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David A. Stevenson

Stanford University

43H-index
258Paper Count
8.0KCitation Count
Published Papers 46
Publication Date
Influences of RASopathies on Neuroanatomical Variation in Children
err2024-09-01
err2
PREAI
errMcghee, Chloe Alexa; Honari, Hamed; Siqueiros-Sanchez, Monica; Serur, Yaffa; Staalduinen, Eric K. van; Stevenson, David; Bruno, Jennifer L.; Raman, Mira Michelle; Green, Tamar
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Diazoxide choline extended-release tablet in people with Prader-Willi syndrome: results from long-term open-label study
errOBESITY
IF4.7
err2023-11-02
err2
errOAAI
errMiller, Jennifer L.; Gevers, Evelien; Bridges, Nicola; Yanovski, Jack A.; Salehi, Parisa; Obrynba, Kathryn S.; Felner, Eric I.; Bird, Lynne M.; Shoemaker, Ashley H.; Angulo, Moris; Butler, Merlin G.; Stevenson, David; Goldstone, Anthony P.; Wilding, John; Lah, Melissa; Shaikh, M. Guftar; Littlejohn, Elizabeth; Abuzzahab, M. Jennifer; Fleischman, Amy; Hirano, Patricia; Yen, Kristen; Cowen, Neil M.; Bhatnagar, Anish
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Frequency of epistaxis and telangiectasia in patients with hereditary hemorrhagic telangiectasia (HHT) in comparison with the general population: Cura,cao diagnostic criteria revisited
err2023-08-01
err8
errOAAI
errMcDonald, Jamie; Kornish, Jenna; Stevenson, David A.; Hanson-Kahn, Andrea; Balch, Heather; James, John; Naik, Hetanshi; Whitehead, Kevin J.
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Papillomas of Costello syndrome are not associated with human papillomavirus infection in a small case series
err2023-08-01
err1
PREAI
errOlsen, Gerilyn M.; Johnson, Luke; Castel, Pau; Stevenson, David A.; White, Kevin; Chiu, Yvonne E.; Krol, Alfons; Siegel, Dawn H.
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Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled Trial
err2023-01-14
err16
errOAAI
errMiller, Jennifer L.; Gevers, Evelien; Bridges, Nicola; Yanovski, Jack A.; Salehi, Parisa; Obrynba, Kathryn S.; Felner, Eric, I; Bird, Lynne M.; Shoemaker, Ashley H.; Angulo, Moris; Butler, Merlin G.; Stevenson, David; Abuzzahab, Jennifer; Barrett, Timothy; Lah, Melissa; Littlejohn, Elizabeth; Mathew, Verghese; Cowen, Neil M.; Bhatnagar, Anish
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Factors associated with the time to complete clinical exome sequencing in a pediatric patient population
err2022-10-01
err2
errOAAI
errLee, Gabriella; Yu, Linbo; Suarez, Carlos J.; Stevenson, David A.; Ling, Albee; Killer, Lindsay
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Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation
err2022-09-01
err90
errOAAI
errPlotkin, Scott R.; Messiaen, Ludwine; Legius, Eric; Pancza, Patrice; Avery, Robert A.; Blakeley, Jaishri O.; Babovic-Vuksanovic, Dusica; Ferner, Rosalie; Fisher, Michael J.; Friedman, Jan M.; Giovannini, Marco; Gutmann, David H.; Hanemann, Clemens Oliver; Kalamarides, Michel; Kehrer-Sawatzki, Hildegard; Korf, Bruce R.; Mautner, Victor-Felix; MacCollin, Mia; Papi, Laura; Rauen, Katherine A.; Riccardi, Vincent; Schorry, Elizabeth; Smith, Miriam J.; Stemmer-Rachamimov, Anat; Stevenson, David A.; Ullrich, Nicole J.; Viskochil, David; Wimmer, Katharina; Yohay, Kaleb; Huson, Susan M.; Wolkenstein, Pierre; Evans, D. Gareth
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Advances in the Understanding of Prader-Willi syndrome
err2022-08-01
err0
errOAAI
errStafford, Diane E. J.; Stevenson, David A.
