Laxmi Ghimire

Rongkavilit Chokechai

 Krishna Siruguppa

David Yi

Abu-Shamsieh, A; Maw, S. Pediatric Care for Immigrant, Refugee, and Internationally Adopted Children. 2022 Feb; 69(1) DOI

Wang, JY; Foroutan, A; Richardson, E; Skinner, SA; Reilly, J; Kerkhof, J; Curry, CJ; Tarpey, PS; Robertson, SP; Maystadt, I; Keren, B; Dixon, JW; Skinner, C; Stapleton, R; Ruaud, L; Gumus, E; Lakeman, P; Alders, M; Tedder, ML; Schwartz, CE; Friez, MJ; Sadikovic, B; Stevenson, RE. Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711. 2022, Apr; 30(4)

Kumble, S; Levy, AM; Garcia-Minaur, S; Gao, H; Palomares-Bralo, M; Pacio-Miguez, M; Parikh, S; Ritter, AL; Izumi, K; Hoffman, TL; Oppermann, H; Bjerglund, L; Rosenfeld, JA; Curry, C; Faivre, L; Leiber, A; Robinson, S; Finkel, RS; Gerard, A; Cohen, JS; Xie, Y; Mullegama, SV; Platzer, K; Sacoto, MJG; Revah-Politi, A; Berger, SM; Comi, AM; Anyane-Yeboa, K; Fievet, A; Mintz, CS; Lozano, R; Posey, JE; Ciliberto, M; Howard, L; Benke, P; Odent, S; Denomme-Pichon, AS; Weber, M; Mew, NA; Ostergaard, E; Iglesias, AD; Punetha, J; Chung, WK; Brown, N; Tumer, Z. Expanding the phenotype of QRICH1 associated neurodevelopmental disorder. 2022, Apr; 30(1)

Kumble, S; Levy, AM; Punetha, J; Gao, H; Mew, NA; Anyane-Yeboa, K; Benke, PJ; Berger, SM; Bjerglund, L; Campos-Xavier, B; Ciliberto, M; Cohen, JS; Comi, AM; Curry, C; Damaj, L; Denomme-Pichon, AS; Emrick, L; Faivre, L; Fasano, MB; Fievet, A; Finkel, RS; Garcia-Minaur, S; Gerard, A; Gomez-Puertas, P; Sacoto, MGJ; Hoffman, TL; Howard, L; Iglesias, AD; Izumi, K; Larson, A; Leiber, A; Lozano, R; Marcos-Alcalde, I; Mintz, CS; Mullegama, SV; Moller, RS; Odent, S; Oppermann, H; Ostergaard, E; Pacio-Miguez, M; Palomares-Bralo, M; Parikh, S; Paulson, AM; Platzer, K; Posey, JE; Potocki, L; Revah-Politi, A; Rio, M; Ritter, AL; Robinson, S; Rosenfeld, JA; Santos-Simarro, F; Sousa, SB; Weber, M; Xie, YL; Chung, WK; Brown, NJ; Tumer, Z. The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder. 2022, Feb; 43(2)

Naeem, F; Rongkavilit, C. Exotic Infections Are Only One Plane Away Preface. 2022 Feb; 69(1)

MacDonell, KK; Wang, B; Phanuphak, N; Janamnuaysook, R; Srimanus, P; Rongkavilit, C; Naar, S. Optimizing an mHealth Intervention to Improve Uptake and Adherence to HIV Pre-exposure Prophylaxis in Young Transgender Women: Protocol for a Multi-Phase Trial. 2022, May; 11(5)

Thilakaratne, R; Graham, S; Moua, J; Jones, CG; Collins, C; Mann, J; Sciortino, S; Wong, J; Kharrazi, M. CFTR gene variants, air pollution, and childhood asthma in a California Medicaid population. 2022, Nov; 57(11)

