Repetitive Thoughts and Repetitive Behaviors in Williams Syndrome
Huston, John C., Thom, Robyn P., Ravichandran, Caitlin T., Mullett, Jennifer E., Moran, Carly, Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.
Published in Journal of autism and developmental disorders (01.02.2022)
Published in Journal of autism and developmental disorders (01.02.2022)
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Hypercalcemia in Patients with Williams-Beuren Syndrome
Sindhar, Sampat, BS, Lugo, Michael, BS, Levin, Mark D., MD, Danback, Joshua R., BS, Brink, Benjamin D., MS, Yu, Eric, BA, Dietzen, Dennis J., PhD, Clark, Amy L., DO, Purgert, Carolyn A., MD, PhD, Waxler, Jessica L., MS, Elder, Robert W., MD, Pober, Barbara R., MD, Kozel, Beth A., MD, PhD
Published in The Journal of pediatrics (01.11.2016)
Published in The Journal of pediatrics (01.11.2016)
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Personalized Genetic Risk Counseling to Motivate Diabetes Prevention: A randomized trial
GRANT, Richard W, O'BRIEN, Kelsey E, FLOREZ, Jose C, MEIGS, James B, WAXLER, Jessica L, VASSY, Jason L, DELAHANTY, Linda M, BISSETT, Laurie G, GREEN, Robert C, STEMBER, Katherine G, GUIDUCCI, Candace, PARK, Elyse R
Published in Diabetes care (01.01.2013)
Published in Diabetes care (01.01.2013)
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Glucose and lipid metabolism, bone density, and body composition in individuals with Williams syndrome
Shaikh, Sofia, Waxler, Jessica L., Lee, Hang, Grinke, Kathy, Garry, Jamie, Pober, Barbara R., Stanley, Takara L.
Published in Clinical endocrinology (Oxford) (01.11.2018)
Published in Clinical endocrinology (Oxford) (01.11.2018)
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Journal Article
Buspirone for the Treatment of Generalized Anxiety Disorder in Williams Syndrome: A Case Series
Thom, Robyn P., Keary, Christopher J., Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.
Published in Journal of autism and developmental disorders (01.02.2020)
Published in Journal of autism and developmental disorders (01.02.2020)
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Journal Article
Williams Syndrome Predisposes to Vascular Stiffness Modified by Antihypertensive Use and Copy Number Changes in NCF1
Kozel, Beth A, Danback, Joshua R, Waxler, Jessica L, Knutsen, Russell H, de las Fuentes, Lisa, Reusz, Gyorgy S, Kis, Eva, Bhatt, Ami B, Pober, Barbara R
Published in Hypertension (Dallas, Tex. 1979) (01.01.2014)
Published in Hypertension (Dallas, Tex. 1979) (01.01.2014)
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Brief Report: Major Depressive Disorder with Psychotic Features in Williams Syndrome: A Case Series
Valdes, Francisca, Keary, Christopher J., Mullett, Jennifer E., Palumbo, Michelle L., Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.
Published in Journal of autism and developmental disorders (01.03.2018)
Published in Journal of autism and developmental disorders (01.03.2018)
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A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
Mucha, Bettina E, Banka, Siddharth, Ajeawung, Norbert Fonya, Molidperee, Sirinart, Chen, Gary G, Koenig, Mary Kay, Adejumo, Rhamat B, Till, Marianne, Harbord, Michael, Perrier, Renee, Lemyre, Emmanuelle, Boucher, Renee-Myriam, Skotko, Brian G, Waxler, Jessica L, Thomas, Mary Ann, Hodge, Jennelle C, Gecz, Jozef, Nicholl, Jillian, McGregor, Lesley, Linden, Tobias, Sisodiya, Sanjay M, Sanlaville, Damien, Cheung, Sau W, Ernst, Carl, Campeau, Philippe M
Published in Genetics in medicine (01.05.2019)
Published in Genetics in medicine (01.05.2019)
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Altered body composition, lipedema, and decreased bone density in individuals with Williams syndrome: A preliminary report
Waxler, Jessica L, Guardino, Cara, Feinn, Richard S, Lee, Hang, Pober, Barbara R, Stanley, Takara L
Published in European journal of medical genetics (01.05.2017)
Published in European journal of medical genetics (01.05.2017)
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Journal Article
Post-Traumatic Stress Disorder Following Cardiac Surgery: A Case Report of a Nine-Year-Old Female with Williams Syndrome
Alexander, Abigail J, Gallagher, Aidan, Pober, Barbara R, Waxler, Jessica L, McDougle, Christopher J
Published in Journal of intellectual & developmental disability (03.04.2019)
Published in Journal of intellectual & developmental disability (03.04.2019)
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Journal Article
Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
Mucha, Bettina E., Banka, Siddharth, Ajeawung, Norbert Fonya, Molidperee, Sirinart, Chen, Gary G., Koenig, Mary Kay, Adejumo, Rhamat B., Till, Marianne, Harbord, Michael, Perrier, Renee, Lemyre, Emmanuelle, Boucher, Renee-Myriam, Skotko, Brian G., Waxler, Jessica L., Thomas, Mary Ann, Hodge, Jennelle C., Gecz, Jozef, Nicholl, Jillian, McGregor, Lesley, Linden, Tobias, Sisodiya, Sanjay M., Sanlaville, Damien, Cheung, Sau W., Ernst, Carl, Campeau, Philippe M.