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MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensus
err2022-07-05
err39
errOAAI
errde Blank, Peter M. K.; Gross, Andrea M.; Akshintala, Srivandana; Blakeley, Jaishri O.; Bollag, Gideon; Cannon, Ashley; Dombi, Eva; Fangusaro, Jason; Gelb, Bruce D.; Hargrave, Darren; Kim, AeRang; Klesse, Laura J.; Loh, Mignon; Martin, Staci; Moertel, Christopher; Packer, Roger; Payne, Jonathan M.; Rauen, Katherine A.; Rios, Jonathan J.; Robison, Nathan; Schorry, Elizabeth K.; Shannon, Kevin; Stevenson, David A.; Stieglitz, Elliot; Ullrich, Nicole J.; Walsh, Karin S.; Weiss, Brian D.; Wolters, Pamela L.; Yohay, Kaleb; Yohe, Marielle E.; Widemann, Brigitte C.; Fisher, Michael J.
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Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study
err2021-12-13
err7
errOAAI
errForde, Claire; Burkitt-Wright, Emma; Turnpenny, Peter D.; Haan, Eric; Ealing, John; Mansour, Sahar; Holder, Muriel; Lahiri, Nayana; Dixit, Abhijit; Procter, Annie; Pacot, Laurence; Vidaud, Dominique; Capri, Yline; Gerard, Marion; Dollfus, Helene; Schaefer, Elise; Quelin, Chloe; Sigaudy, Sabine; Busa, Tiffany; Vera, Gabriella; Damaj, Lena; Messiaen, Ludwine; Stevenson, David A.; Davies, Peter; Palmer-Smith, Sheila; Callaway, Alison; Wolkenstein, Pierre; Pasmant, Eric; Upadhyaya, Meena
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Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma
err2021-09-01
err3
errOAAI
errEvans, D. Gareth; Messiaen, Ludwine M.; Foulkes, William D.; Irving, Rachel E. A.; Murray, Alexandra J.; Perez-Becerril, Cristina; Rivera, Barbara; McDonald-McGinn, Donna M.; Stevenson, David A.; Smith, Miriam J.
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Response to Biesecker et al.
err2021-09-01
err0
errOAAI
errBiesecker, Leslie G.; Adam, Margaret P.; Alkuraya, Fowzan S.; Amemiya, Anne R.; Bamshad, Michael J.; Beck, Anita E.; Bennett, James T.; Bird, Lynne M.; Carey, John C.; Chung, Brian; Clark, Robin D.; Cox, Timothy C.; Curry, Cynthia; Dinulos, Mary Beth Palko; Dobyns, William B.; Giampietro, Philip F.; Girisha, Katta M.; Glass, Ian A.; Graham, John M., Jr.; Gripp, Karen W.; Haldeman-Englert, Chad R.; Hall, Bryan D.; Innes, A. Micheil; Kalish, Jennifer M.; Keppler-Noreuil, Kim M.; Kosaki, Kenjiro; Kozel, Beth A.; Mirzaa, Ghayda M.; Mulvihill, John J.; Nowaczyk, Malgorzata J. M.; Pagon, Roberta A.; Retterer, Kyle; Rope, Alan F.; Sanchez-Lara, Pedro A.; Seaver, Laurie H.; Shieh, Joseph T.; Slavotinek, Anne M.; Sobering, Andrew K.; Stevens, Cathy A.; Stevenson, David A.; Tan, Tiong Yang; Tan, Wen-Hann; Tsai, Anne C.; Weaver, David D.; Williams, Marc S.; Zackai, Elaine; Zarate, Yuri A.
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Reliability of Handheld Dynamometry to Measure Focal Muscle Weakness in Neurofibromatosis Types 1 and 2
err2021-08-17
err2
errOAAI
errAkshintala, Srivandana; Khalil, Nashwa; Yohay, Kaleb; Muzikansky, Alona; Allen, Jeffrey; Yaffe, Anna; Gross, Andrea M.; Fisher, Michael J.; Blakeley, Jaishri O.; Oberlander, Beverly; Pudel, Miriam; Engelson, Celia; Obletz, Jaime; Mitchell, Carole; Widemann, Brigitte C.; Stevenson, David A.; Plotkin, Scott R.