Bunnalai, T; Fontenette, R; Siruguppa, K; Vargas, V; Neville, C; Waugh, J; Merriman, M; Lien, T; Covarrubias, L; Ip, A; Husted, H. IMPLEMENTATION OF A COLLABORATIVE PEDIATRIC AND ADULT HYBRID TEAM IN THE CARE OF CRITICALLY ILL ADULT PATIENTS DURING CORONAVIRUS PANDEMIC: AN EXPERIENCE FROM A LARGE COMMUNITY HOSPITAL IN SAN JOAQUIN VALLEY, CALIFORNIA. 2021, Jan; 69(1)

Lemire, G; Ito, YA; Marshall, AE; Chrestian, N; Stanley, V; Brady, L; Tarnopolsky, M; Curry, CJ; Hartley, T; Mears, W; Derksen, A; Rioux, N; Laflamme, N; Hutchison, HT; Pais, LS; Zaki, MS; Sultan, T; Dane, AD; Gleeson, JG; Vaz, FM; Kernohan, KD; Bernard, G; Boycott, KM. ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies. 2021, Oct; 108(10)

Park, KB; Chapman, T; Aldinger, KA; Mirzaa, GM; Zeiger, J; Beck, A; Glass, IA; Hevner, RF; Jansen, AC; Marshall, DA; Oegema, R; Parrini, E; Saneto, RP; Curry, CJ; Hall, JG; Guerrini, R; Leventer, RJ; Dobyns, WB. The spectrum of brain malformations and disruptions in twins. 2021, Sep; 185(9)

Zarate, YA; Bosanko, KA; Thomas, MA; Miller, DT; Cusmano-Ozog, K; Martinez-Monseny, A; Curry, CJ; Graham, JM; Velsher, L; Bekheirnia, MR; Seidel, V; Dedousis, D; Mitchell, AL; DiMarino, AM; Riess, A; Balasubramanian, M; Fish, JL; Caffrey, AR; Fleischer, N; Pierson, TM; Lacro, RV. Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. 2021, Apr; 99(4).

Serpieri, V; D’Abrusco, F; Dempsey, JC; Cheng, YHH; Arrigoni, F; Baker, J; Battini, R; Bertini, ES; Borgatti, R; Christman, AK; Curry, C; D’Arrigo, S; Fluss, J; Freilinger, M; Gana, S; Ishak, GE; Leuzzi, V; Loucks, H; Manti, F; Mendelsohn, N; Merlini, L; Miller, CV; Muhammad, A; Nuovo, S; Romaniello, R; Schmidt, W; Signorini, S; Siliquini, S; Szczaluba, K; Vasco, G; Wilson, M; Zanni, G; Boltshauser, E; Doherty, D; Valente, EM. SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum. 2021, Oct;59(9)

Biesecker, LG; Adam, MP; Alkuraya, FS; Amemiya, AR; Bamshad, MJ; Beck, AE; Bennett, JT; Bird, LM; Carey, JC; Chung, B; Clark, RD; Cox, TC; Curry, C; Dinulos, MBP; Dobyns, WB; Giampietro, PF; Girisha, KM; Glass, IA; Graham, JM; Gripp, KW; Haldeman-Englert, CR; Hall, BD; Innes, AM; Kalish, JM; Keppler-Noreuil, KM; Kosaki, K; Kozel, BA; Mirzaa, GM; Mulvihill, JJ; Nowaczyk, MJM; Pagon, RA; Retterer, K; Rope, AF; Sanchez-Lara, PA; Seaver, LH; Shieh, JT; Slavotinek, AM; Sobering, AK; Stevens, CA; Stevenson, DA; Tan, TY; Tan, WH; Tsai, AC; Weaver, DD; Williams, MS; Zackai, E; Zarate, YA. A dyadic approach to the delineation of diagnostic entities in clinical genomics. 2021, Jan; 108(1)

Higa, LA; Wardley, J; Wardley, C; Singh, S; Foster, T; Shen, JJ. CNKSR2-related neurodevelopmental and epilepsy disorder: a cohort of 13 new families and literature review indicating a predominance of loss of function pathogenic variants. 2021, July; 14(1)

Galindo, R; Chow, H; Rongkavilit, C. COVID-19 in Children Clinical Manifestations and Pharmacologic Interventions Including Vaccine Trials. 2021 Oct; 68(5)

