Dr
Hershey, PA 17033
 Get Directions
 Call: (800) 233-4082

Dr. David Adams, MD (he/him) is a Dermatologist in Hershey, PA with over 20 years of experience. What is your opinion of Dr. David Adams, MD? Rate this provider below so other people can make informed decision.



Gender
Male (Approximately 50% of Dermatologists in Hershey, PA are Male)



Degree Type
MD (Approximately 85% of Dermatologists in Hershey, PA have MD degree)



Medical Specialties
Dermatologist (There are 26 Dermatologists available in Hershey, PA, which is 4 times the average number of Dermatologists in similar U.S. locations)



Experience
20+ Years of Experience (About 27% more than the average Dermatologist in Hershey, PA)



Languages Spoken
English
Prescribed Medications
Triamcinolone Acetonide
Doxycycline Hyclate
Gabapentin
Methotrexate
Enbrel Sureclick (Generic Name: etanercept)
Metronidazole
Clobetasol Propionate
Betamethasone Dipropionate
Prednisone
Research Publications
Approximately 50% of Dermatologists in Hershey, PA have available research publications
Improved Identification of Large-effect Rare Genetic Variants using Haplotype Aggregated Allele-specific Expression Data.
Kaushik Ram Ganapathy, Martin Broly, Sarah Silverstein, Marcela Mendoza, Eric Song, Bence Kotis, Paul Hoffman, PCGC Consortium, Ali Torkamani, David R Adams, Carsten Bonnemann, Tuuli Lappalainen, Pejman Mohammadi
medRxiv : the preprint server for health sciences 2025-12-18
Phenotypic Variability and Paternal Inheritance of a CHD8 Variant Causing Intellectual Developmental Disorder With Autism and Macrocephaly Confirmed by Epigenetic and Structural Analyses.
Yutaka Furuta, Kimberly M Ezell, Rizwan Hamid, Joy D Cogan, Thomas A Cassini, Lynette Rives, Ashley McMinn, Shailee Shah, Amanda C Peltier, Stephen Layfield, Robin S Fletcher, Matthew L Tedder, Raymond J Louie, Jennifer A Lee, Jennifer Kerkhof, Jessica Rzasa, Bekim Sadikovic, Abdullah Al Mamun, Jonathan H Sheehan, Christopher W Moth, Jens Meiler, Marissa Vawter-Lee, Paola Maria Mendoza-Sengco, Jennifer B Holzen, Sumit Pruthi, John A Phillips, Rory J Tinker, Undiagnosed Diseases Network
Molecular genetics & genomic medicine 2025-12
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.
Sébastien Küry, Janelle E Stanton, Geeske M van Woerden, Amélie Bosc-Rosati, Tzung-Chien Hsieh, Lise Bray, Marielle Oloudé, Cory Rosenfelt, Marie Pier Scott-Boyer, Victoria Most, Tianyun Wang, Jonas J Papendorf, Charlotte de Konink, Wallid Deb, Virginie Vignard, Maja Studencka-Turski, Thomas Besnard, Anna M Hajdukowicz, Franziska G Thiel, Sophie Wolfgramm, Laëtitia Florenceau, Silvestre Cuinat, Sylvain Marsac, Yann Verrès, Audrey Dangoumau, Léa Poirier, Ingrid M Wentzensen, Annabelle Tuttle, Cara Forster, Johanna Striesow, Richard Golnik, Damara Ortiz, Laura Jenkins, Jill A Rosenfeld, Alban Ziegler, Clara Houdayer, Dominique Bonneau, Erin Torti, Amber Begtrup, Kristin G Monaghan, Sureni V Mullegama, Catharina M L Nienke Volker-Touw, Koen L I van Gassen, Renske Oegema, Mirjam S de Pagter, Katharina Steindl, Anita Rauch, Ivan Ivanovski, Kimberly McDonald, Emily Boothe, Andrew Dauber, Janice Baker, Noelle Andrea V Fabie, Raphael A Bernier, Tychele N Turner, Siddharth Srivastava, Kira A Dies, Lindsay C Swanson, Carrie Costin, Alali Abdulrazak, Rebekah K Jobling, John Pappas, Rachel Rabin, Dmitriy Niyazov, Anne Chun-Hui Tsai, Karen Kovak, David B Beck, May Christine V Malicdan, David R Adams, Lynne Wolfe, Rebecca D Ganetzky, Colleen C Muraresku, Davit Babikyan, Zdeněk Sedláček, Miroslava Hančárová, Andrew T Timberlake, Hind Al Saif, Berkley Nestler, Kayla King, M J Hajianpour, Gregory Costain, D'Arcy Prendergast, Chumei Li, David Geneviève, Antonio Vitobello, Arthur Sorlin, Christophe Philippe, Tamar Harel, Ori Toker, Ataf Sabir, Derek Lim, Mark J Hamilton, Lisa J Bryson, Elaine Cleary, Sacha Weber, Trevor L Hoffman, Anna M Cueto-González, Eduardo F Tizzano, David Gómez-Andrés, Marta Codina-Solà, Athina Ververi, Efterpi Pavlidou, Alexandros Lambropoulos, Kyriakos Garganis, Marlène Rio, Jonathan Levy, Sarah J Langas, Anne M McRae, Mathieu K Lessard, Maria Daniela D'Agostino, Isabelle De Bie, Meret Wegler, Rami Abou Jamra, Susanne B Kamphausen, Viktoria Bothe, Lorraine Potocki, Eric Olinger, Yves Sznajer, Elsa Wiame, Michelle L Thompson, Molly C Schroeder, Catherine Gooch, Raphael A Smith, Arti Pandya, Larissa M Busch, Uwe Völker, Elke Hammer, Kristian Wende, Benjamin Cogné, Bertrand Isidor, Jens Meiler, Clémentine Ripoll, Stéphanie Bigou, Frédéric Laumonnier, Peter W Hildebrand, Evan E Eichler, Kirsty McWalter, Peter M Krawitz, Florence Roux-Dalvai, Ype Elgersma, Julien Marcoux, Marie-Pierre Bousquet, Arnaud Droit, Jeremie Poschmann, Andreas M Grabrucker, Francois V Bolduc, Stéphane Bézieau, Frédéric Ebstein, Elke Krüger
