Holly K. Tabor
Stanford University
99 Papers
512 Citations
Holly K. Tabor is an academic researcher from Stanford University. The author has contributed to research in topics: Exome sequencing & Medicine. The author has an hindex of 36, co-authored 74 publications. Previous affiliations of Holly K. Tabor include University of Washington & University of California, San Francisco.
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Papers
Continuing a search for a diagnosis: the impact of adolescence and family dynamics
Ilana M. Miller,Beverly M. Yashar,Maria T. Acosta,Margaret P Adam,David H. Adams,Pankaj B. Agrawal,Justin Alvey,Laura M. Amendola,Ashley Andrews,Euan A. Ashley,Mahshid S. Azamian,Carlos A. Bacino,Guney Bademci,E. Baker,Ashok Balasubramanyam,Dustin Baldridge,James F. Bale,Michael J. Bamshad,Deborah Barbouth,Pinar Bayrak-Toydemir,Anita E. Beck,Alan H. Beggs,Edward M. Behrens,Gill Bejerano,Hugo J. Bellen,Jimmy Bennett,Beverly Berg-Rood,Jonathan A. Bernstein,Gerard T. Berry,Anna Bican,Stephanie Bivona,Elizabeth E. Appel Blue,John Bohnsack,Carsten Bonnenmann,Devon Bonner,Lorenzo Botto,Brenna N. Boyd,Lauren C. Briere,Elly Brokamp,Gabrielle Brown,Elizabeth A. Burke,Lindsay C. Burrage,Manish J. Butte,Peter H. Byers,William E. Byrd,John C. Carey,Olveen Carrasquillo,Ta Chen Peter Chang,Sirisak Chanprasert,Hsiao-Tuan Chao,Gary D. Clark,Terra R. Coakley,Laurel A. Cobban,Joy D. Cogan,Matthew Coggins,F. Sessions Cole,Heather A. Colley,Cynthia M. Cooper,Heidi Cope,William J. Craigen,Andrew B. Crouse,Michael L. Cunningham,Precilla D'Souza,Hongzheng Dai,Surendra Dasari,Joie Davis,Jyoti G. Dayal,Esteban C. Dell'Angelica,Katrina M. Dipple,Daniel T. Doherty,Naghmeh Dorrani,A Doss,Emilie D. Douine,David D. Draper,Laura Duncan,D. Earl,David J. Eckstein,Lisa Emrick,Christine M. Eng,Cecilia Esteves,Marni J. Falk,Liliana Fernandez,Carlos Ferreira,Elizabeth L. Fieg,Laurie Findley,Paul B. Fisher,Brent L. Fogel,Irman Forghani,William A. Gahl,Ian Glass,Bernadette L. Gochuico,Rena A. Godfrey,Katie Golden-Grant,Madison Goldrich,David Goldstein,Alana L. Grajewski,Catherine Groden,Irma Gutierrez,Sihoun Hahn,Rizwan Hamid,Kelly Hassey,Nichole Hayes,Frances A. High,Anne Hing,Fuki M. Hisama,Ingrid A. Holm,Jason Hom,Martha Horike-Pyne,Yong Huang,Alden Y. Huang,Laryssa A. Huryn,Rosario Isasi,Kosuke Izumi,Fariha Jamal,Gail P. Jarvik,Jeffrey G. Jarvik,Suman Jayadev,Lefkothea P. Karaviti,Jennifer A. Kennedy,Shamika Ketkar,Dana Kiley,Gonench Kilich,Shilpa Nadimpalli Kobren,Isaac S. Kohane,Jennefer N. Kohler,Susan A. Korrick,Mary Kozuira,Deborah Krakow,Donna M. Krasnewich,Elijah Kravets,Joel B. Krier,Seema R. Lalani,Byron L. Lam,Christina Lam,Grace L. LaMoure,Brendan C. Lanpher,Ian R. Lanza,Lea Latham,Kimberly H. LeBlanc,Brendan Lee,Han-Rei Lee,R. Levitt,Richard A. Lewis,Sharyn A. Lincoln,Pengfei Liu,X.-Z. Liu,Nicola Longo,Sandra K. Loo,Joseph Loscalzo,Richard L. Maas,J MacDowall,Ellen Macnamara,Calum A. MacRae,Valerie Maduro,Rachel Mahoney,Bryan C Mak,May Christine V. Malicdan,Laura A. Mamounas,Teri A. Manolio,Rong Mao,Kenneth R. Maravilla,Thomas C. Markello,Ronit Marom,Gabor T. Marth,Beth A. Martin,Martin G. Martin,Shruti Marwaha,Jacob L. McCauley,Allyn McConkie-Rosell,Alexa T. McCray,Elisabeth McGee,Heather C Mefford,J. Lawrence Merritt,Matt Might,Ghayda M. Mirzaa,Eva Morava,Paolo Moretti,P. Moretti,Deborah Mosbrook-Davis,John J. Mulvihill,Mariko Nakano-Okuno,Avindra Nath,Stanley F. Nelson,J. H. Newman,Sarah K. Nicholas,Deborah A. Nickerson,Shirley Nieves-Rodriguez,Donna Novacic,Devin Oglesbee,James