SIPARADIGM LLC
NPI 1891909941
Clinical Medical Laboratory in Pine Brook, NJ

Areas of Expertise

The following services and procedures, recently provided to Medicare patients, illustrate the range of care this provider offers. This list reflects the variety of services available to all patients visiting the practice and is based on 2022 Medicare dataset. In general, the more frequently a provider treats specific conditions or performs particular procedures, the more experienced they become in addressing similar patient needs. The provider has delivered many of the services listed below to Medicare patients. Please note that this list does not include services provided to patients who are not covered by Medicare.

Bone marrow, smear interpretation

Bone marrow smear interpretation is a procedure where a small sample of your bone marrow is taken and examined under a microscope. This helps doctors identify any abnormal cells or signs of diseases such as anemia, leukemia, or infections. It's a crucial step in diagnosing various blood disorders.

This service was performed 129 times for 124 patients

Bone marrow, smear interpretation

Bone marrow smear interpretation is a procedure where a small sample of your bone marrow is taken and examined under a microscope. This helps doctors identify any abnormal cells or signs of diseases such as anemia, leukemia, or infections. It's a crucial step in diagnosing various blood disorders.

This service was performed 789 times for 752 patients

Cell examination of specimen, selective cellular enhancement technique

Cell examination of a specimen using selective cellular enhancement technique is a lab process that improves the visibility of certain cells in a sample. It helps in identifying abnormalities or diseases. The process is non-invasive, safe, and aids in accurate diagnosis.

This service was performed 118 times for 116 patients

Cell examination of specimen, selective cellular enhancement technique

Cell examination of a specimen using selective cellular enhancement technique is a lab process that improves the visibility of certain cells in a sample. It helps in identifying abnormalities or diseases. The process is non-invasive, safe, and aids in accurate diagnosis.

This service was performed 472 times for 454 patients

Chromosome analysis for genetic defects, additional karyotypes, each study

Chromosome analysis is a test that examines the number and structure of a person's chromosomes. This is done to identify any genetic defects. Additional karyotypes, each study, are further tests that look at the arrangement of these chromosomes. This can help in detecting genetic disorders.

This service was performed 24 times for 24 patients

Chromosome analysis for genetic defects, analyze 20-25 cells

Chromosome analysis is a test that evaluates your cells to check for genetic defects. In this procedure, 20-25 cells are examined under a microscope to identify any abnormalities. This information can help in diagnosing certain genetic conditions and guide treatment plans.

This service was performed 1,026 times for 993 patients

Chromosome analysis for genetic defects, count 15-20 cells

Chromosome analysis is a test that examines your body's cell structure to detect any genetic abnormalities. In this procedure, 15-20 cells are studied to identify any unusual changes that may indicate a genetic disorder. This helps in early detection and management of potential health issues.

This service was performed 19 times for 19 patients

Complete blood cell count (red cells, white blood cell, platelets), automated test and automated differential white blood cell count

A Complete Blood Cell Count is a common test that measures various components of the blood, including red cells (carry oxygen), white cells (fight infection), and platelets (help blood clot). An automated test ensures accuracy. The differential count provides detailed information about white cell types.

This service was performed 258 times for 253 patients

Flow cytometry technique for dna or cell analysis, 16 or more markers

Flow cytometry is a method used to measure and analyze cells. It uses a beam of light to detect up to 16 or more markers on cells, helping to identify their type, function, or abnormalities. This technique aids in diagnosing various health conditions.

This service was performed 461 times for 426 patients

Flow cytometry technique for dna or cell analysis, 16 or more markers

Flow cytometry is a method used to measure and analyze cells. It uses a beam of light to detect up to 16 or more markers on cells, helping to identify their type, function, or abnormalities. This technique aids in diagnosing various health conditions.

This service was performed 1,904 times for 1,795 patients

Flow cytometry technique for dna or cell analysis, 2 to 8 markers

Flow cytometry is a technique that helps analyze your cells and DNA. It uses lasers to identify and sort cells based on their properties, marked by up to 8 different markers. This helps in diagnosing and monitoring various health conditions.