Nature communications 2025-11-26
An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser.
Isabelle B Cooperstein, Shruti Marwaha, Alistair Ward, Shilpa N Kobren, Jennefer N Carter, Undiagnosed Diseases Network, Matthew T Wheeler, Gabor T Marth
Genome medicine 2025-10-21
LONP1 Variants Are Associated With Clinically Diverse Phenotypes.
Randee E Young, Lu Qiao, Rebecca Hernan, David A Sweetser, Jessica L Waxler, Daryl A Scott, Tiana M Scott, Seema R Lalani, Mahshid S Azamian, Jill A Rosenfeld, Bret Bostwick, Lindsay C Burrage, Undiagnosed Diseases Network, Lance H Rodan, Bianca E Russell, Marina Dutra-Clarke, Michael Kruer, Somayeh Bakhtiarim, Hossein Darvish, David J Amor, Shamima Rahman, Karen Stals, Lisa Bradley, Susan Byrne, Leandra K Tolusso, Beatrix Wong, Laura Benedict, Kimberly Wallis, Kestutis Micke, Cindy Colson, Thomas Smol, Sabrina V Southwick, Kristen A Miller, Michelle L Kush, Odelia Chorin, Annick Rothschild, Wei Wang, Yufeng Shen, Wendy K Chung
Clinical genetics 2025-09-10
Case Series of Nizon-Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid-Triploid Mosaicism.
Russell Stewart, Kimberly M Ezell, Deanna S Bell, Brian Corner, Ashley McMinn, Joy D Cogan, Rizwan Hamid, Lynette Rives, John A Phillips, Nina Paddu, Gitanjali Srivastava, Ronit Marom, Farah A Ladha, Claudia Soler-Alfonso, Rachel Franciskovich, Mary Koziura, Sumit Pruthi, Gabriele Richard, Christina B Sheedy, Undiagnosed Diseases Network, Thomas Cassini
American journal of medical genetics. Part A 2025-08-21
BK channel activity in skin fibroblasts from patients with neurological disorder.
Ria L Dinsdale, Thomas R Middendorf, Deborah Disilvestre, David Adams, William Gahl, Ellen F Macnamara, Lynne Wolfe, Camilo Toro, Cynthia J Tifft, Andrea L Meredith
Channels (Austin, Tex.) 2025-08-10
Neurodevelopmental Phenotyping and Genotyping in the Pediatric National Institute of Health Undiagnosed Disease Program.
Dee Adedipe, Audrey Thurm, Lisa Joseph, Maria T Acosta, Ellen F Macnamara, Colby Chlebowski, Riley Kessler, Precilla D'Souza, Lynne Wolfe, Jean M Johnson, Tyra Estwick, John Yang, Paul R Lee, Jennifer Murphy, Camilo Toro, Thomas Markello, Dennis Carter, David R Adams, William A Gahl, Cynthia J Tifft
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2025-07-22
ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy.
Rhys Dore, Chu-Ting Chang, Amber Declève, Gloria Brunori, W Grant Ludlam, Alden Huang, Mojtaba Movahedinia, Nadirah S Damseh, Ijaz Anwar, Mohammad Yahya Vahidi Mehrjardi, Annelii Ny, Mehdi Khorrami, Majid Kheirollahi, Helen Frederiksen, Fatemeh Eghbal, Mohammad Reza Mirjalili, Mohammadreza Dehghani, Ehsan Ghayoor Karimiani, Sergey Oreshkov, Cesar Alves, Pasquale Striano, Mohnish Suri, Julian Martinez-Agosto, Muhammad Ansar, Muhammad Zahid, Samra Akram, Muhammad Ansar, Stanley F Nelson, Undiagnosed Diseases Network, Stylianos E Antonarakis, Henry Houlden, Daniëlle Copmans, Kirill A Martemyanov, Reza Maroofian
Genetics in medicine : official journal of the American College of Medical Genetics 2025-06-23
Investigating the Utility of Leukocyte Sialic Acid Measurements in Lysosomal Free Sialic Acid Storage Disorder.
Marya S Sabir, Laura Pollard, Lynne Wolfe, David R Adams, Carla Ciccone, Petcharat Leoyklang, Frances M Platt, Marjan Huizing, William A Gahl, May Christine V Malicdan
JIMD reports 2025-06-16
Previous Research Publications Previous Research Publications 1 ... 1 ...11 1112 1213 1314 1415 15 ... 16 ... 16 Next Research Publications Next Research Publications
Payments From Medical Companies
(These can include payments from pharmaceutical companies, medical device companies, and other companies.)
Dr. David Adams, MD has received over $17 in payments from medical companies (100% less than the average Dermatologist in Hershey, PA)
  • Over $17 in payments for Education (81% less than the average Dermatologist in Hershey, PA)
Regeneron Healthcare Solutions, Inc. - $17.40 payment for Education on 01/16/2018



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Location

Location

500 University Dr
Hershey, PA 17033
 Get Directions
 Call: (800) 233-4082

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