| Commensal Bacteroides species induce colitis in host-genotype-specific fashion in a mouse model of inflammatory bowel disease SM Bloom, VN Bijanki, GM Nava, L Sun, NP Malvin, DL Donermeyer, ... Cell host & microbe 9 (5), 390-403, 2011 | 517 | 2011 |
| Raine Syndrome (OMIM #259775), Caused By FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660) MP Whyte, WH McAlister, MD Fallon, ME Pierpont, VN Bijanki, S Duan, ... Journal of Bone and Mineral Research 32 (4), 757-769, 2017 | 49 | 2017 |
| New explanation for autosomal dominant high bone mass: mutation of low-density lipoprotein receptor-related protein 6 MP Whyte, WH McAlister, F Zhang, VN Bijanki, A Nenninger, ... Bone 127, 228-243, 2019 | 41 | 2019 |
| Melorheostosis: exome sequencing of an associated dermatosis implicates postzygotic mosaicism of mutated KRAS MP Whyte, M Griffith, L Trani, S Mumm, GS Gottesman, WH McAlister, ... Bone 101, 145-155, 2017 | 35 | 2017 |
| Non-endemic skeletal fluorosis: causes and associated secondary hyperparathyroidism (case report and literature review) FJ Cook, M Seagrove-Guffey, S Mumm, DJ Veis, WH McAlister, VN Bijanki, ... Bone 145, 115839, 2021 | 22 | 2021 |
| Lenz‐Majewski Hyperostotic Dwarfism with Hyperphosphoserinuria from a Novel Mutation in PTDSS1 Encoding Phosphatidylserine Synthase 1 MP Whyte, A Blythe, WH McAlister, AR Nenninger, VN Bijanki, S Mumm Journal of Bone and Mineral Research 30 (4), 606-614, 2015 | 22 | 2015 |
| Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation S Mumm, GS Gottesman, D Wenkert, PM Campeau, A Nenninger, ... Bone 130, 115047, 2020 | 21 | 2020 |
| Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review MP Whyte, SD Amalnath, WH McAlister, R Pedapati, V Muthupillai, ... Bone 116, 321-332, 2018 | 19 | 2018 |
| Healing of vitamin D deficiency rickets complicating hypophosphatasia suggests a role beyond circulating mineral sufficiency for vitamin D in musculoskeletal health EL Lin, GS Gottesman, WH McAlister, VN Bijanki, KE Mack, DM Griffin, ... Bone 136, 115322, 2020 | 17 | 2020 |
| ATRAID regulates the action of nitrogen-containing bisphosphonates on bone LE Surface, DT Burrow, J Li, J Park, S Kumar, C Lyu, N Song, Z Yu, ... Science translational medicine 12 (544), eaav9166, 2020 | 16 | 2020 |
| Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding … MP Whyte, SD Amalnath, WH McAlister, MD McKee, DJ Veis, M Huskey, ... Bone 132, 115190, 2020 | 15 | 2020 |
| Juvenile Paget's disease from heterozygous mutation of SP7 encoding Osterix (specificity protein 7, transcription factor SP7) MP Whyte, PM Campeau, WH McAlister, GD Roodman, N Kurihara, ... Bone 137, 115364, 2020 | 13 | 2020 |
| Hypophosphatasia: Vitamin B6 status of affected children and adults MP Whyte, F Zhang, D Wenkert, KE Mack, VN Bijanki, KL Ericson, ... Bone 154, 116204, 2022 | 10 | 2022 |
| Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25‐Dihydroxyvitamin D‐Mediated Hypercalcemia and Generalized Osteosclerosis MP Whyte, E Lim, WH McAlister, GS Gottesman, L Trinh, DJ Veis, ... Journal of Bone and Mineral Research 33 (11), 2071-2080, 2018 | 10 | 2018 |
| PM Allen, TS Stappenbeck, Commensal Bacteroides species induce colitis in host-genotype-specific fashion in a mouse model of inflammatory bowel disease SM Bloom, VN Bijanki, GM Nava, L Sun, NP Malvin, DL Donermeyer, ... Cell Host Microbe 9, 390-403, 2011 | 8 | 2011 |
| X-Linked Hypophosphatemia: All Eight Individuals Representing Separate American Families Carrying the PHEX 3'UTR Mutation c.* 231A> G Tested Positive for an Exon 13-15 Duplication S Mumm, M Huskey, S Duan, V Wollberg, V Bijanki, GS Gottesman, ... Journal of Bone and Mineral Research 34, 170-170, 2019 | 7 | 2019 |
| Coalescing expansile skeletal disease: delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V MP Whyte, J Aronson, WH McAlister, RS Weinstein, D Wenkert, ... Bone 145, 115835, 2021 | 6 | 2021 |
| Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy MP Whyte, NS Ma, S Mumm, GS Gottesman, WH McAlister, AR Nenninger, ... Bone 138, 115459, 2020 | 5 | 2020 |
| LRP6 mutation: a new cause of autosomal dominant high bone mass MP Whyte, GS Gottesman, EL Lin, WH Mcalister, A Nenninger, VN Bijanki, ... JOURNAL OF BONE AND MINERAL RESEARCH 33, 57-57, 2018 | 4 | 2018 |
| ATRAID, a genetic factor that regulates the action of nitrogen-containing bisphosphonates on bone LE Surface, DT Burrow, J Li, J Park, S Kumar, C Lyu, N Song, Z Yu, ... bioRxiv, 338350, 2018 | 3 | 2018 |