This service was performed 17 times for 17 patients

Flow cytometry technique for dna or cell analysis, 9 to 15 markers

Flow cytometry is a technique used to measure physical and chemical characteristics of cells or particles. It can analyze multiple markers (9 to 15) on a cell, helping to identify its type and function. This process can also examine DNA within cells for any abnormalities.

This service was performed 39 times for 39 patients

Flow cytometry technique for dna or cell analysis, 9 to 15 markers

Flow cytometry is a technique used to measure physical and chemical characteristics of cells or particles. It can analyze multiple markers (9 to 15) on a cell, helping to identify its type and function. This process can also examine DNA within cells for any abnormalities.

This service was performed 361 times for 355 patients

Flow cytometry technique for dna or cell analysis, each additional marker

Flow cytometry is a technique that helps analyze the physical and chemical characteristics of cells or particles. When an additional marker is used, it aids in identifying specific cell types or stages of disease. This helps in precise diagnosis and treatment planning.

This service was performed 42,321 times for 1,870 patients

Flow cytometry technique for dna or cell analysis, first marker

Flow cytometry is a technique used to examine microscopic particles, like cells or DNA. It employs a beam of light to detect and measure physical and chemical characteristics of these particles. The 'first marker' refers to a specific characteristic or feature used to identify a particular cell or particle.

This service was performed 1,989 times for 1,872 patients

Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase)

Gene analysis of the ABL1 gene helps identify changes that may cause certain health issues. It involves examining the ABL1 gene, which makes a protein involved in cell division and communication. This test aids in diagnosing and managing treatment for these conditions.

This service was performed 17 times for 14 patients

Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants

Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.

This service was performed 37 times for 37 patients

Gene analysis (calreticulin), common variants

Gene analysis of calreticulin, common variants, is a test that looks at specific genes to identify changes that may cause certain health issues. It helps in understanding your genetic makeup and potential health risks. It's a simple procedure involving a blood or saliva sample.

This service was performed 41 times for 41 patients

Gene analysis (epidermal growth factor receptor), common variants

Gene analysis of the epidermal growth factor receptor (EGFR) identifies common variants in this particular gene. This test helps in understanding your body's response to certain medications. It aids in personalized treatment planning, ensuring the most effective care.

This service was performed 11 times for 11 patients

Gene analysis (janus kinase 2) targeted sequence analysis

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

This service was performed 189 times for 189 patients

Gene analysis (janus kinase 2) variant

Gene analysis (Janus Kinase 2 variant) is a test that examines your DNA to identify any changes in the JAK2 gene. This gene is crucial for blood cell production. If it's mutated, it can lead to various blood disorders. The test helps in diagnosing these conditions.

This service was performed 131 times for 130 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) for detection of common variants

Gene analysis for the MPL proto-oncogene, thrombopoietin receptor, is a test that looks for common genetic variants. This helps in understanding certain health conditions related to blood cell production. It's a non-invasive procedure, involving a simple blood draw.

This service was performed 166 times for 166 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis

Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.

This service was performed 17 times for 17 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis

Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.

This service was performed 19 times for 19 patients

Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant

Gene analysis for the p.Leu265Pro variant involves studying the MYD88 gene, which plays a crucial role in immune response. This test helps identify changes in this gene that could potentially cause health issues. It's a non-invasive procedure, done through a blood sample.

This service was performed 42 times for 41 patients

Gene analysis (partner and localizer of brca2) full sequence analysis

Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.

This service was performed 35 times for 35 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis

Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.

This service was performed 19 times for 19 patients

Gene analysis (v-raf murine sarcoma viral oncogene homolog b1)

Gene analysis of v-raf murine sarcoma viral oncogene homolog b1 (BRAF) is a test that examines your DNA to identify changes or mutations in the BRAF gene. This information can help in diagnosing and treating certain diseases, including some types of cancer.