Published in Genetics in medicine (01.09.2019)
Published in Genetics in medicine (01.09.2019)
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Impact of literacy and numeracy on motivation for behavior change after diabetes genetic risk testing
Vassy, Jason L, O'Brien, Kelsey E, Waxler, Jessica L, Park, Elyse R, Delahanty, Linda M, Florez, Jose C, Meigs, James B, Grant, Richard W
Published in Medical decision making (01.07.2012)
Published in Medical decision making (01.07.2012)
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Skin findings in Williams syndrome
Kozel, Beth A., Bayliss, Susan J., Berk, David R., Waxler, Jessica L., Knutsen, Russell H., Danback, Joshua R., Pober, Barbara R.
Published in American journal of medical genetics. Part A (01.09.2014)
Published in American journal of medical genetics. Part A (01.09.2014)
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Journal Article
Genetic Counseling as a Tool for Type 2 Diabetes Prevention: A Genetic Counseling Framework for Common Polygenetic Disorders
Waxler, Jessica L., O’Brien, Kelsey E., Delahanty, Linda M., Meigs, James B., Florez, Jose C., Park, Elyse R., Pober, Barbara R., Grant, Richard W.
Published in Journal of genetic counseling (01.10.2012)
Published in Journal of genetic counseling (01.10.2012)
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Journal Article
Personalized Genetic Risk Counseling to Motivate Diabetes Prevention
Grant, Richard W., O’Brien, Kelsey E., Waxler, Jessica L., Vassy, Jason L., Delahanty, Linda M., Bissett, Laurie G., Green, Robert C., Stember, Katherine G., Guiducci, Candace, Park, Elyse R., Florez, Jose C., Meigs, James B.
Published in Diabetes care (01.01.2013)
Published in Diabetes care (01.01.2013)
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Journal Article
Design of a randomized trial of diabetes genetic risk testing to motivate behavior change: The Genetic Counseling/Lifestyle Change (GC/LC) Study for Diabetes Prevention
Grant, Richard W, Meigs, James B, Florez, Jose C, Park, Elyse R, Green, Robert C, Waxler, Jessica L, Delahanty, Linda M, O’Brien, Kelsey E
Published in Clinical trials (London, England) (01.10.2011)
Published in Clinical trials (London, England) (01.10.2011)
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Journal Article
Mutations in the evolutionarily highly conserved KEOPS complex genes cause nephrotic syndrome with microcephaly
Braun, Daniela A., Rao, Jia, Mollet, Geraldine, Schapiro, David, Daugeron, Marie-Claire, Tan, Weizhen, Gribouval, Olivier, Boyer, Olivia, Revy, Patrick, Jobst-Schwan, Tilman, Schmidt, Johanna Magdalena, Lawson, Jennifer A., Schanze, Denny, Ashraf, Shazia, Boddaert, Nathalie, Collinet, Bruno, Martin, Gaëlle, Liger, Dominique, Lovric, Svjetlana, Furlano, Monica, Guerrera, I. Chiara, Sanchez-Ferras, Oraly, Menten, Björn, Vergult, Sarah, De Rocker, Nina, Airik, Merlin, Hermle, Tobias, Shril, Shirlee, Widmeier, Eugen, Gee, Heon Yung, Choi, Won-Il, Sadowski, Carolin E., Pabst, Werner L., Warejko, Jillian, Daga, Ankana, LeBerre, Tamara Basta, Matejas, Verena, Behnam, Babak, Beeson, Brendan, Begtrup, Amber, Bruce, Malcolm, Ch'ng, Gaik-Siew, Lin, Shuan-Pei, Chang, Jui-Hsing, Chen, Chao-Huei, Cho, Megan T., Gipson, Patrick E., Hsu, Chyong-Hsin, Kari, Jameela A., Ke, Yu-Yuan, Kiraly-Borri, Cathy, Lai, Wai-ming, Lemyre, Emmanuelle, Littlejohn, Rebecca Okasha, Masri, Amira, Moghtaderi, Mastaneh, Nakamura, Kazuyuki, Praet, Marleen, Prasad, Chitra, Prytula, Agnieszka, Roeder, Elizabeth, Rump, Patrick, Schnur, Rhonda E., Shiihara, Takashi, Sinha, Manish, Soliman, Neveen A, Soulami, Kenza, Sweetser, David A., Tsai, Wen-Hui, Tsai, Jeng-Daw, Vester, Udo, Viskochil, David H., Vatanavicharn, Nithiwat, Waxler, Jessica L., Wolf, Matthias T.F., Wong, Sik-Nin, Poduri, Annapurna, Truglio, Gessica, Mane, Shrikant, Lifton, Richard P., Bouchard, Maxime, Kannu, Peter, Chitayat, David, Magen, Daniella, Calleweart, Bert, van Tilbeurgh, Herman, Zenker, Martin, Antignac, Corinne, Hildebrandt, Friedhelm
Published in Nature genetics (14.08.2017)
Published in Nature genetics (14.08.2017)
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