Bunnalai, T; Fontenette, R; Siruguppa, K; Vargas, V; Neville, C; Waugh, J; Merriman, M; Lien, T; Covarrubias, L; Ip, A; Husted, H. IMPLEMENTATION OF A COLLABORATIVE PEDIATRIC AND ADULT HYBRID TEAM IN THE CARE OF CRITICALLY ILL ADULT PATIENTS DURING CORONAVIRUS PANDEMIC: AN EXPERIENCE FROM A LARGE COMMUNITY HOSPITAL IN SAN JOAQUIN VALLEY, CALIFORNIA. 2021, Jan; 69(1)

Naeem, F; Vijayan, V; Kim, BY; Rahmati, E; McCarty, J. Congenital Coccidioidomycosis: A Case Report and Review of the Literature. 2021, July; 10(7)

Keles, ES. Mild SARS-CoV-2 infections in children might be based on evolutionary biology and linked with host reactive oxidative stress and antioxidant capabilities. 2020 Jan; 36

Adam, AP; Curry, CJ; Hall, JG; Keppler-Noreuil, KM; Adam, MP; Dobyns, WB. Recurrent constellations of embryonic malformations re-conceptualized as an overlapping group of disorders with shared pathogenesis. 2020, Nov; 182(11)

Macmillan, P; Frye, J; Bunnalai, T; Kaups, K. Crisis Standards of Care Guidelines for the COVID-19 Pandemic: Fresno Resource Allocation Guide (FRAG). 2020 Nov; 13(11)

A Teenager With Cough, Weight Loss, and a Chest Wall Mass. Clin Pediatr (Phila). 2020 05; 59(4-5):522-528. Marquez I, Hardee S, Kim S, Webb N, Roberto L, Sanchez-Glanville C, Rongkavilit C. PMID: 31965823 -> A Teenager With Cough, Weight Loss, and a Chest Wall Mass – PubMed (nih.gov)

Update on Coccidioidomycosis in the United States and Beyond. Global Pediatric Health. 2020; 7:2333794X20969282. Bajwa AK, Rongkavilit C. à Update on Coccidioidomycosis in the United States and Beyond – PubMed (nih.gov)

Please add this next publication under the 2021 tab: Mei Lan Chen, Xiangsheng Huang#, HongtaoWang*, et al. CAR directs T cell adaptation to bile acids in the small intestine. Nature. 2021 May; 593 (147-151). PubMed PMID: 33828301. à CAR directs T cell adaptation to bile acids in the small intestine – PMC (nih.gov)

• “Establishing guidelines for Pediatric Fever in a Community Hospital,” Allie Johnston, MD, Ramin Azhir, MD, Amreeta Panesar, MD. Mentors: Eric Schmitt, MD, MPH and Chokechai Rongkavilit, MD. Abstract 161, presented at Western Medical Research Conference, Carmel, 2020.
• “Improving resident confidence at neonatal resuscitation through increased exposure,” Ming Cai, MD. Mentor: Erica Gastelum, MD. Abstract 207, presented at Western Medical Research Conference, Carmel, 2020.

• “Patients with Genetic Variants of Unknown Significance for Primary Ciliary Dyskinesia: A Case Series,” Derek Corpus, MD, Mentors: John Moua, MD; Paul Do, MD. Abstract 401, presented at Western Medical Research Conference, Carmel, 2020.
• “Quality Improvement in The Outpatient Management of Pediatric Asthma in The Central Valley,” Kali Hockett, MD; Cindy Nguyen, DO; Derek Corpus, MD; Ozge Dogan, MD; Melissa Jasinto, MD; Veriah Vidales, MD; Mentors: Naomi Bardach, MD; Christian Faulkenberry-Miranda, MD. Abstract 232, presented at Western Medical Research Conference, Carmel, 2020.
• “Unusual Presentation of Acute Hepatitis Complicated by Pancreatitis in A Child,” Ozge Dogan, MD, Mentor: Michael Haight, MD. Abstract 436, presented at Western Medical Research Conference, Carmel, 2020.