This service was performed 30 times for 30 patients

Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis

Gene rearrangement analysis is a test that studies alterations in your immune system's DNA. Specifically, it evaluates the variable region somatic mutation in the immunoglobulin heavy chain locus, which helps understand your body's immune response.

This service was performed 230 times for 228 patients

Genetic sequencing localization, initial procedure

Genetic sequencing localization is a process to identify where specific genes are located in your DNA. During the initial procedure, a sample of your cells is collected, usually through a simple swab or blood test. This data is then analyzed to pinpoint the location of certain genes. This can help understand your genetic makeup and potential health risks.

This service was performed 19 times for 19 patients

Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, cdc or non-cdc, making use of high throughput technologies, completed within

This is a test to detect the COVID-19 virus. It uses a technique that amplifies the virus's genetic material (DNA or RNA) for detection. High throughput technologies are used for rapid and large-scale testing. The procedure is completed within a set time frame.

This service was performed 2,302 times for 863 patients

Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, making use of high throughput technologies as described by cms-2020-01-r

This is a test for COVID-19. It uses high-tech methods to find the virus's genetic material in your body. The amplified probe technique helps detect the virus even in small amounts. This is crucial for early detection and effective treatment.

This service was performed 2,405 times for 873 patients

Interpretation and report of genetic testing

Interpretation and report of genetic testing involves analyzing your DNA to look for changes that could indicate a risk for certain health conditions. The results are then compiled into a report, which provides insights about your genetic health.

This service was performed 195 times for 183 patients

Interpretation and report of genetic testing

Interpretation and report of genetic testing involves analyzing your DNA to look for changes that could indicate a risk for certain health conditions. The results are then compiled into a report, which provides insights about your genetic health.

This service was performed 1,056 times for 1,018 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure

Microscopic genetic analysis of tissue is a detailed lab process that examines your cells' genetic material. If more than one stain procedure is needed, it's termed an 'additional multiplex stain procedure'. This helps to highlight different components within your cells, aiding in accurate diagnosis and treatment planning.

This service was performed 1,308 times for 382 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure

Microscopic genetic analysis of tissue is a detailed lab process that examines your cells' genetic material. If more than one stain procedure is needed, it's termed an 'additional multiplex stain procedure'. This helps to highlight different components within your cells, aiding in accurate diagnosis and treatment planning.

This service was performed 5,817 times for 1,721 patients

Microscopic genetic analysis of tissue, manual, each additional procedure

Microscopic genetic analysis of tissue is a procedure where a small sample of your body tissue is examined under a microscope. This is done to study the genes in your cells. If more than one procedure is needed, each additional one involves repeating this process. It's a key part of diagnosing and managing many health conditions.

This service was performed 91 times for 84 patients

Microscopic genetic analysis of tissue, manual, initial procedure

Microscopic genetic analysis of tissue is a test that examines your cells under a microscope. This helps to identify any genetic changes that could be causing health issues. It's the first step in a series of tests to pinpoint the root cause of your symptoms.

This service was performed 199 times for 193 patients

Microscopic genetic analysis of tissue, manual, initial procedure

Microscopic genetic analysis of tissue is a test that examines your cells under a microscope. This helps to identify any genetic changes that could be causing health issues. It's the first step in a series of tests to pinpoint the root cause of your symptoms.

This service was performed 878 times for 846 patients

Microscopic genetic analysis of tumor, manual

Microscopic genetic analysis of a tumor involves examining your tumor's genes under a microscope. This helps identify specific genetic changes in the tumor cells. This information can aid in diagnosing, predicting disease progression, and determining the most effective treatment options.

This service was performed 84 times for 80 patients

Microscopic genetic analysis of tumor, manual

Microscopic genetic analysis of a tumor involves examining your tumor's genes under a microscope. This helps identify specific genetic changes in the tumor cells. This information can aid in diagnosing, predicting disease progression, and determining the most effective treatment options.