P. Orengo,Laura Pace,Stephen Pak,J. Carl Pallais,Christina G.S. Palmer,Jeanette C. Papp,Neil H. Parker,John A. Phillips,Jennifer E. Posey,Lorraine Potocki,Bradley Power,Barbara N. Pusey,Aaron R. Quinlan,Archana Raja,Deepak A. Rao,A Raper,Wendy H. Raskind,Genecee Renteria,Chloe M. Reuter,Lynette Rives,Amy K. Robertson,Lance H. Rodan,Jill A. Rosenfeld,Natalie Rosenwasser,Francis Rossignol,Maura R.Z. Ruzhnikov,Ralph L. Sacco,Jacinda B. Sampson,Mario Saporta,Judith L. Schaechter,Timothy Schedl,Kelly Schoch,Daryl A. Scott,C. Ron Scott,Vandana Shashi,Jimann Shin,Rebecca Signer,Edwin K. Silverman,Janet S. Sinsheimer,Kathleen Sisco,Edward Curtis Smith,Kevin S Smith,Emily Solem,Lilianna Solnica-Krezel,Ben Solomon,Rebecca C. Spillmann,Joan M. Stoler,Kathleen Sullivan,Jennifer A. Sullivan,Angela Sun,Shirley Sutton,David A. Sweetser,Virginia P. Sybert,Holly K. Tabor,Queenie K.-G. Tan,Amelia L.M. Tan,Mustafa Tekin,Fred F. Telischi,Willa Thorson,Audrey Thurm,Cynthia J. Tifft,Camilo Toro,Alyssa A. Tran,Brian Tucker,Tiina K. Urv,Adeline Vanderver,Matt Velinder,David Viskochil,Tiphanie P. Vogel,Colleen E. Wahl,Melissa A. Walker,Stephanie Wallace,Nicole M. Walley,Christopher A. Walsh,Jennifer A. Wambach,Jijun Wan,Lee-kai Wang,Michael F. Wangler,Patricia A. Ward,Daniel J. Wegner,Monika Weisz Hubshman,Mark H. Wener,Tara Wenger,Katherine Wesseling Perry,Monte Westerfield,Matthew T. Wheeler,Jordan H. Whitlock,Lynne A. Wolfe,Jeremy D. Woods,Kim A. Worley,Shinya Yamamoto,John Yang,Muhammad Yousef,Diane B. Zastrow,Wadih M. Zein,Zhenyu Zhang,Chunli Zhao,Stephan Zuchner +286 more
TL;DR: Pelentsov et al. as mentioned in this paper investigated how families of children with undiagnosed diseases decide whether to continue to pursue a diagnosis after standard clinical testing has failed and found that alignment or misalignment of parent and child needs impact the trajectory of the diagnostic search.
3
Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families.
Fernanda Delgado,Holly K. Tabor,Penny Chow,Jessie H. Conta,Kenneth W. Feldman,Karen D. Tsuchiya,Anita E. Beck +6 more
TL;DR: As single-nucleotide polymorphism arrays become a common clinical diagnostic tool, clinicians can use this framework to return results of unexpected consanguinity to families in a supportive and productive manner.
3
Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features
Jessica X. Chong,Joon Ho Yu,Peter Lorentzen,Karen M. Park,Seema M. Jamal,Holly K. Tabor,Anita Rauch,Margarita Saenz,Eugen Boltshauser,Karynne E. Patterson,Deborah A. Nickerson,Michael J. Bamshad +11 more
TL;DR: The Repository for Mendelian Genomics Family Portal (RMD-FP) as discussed by the authors was developed to facilitate the efforts of families to share phenotypic and genomic information with each other, clinicians, and researchers.
Unanticipated results from exome sequencing/whole genome sequencing: The sky won't fall†
TL;DR: It is argued that the pace at which ES/WGS is being used in research and clinical settings is accelerating, coincident with rapidly improving and maturing sequencing, analytical, annotation, and reporting pipelines, which will lead to the more frequent identification of unanticipated variants of clinical utility.
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"Women Who Don't Give a Crap".
TL;DR: Four books about women in science, past and present that PLOS Genetics readers, irrespective of gender or generation, will also find stories and ideas in these books that connect to their own professional and personal experiences.