Physician
Pediatrics
Dr. Patricia I. Bader, MD
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Patricia Bader works in the field of Pediatrics. He went to Indiana University School of Medicine. Indiana University School of Medicine is ranked 45 in research and 47 in primary care medicine He received awards:"Fellow (FAAP)". Doctor Patricia I. Bader, MD is a published doctor. He has 53 papers published. The most current publication "A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes." He is registered with Medicare.
Publications
- Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene.
- Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.
- CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree.
- TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities.
- Investigation of NRXN1 deletions: Clinical and molecular characterization.
- High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with ...
- A de novo deletion of CALN1 in a male with a bilateral diaphragmatic defect does not definitely cause this malformation.
- Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems.
- Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity.
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
- New perspectives on the face in fetal alcohol syndrome: what anthropometry tells us.
- Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesis.
- Facial dysmorphology, roentgenographic measurements, and clinical genetics.
- A prospective analysis of the pattern of immune reconstitution in a paediatric cohort following transplantation of positively selected human leucocyte antigen-disparat...
- A prospective comparison of immune reconstitution in pediatric recipients of positively selected CD34+ peripheral blood stem cells from unrelated donors vs recipients ...
- Multivariate analyses of immune reconstitution in children after allo-SCT: risk-estimation based on age-matched leukocyte sub-populations.
- Characterization of lineage-specific chimaerism in patients with acute leukaemia and myelodysplastic syndrome after allogeneic stem cell transplantation before and aft...
- Mixed hematopoietic chimerism after allogeneic bone marrow transplantation: the impact of quantitative PCR analysis for prediction of relapse and graft rejection in ch...
- Adenoviral infections after transplantation of positive selected stem cells from haploidentical donors in children: an update.
- A comparison between three graft manipulation methods for haploidentical stem cell transplantation in pediatric patients: preliminary results of a pilot study.
- Enrichment of cell subpopulations applying automated MACS technique: purity, recovery and applicability for PCR-based chimerism analysis.
- Quantification of chimerism within peripheral blood, bone marrow and purified leukocyte subsets: comparison of singleplex and multiplex PCR amplification of short tand...
- Risk factors for treatment failures in patients receiving PCR-based preemptive therapy for CMV infection.
- Deletion of Huntington''s disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.
- Toward quality assurance for metaphase FISH: a multi-center experience.
- Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolate.
- Infantile refsum disease in four Amish sibs.
- Toward quality assurance for metaphase FISH: a multicenter experience.
- Immunoglobulin and T-cell receptor gene rearrangements as PCR-based targets are stable markers for monitoring minimal residual disease in acute lymphoblastic leukemia ...
- Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study.
- Minimal residual disease (MRD) status prior to allogeneic stem cell transplantation is a powerful predictor for post-transplant outcome in children with ALL.
- Vitiligo and dysgammaglobulinemia. A case report and family study.
- Inheritance of idiopathic nephrotic syndrome.
- Familial nephrotic syndrome.
- The effect of mandibular position on appendage muscle strength.
- Increasing mixed chimerism defines a high-risk group of childhood acute myelogenous leukemia patients after allogeneic stem cell transplantation where pre-emptive immu...
- Brief clinical report: neural tube defects in dup(11q).
- A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes.
- Partial deletion of chromosome 6p: delineation of the syndrome.
- Parent to child transmission of the thrombocytopenia absent radius (TAR) syndrome.
- Brief clinical report: two children with de novo del(9p).
- Identification of critical regions for clinical features of distal 10q deletion syndrome.
- The subtle facial signs of prenatal exposure to alcohol: an anthropometric approach.
- 22q13.3 deletion syndrome: clinical and molecular analysis using array CGH.
- PTCH1 duplication in a family with microcephaly and mild developmental delay.
- A copy number variation morbidity map of developmental delay.
- Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions.
- Mixed gonadal dysgenesis in a child with isodicentric Y chromosome: Does the relative proportion of the 45,X line really matter?
- Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay.
- Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia.
- Phenotypic manifestations of copy number variation in chromosome 16p13.11.
- MECP2 duplications in six patients with complex sex chromosome rearrangements.
Schools
Indiana University School Of Medicine
Indiana University School Of Med
Doctors Specialties
- Clinical Cytogenetics
- Clinical Genetics
- Pediatrics
Accepted Insurances
- Choice Plus POS II
- Anthem Blue Cross Blue Shield PPO
- Blue Card PPO
- Blue Cross Blue Shield of Illinois PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- First Health (Coventry Health Care) PPO
- Frontpath Health Coalition
- Choice Care PPO
- Medicaid
- Medicare MCR
- Sagamore Plus
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Awards
- Fellow (FAAP)
Education
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Indiana University School of Medicine
Drug Facts
| NPI NUMBER | 1841478336 | |
| NPPES Provider LastName | BADER | |
| NPPES Provider FirstName | PATRICIA | |
| NPPES Provider ZIPCode | 468451727 | |
| NPPES Provider State | IN | |
| Specialty Description | Pediatric Medicine | |
| Total Claim Count | 126.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1841478336 |
| Last Name Of The Provider | BADER |
| First Name Of The Provider | PATRICIA |
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