This service was performed 357 times for 319 patients

Molecular pathology procedure; physician interpretation and report

A molecular pathology procedure involves analyzing your body's cells at a molecular level to identify any abnormalities. This can help detect diseases early. A physician will interpret the results and provide a detailed report, explaining the findings clearly.

This service was performed 2,976 times for 2,725 patients

Pathology examination of tissue using a microscope, intermediate complexity

A pathology examination of tissue with intermediate complexity involves studying a small sample of your body tissue under a microscope. This helps in identifying any abnormal cells or signs of disease. It's a detailed process requiring expert analysis to ensure accurate results.

This service was performed 227 times for 126 patients

Pathology examination of tissue using a microscope, intermediate complexity

A pathology examination of tissue with intermediate complexity involves studying a small sample of your body tissue under a microscope. This helps in identifying any abnormal cells or signs of disease. It's a detailed process requiring expert analysis to ensure accurate results.

This service was performed 1,378 times for 781 patients

Preparation of specimen, manual

The preparation of a specimen manually is a procedure where a sample from your body is collected by a healthcare professional. This could be blood, urine, or tissue. The sample is then prepared in a lab for further analysis to help diagnose or monitor your health condition.

This service was performed 93 times for 92 patients

Preparation of specimen, manual

The preparation of a specimen manually is a procedure where a sample from your body is collected by a healthcare professional. This could be blood, urine, or tissue. The sample is then prepared in a lab for further analysis to help diagnose or monitor your health condition.

This service was performed 361 times for 356 patients

Preparation of tissue for examination by removing any calcium present

This procedure involves treating tissue samples to remove any calcium, which can interfere with the examination. The tissue is soaked in a special solution that safely dissolves the calcium, leaving the tissue intact for accurate analysis. This helps in making precise diagnoses.

This service was performed 127 times for 122 patients

Preparation of tissue for examination by removing any calcium present

This procedure involves treating tissue samples to remove any calcium, which can interfere with the examination. The tissue is soaked in a special solution that safely dissolves the calcium, leaving the tissue intact for accurate analysis. This helps in making precise diagnoses.

This service was performed 794 times for 756 patients

Special stained specimen slides to examine tissue including interpretation and report

Special stained specimen slides are used to examine tissue samples. This involves applying special dyes to the tissue, which helps to highlight certain features under a microscope. The findings are then interpreted and a report is provided. This can aid in diagnosing various health conditions.

This service was performed 536 times for 125 patients

Special stained specimen slides to examine tissue including interpretation and report

Special stained specimen slides are used to examine tissue samples. This involves applying special dyes to the tissue, which helps to highlight certain features under a microscope. The findings are then interpreted and a report is provided. This can aid in diagnosing various health conditions.

This service was performed 3,303 times for 765 patients

Special stained specimen slides to examine tissue, each additional procedure

Special stained specimen slides are used to analyze tissue in detail. In this process, extra procedures may be needed for a more thorough examination. These involve applying special stains to the tissue on slides, enhancing specific elements for closer study.

This service was performed 717 times for 158 patients

Special stained specimen slides to examine tissue, each additional procedure

Special stained specimen slides are used to analyze tissue in detail. In this process, extra procedures may be needed for a more thorough examination. These involve applying special stains to the tissue on slides, enhancing specific elements for closer study.

This service was performed 4,419 times for 927 patients

Special stained specimen slides to examine tissue, initial procedure

This procedure involves the use of specially stained slides to examine tissue samples. The initial process involves obtaining a small tissue sample from your body. This sample is then placed on a slide and stained with special dyes to highlight different structures and elements. The stained slide is then examined under a microscope to help diagnose any potential health issues.

This service was performed 184 times for 175 patients

Special stained specimen slides to examine tissue, initial procedure

This procedure involves the use of specially stained slides to examine tissue samples. The initial process involves obtaining a small tissue sample from your body. This sample is then placed on a slide and stained with special dyes to highlight different structures and elements. The stained slide is then examined under a microscope to help diagnose any potential health issues.