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Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation
err2021-08-01
err389
errOAAI
errLegius, Eric; Messiaen, Ludwine; Wolkenstein, Pierre; Pancza, Patrice; Avery, Robert A.; Berman, Yemima; Blakeley, Jaishri; Babovic-Vuksanovic, Dusica; Cunha, Karin Soares; Ferner, Rosalie; Fisher, Michael J.; Friedman, Jan M.; Gutmann, David H.; Kehrer-Sawatzki, Hildegard; Korf, Bruce R.; Mautner, Victor-Felix; Peltonen, Sirkku; Rauen, Katherine A.; Riccardi, Vincent; Schorry, Elizabeth; Stemmer-Rachamimov, Anat; Stevenson, David A.; Tadini, Gianluca; Ullrich, Nicole J.; Viskochil, David; Wimmer, Katharina; Yohay, Kaleb; Huson, Susan M.; Evans, D. Gareth; Plotkin, Scott R.
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A dyadic approach to the delineation of diagnostic entities in clinical genomics
err2021-01-01
err83
errOAAI
errBiesecker, Leslie G.; Adam, Margaret P.; Alkuraya, Fowzan S.; Amemiya, Anne R.; Bamshad, Michael J.; Beck, Anita E.; Bennett, James T.; Bird, Lynne M.; Carey, John C.; Chung, Brian; Clark, Robin D.; Cox, Timothy C.; Curry, Cynthia; Dinulos, Mary Beth Palko; Dobyns, William B.; Giampietro, Philip F.; Girisha, Katta M.; Glass, Ian A.; Graham, John M., Jr.; Gripp, Karen W.; Haldeman-Englert, Chad R.; Hall, Bryan D.; Innes, A. Micheil; Kalish, Jennifer M.; Keppler-Noreuil, Kim M.; Kosaki, Kenjiro; Kozel, Beth A.; Mirzaa, Ghayda M.; Mulvihill, John J.; Nowaczyk, Malgorzata J. M.; Pagon, Roberta A.; Retterer, Kyle; Rope, Alan F.; Sanchez-Lara, Pedro A.; Seaver, Laurie H.; Shieh, Joseph T.; Slavotinek, Anne M.; Sobering, Andrew K.; Stevens, Cathy A.; Stevenson, David A.; Tan, Tiong Yang; Tan, Wen-Hann; Tsai, Anne C.; Weaver, David D.; Williams, Marc S.; Zackai, Elaine; Zarate, Yuri A.
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Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome
err2021-01-01
err9
errOAAI
errWakeling, Emma; McEntagart, Meriel; Bruccoleri, Michael; Shaw-Smith, Charles; Stals, Karen L.; Wakeling, Matthew; Barnicoat, Angela; Beesley, Clare; Hanson-Kahn, Andrea K.; Kukolich, Mary; Stevenson, David A.; Campeau, Philippe M.; Ellard, Sian; Elsea, Sarah H.; Yang, Xiang-Jiao; Caswell, Richard C.
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Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort study
err2019-10-01
err15
errOAAI
errGonzalez, Cristian D.; Cipriano, Sarah D.; Topham, Christina A.; Stevenson, David A.; Whitehead, Kevin J.; Vanderhooft, Sheryll; Presson, Angela P.; McDonald, Jamie
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Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?
err2019-09-01
err43
errOAAI
errWooderchak-Donahue, Whitney L.; Akay, Gulsen; Whitehead, Kevin; Briggs, Eric; Stevenson, David A.; O'Fallon, Brendan; Velinder, Matthew; Farrell, Andrew; Shen, Wei; Bedoukian, Emma; Skrabann, Cara M.; Antaya, Richard J.; Henderson, Kate; Pollak, Jeffrey; Treat, James; Day, Ronald; Jacher, Joseph E.; Hannibal, Mark; Bontempo, Kelly; Marth, Gabor; Bayrak-Toydemir, Pinar; McDonald, Jamie
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Response to Hannah-Shmouni and Stratakis
err2019-05-01
err0
errOAAI
errStewart, Douglas R.; Korf, Bruce R.; Nathanson, Katherine L.; Stevenson, David A.; Yohay, Kaleb
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