This service was performed 1,015 times for 963 patients

Specimen collection for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]) from an individual in a snf or by a laboratory on behalf of a hha, any specimen source

Specimen collection for SARS-CoV-2 (COVID-19) involves taking a sample, typically from your nose or throat, using a swab. This sample is then sent to a lab for testing. The process is quick and relatively painless, helping to identify if you have the virus.

This service was performed 71 times for 71 patients

Specimen collection for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), any specimen source

Specimen collection for SARS-CoV-2, the virus causing COVID-19, involves taking a sample from the nose or throat using a swab. This sample is then analyzed in a lab to detect the presence of the virus. It's a crucial step in diagnosing COVID-19.

This service was performed 820 times for 454 patients

Surgical pathology consultation and report on referred material requiring preparation of slides

A surgical pathology consultation involves the examination of tissue removed during surgery. The tissue is processed and slides are prepared for detailed study under a microscope. The findings are then compiled into a report to help guide your treatment plan.

This service was performed 13 times for 12 patients

Targeted genomic sequence analysis panel of dna or combine dna and rna of 51 or greater genes associated with blood and lymphatic system disorders

A genetic test for cancer is a medical test that checks your DNA for changes or mutations that might put you at risk for cancer. It's a proactive step to understand your health better and possibly take preventive measures if needed.

This service was performed 1,510 times for 1,461 patients

Targeted genomic sequence analysis panel of dna or combine dna and rna of 5-50 genes associated with blood and lymphatic system disorders

This test examines your DNA to identify any genetic changes that could indicate a risk for blood-related cancers. It's a simple process where a sample of your blood or saliva is taken and sent to a lab for detailed examination.

This service was performed 227 times for 225 patients

Targeted genomic sequence analysis panel of dna or combined dna and rna of 5-50 genes associated with solid organ neoplasm

This test identifies specific genes linked with body organ cancer. It's a simple process where a sample of your blood or saliva is collected. The sample is then analyzed in a lab to find any genetic changes that might increase cancer risk. It's a proactive step to manage your health.

This service was performed 205 times for 205 patients

Tissue culture for tumor disorders of bone marrow and blood cells

Tissue culture for tumor disorders of bone marrow and blood cells is a lab process where your cells are grown in a controlled environment. The aim is to detect and study abnormal cells, such as cancer, in your bone marrow or blood. This helps in planning effective treatment.

This service was performed 1,092 times for 1,053 patients

Translocation analysis (bcr/abl1) major breakpoint

Translocation analysis (bcr/abl1) major breakpoint is a test that checks for a specific gene rearrangement in your cells. This rearrangement is often seen in certain types of leukemia. The test helps doctors diagnose and monitor treatment for these conditions.

This service was performed 338 times for 186 patients

Translocation analysis (bcr/abl1) minor breakpoint

Translocation analysis (bcr/abl1) minor breakpoint is a genetic test that identifies specific changes in chromosomes. It's used to diagnose certain types of blood cancers. The test detects rearrangements of genetic material, aiding in the treatment plan.

This service was performed 79 times for 61 patients

CLIA Information

The Clinical Laboratory Improvement Amendments (CLIA) of 1988 applies to facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease. The CLIA Program sets standards for clinical laboratory testing and issues certificates. The NPI / CLIA crosswalk information for this NPI number is:

CLIA Number

31D1028659

Facility Type

Independent

Certificate Effective Date

March 21, 2025

Certificate Expiration Date

March 20, 2027

Laboratory Director

DR. SHERIF A. NASR

Certificate Type

Certificate of Accreditation

Certificate Type Description

This is a CLIA certificate is issued to Siparadigm Llc on the basis of the laboratory's accreditation by an accreditation organization approved by CMS. This type of certificate is issued to a laboratories tha perform nonwaived (moderate and/or high complexity) testing.

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